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Vascular smooth muscle cells in intimal hyperplasia, an update

Sébastien Déglise, Clémence Bechelli, Florent Allagnat

Frontiers in Physiology · 2023 · Review · CC BY

doi:10.3389/fphys.2022.1081881

Abstract

Arterial occlusive disease is the leading cause of death in Western countries. Core contemporary therapies for this disease include angioplasties, stents, endarterectomies and bypass surgery. However, these treatments suffer from high failure rates due to re-occlusive vascular wall adaptations and restenosis. Restenosis following vascular surgery is largely due to intimal hyperplasia. Intimal hyperplasia develops in response to vessel injury, leading to inflammation, vascular smooth muscle cells dedifferentiation, migration, proliferation and secretion of extra-cellular matrix into the vessel’s innermost layer or intima. In this review, we describe the current state of knowledge on the origin and mechanisms underlying the dysregulated proliferation of vascular smooth muscle cells in intimal hyperplasia, and we present the new avenues of research targeting VSMC phenotype and proliferation.

Full text

From PubMed Central, U.S. National Library of Medicine, as current on Oct 27, 2026. Paragraph numbers are ours, so an answer can point at one.

1 Introduction

Intimal hyperplasia (IH) is a known complication of all types of vascular procedures, including arterial bypass, angioplasty, stenting, and endarterectomy. The progressive thickening of the vessel wall causes both an outward and an inward remodeling, leading to a narrowing of the vessel lumen, and eventually leads to impaired organ perfusion.

IH starts as a physiologic healing response to injury to the blood vessel wall. As such, the process of IH is initiated by endothelial cell (EC) injury. EC constitute the interface between the blood and the vessel wall, maintaining a non-thrombogenic surface and regulating the vascular tone (vasodilation and vasoconstriction). EC loss following surgery promotes vasoconstriction, platelet aggregation and recruitment/activation of resident and circulating inflammatory cells. The “activated” EC, recruited platelets and immune cells secrete cytokines and chemokines, which trigger a pro-inflammatory response. In addition, these cells secrete growth factors, including platelet-derived growth factor (PDGF), basic fibroblast growth factor (bFGF), transforming growth factor beta 1 (TGF-β) and thromboxane A2, which stimulate a number of intracellular signaling pathways in vascular smooth muscle cells (VSMCs) and fibroblasts. Together, the secretion of these factors and the loss of EC-derived gasotransmitters nitric oxide (NO) and hydrogen sulfide (H2S), promote vessel remodeling and reprogramming of cells composing the media and adventitia layers. This injury-induced phenotypic modulation of VSMCs promotes repair of the lesion, but failure to resolve the healing response leads to the formation of a neointima layer between the intima and the internal elastic lamina. This new layer is made of VSMC-like cells and extracellular matrix (ECM).

Despite decades of research and numerous clinical trials, IH remains a poorly-treated problem and a major contributor to restenosis following surgical revascularization. For open surgeries such as bypass and endarectomy, the rate of restenosis at 1 year between is 20%–30%. For endovascular approaches, the rate of secondary occlusion following balloon angioplasty and stenting ranges from 30% to 60%, depending on location. IH also occurs at anastomoses in fistula creation.

2 Vascular smooth muscle cells

VSMCs are the most abundant cells in vessels. Located in the media layer of the vessels, VSMCs are in constant crosstalk with ECs composing the intima, resident immune cells of the vessel wall, and other signal from the ECM. Unlike skeletal muscle cells, VSMCs have remarkable plasticity, sensing, adapting and influencing other cell types and their environment.

2.1 VSMC identity

In a mature blood vessel, medial VSMCs display a spindle-shaped contractile phenotype and express smooth muscle specific contractile proteins, including myosin heavy chain 11 (MYH11), calponin, smooth muscle 22α/transgelin (SM22α/tagln) and smooth muscle cell α-actin (ACTA2).

The differentiated contractile identity of VSMCs is ensured at the transcriptional level via the serum response factor (SRF) and the VMSC-specific transcription factor myocardin (MYOCD). SRF is a ubiquitous transcription factor binding to a general sequence motif in the CArG element (CC (A/T-rich) 6GG) to regulate the expression of marker genes. Myocardin is expressed specifically in cardiomyocytes and VSMCs, and acts as a potent coactivator of SRF and mediator of environmental cues to stimulate VSMC contractile genes. Two additional myocardin-related transcription factors (MRTF-A and B), homologous to MYOCD, form heterodimers with MYOCD to enhance transactivation of SRF. Unlike MYOCD, which is localized in the nucleus, MRTFs are sequestered in the cytoplasm through binding to G-actin monomers (Scheme 1).

2.2 VSMC reprogramming in IH

Unlike skeletal muscle cells, which are terminally differentiated, adult VSMC are highly plastic cells capable of profound phenotypic alterations in response to changes in their local environment. The ability of VSMCs to switch from a quiescent “contractile” phenotype to a proliferative “synthetic” phenotype is important for vascular injury repair. However, it also plays a complex role relevant to different pathological states, especially in the context of atherosclerosis and IH. The causal role of VSMCs plasticity in vascular remodeling during IH is undisputed. Upon vascular injury, the concerted endothelial dysfunction and immune response modulate core transcription factors driving a gene reprogramming toward ECM production and secretion, whereas the expression of the typical VSMC markers is reduced markedly. VSMCs switch to a “synthetic” phenotype, characterized by a loss of contractile markers, a transition to a rhomboid morphology, and a marked increase in proliferation, migration, and protein synthesis. Matrix remodeling is driven by increased expression of proteases such as matrix metalloproteinases (MMPs), Cathepsins, A disintegrin and metalloproteinases (ADAMs) and ADAM with thrombospondin motifs (ADAMTSs), and matrix-associated lysyl oxidase (LOX) and tenascin. In addition, “activated” VSMCs exhibit a pro-inflammatory phenotype, producing tumor necrosis factors alpha (TNFα) and monocyte chemoattractant protein-1 (MCP-1/CCL2), leading to positive feedback cascade of enhanced VSMC migration and proliferation. Those synthetic VSMCs then migrate from the medial layer to the vessel intima to form a neointima layer. Growth factors, cytokines and chemokines trigger VSMCs migration and proliferation via the MAPK, mTOR and Hippo signaling pathways (Scheme 2). Non-coding RNAs and epigenetic modifications further modulate the activity of these pathways in the context of IH. Below is a detailed account of the role and interplay of the main pathways involved in VSMC phenotype regulation in the context of IH. Below we describe the sequence of events and various pathways involved in VSMC reprogramming in IH.

2.2.1 Role of EC dysfunction

Located at the contact between the blood and the vessel wall, the EC maintain a non-thrombogenic surface and regulate the vasomotor activity (vasodilation and vasoconstriction) of vessels. In arteries, EC require high laminar shear stress to maintain proper function, i.e. secrete anti-coagulation and vasodilation agents, mainly prostacyclins and the gazotrasnmiters nitric oxide (NO) and hydrogen sulfide (H2S).

Endothelial dysfunction or injury following surgery results in loss of eNOS, the enzyme producing nitric oxide (NO) and impaired H2S production by cystathionine γ‐lyase (CSE). NO produced and released by EC plays an important role in maintaining the quiescent contractile features of VSMC. Briefly, EC-derived eNOS-dependent NO production promotes vasodilation and VSMC relaxation via increased cGMP production and PKG activation to reduce cytoplasmic calcium concentration. Loss of NO also leads to expression of adhesion molecules ICAM-1, VCAM-1 and P-selectin and secretion of chemokine MCP-1, which promote platelet aggregation and leukocyte chemotaxis. NO also promotes the expression of VSMC markers and inhibits VSMC proliferation and migration via cGMP-dependent and independent mechanisms [Reviewed in]. The study of eNOS-deficient mice also suggest that NO deficiency promotes recruitment of stem cell antigen-1+ (Sca-1+)/c-Kit−/Lin− SMC progenitor cells in a mouse model of carotid artery ligation.

H2S works in consort with NO, often providing redundant or substituting NO in some settings. Overall, the vascular effects of NO and H2S are mutually supporting and entangled, with both gasotransmitter having potent vasorelaxant, anti-inflammatory and anti-oxidant properties, and beneficial effect on the cardiovascular system [for full review see]. CSE expression and activity, as well as free circulating H2S, were reduced in patients suffering from vascular occlusive diseases and higher circulating H2S levels were associated with long-term survival in vascular surgery patients. Mice lacking CSE show a significant increase in IH formation as compared to WT mice in a model of carotid artery ligation. On the contrary, CSE overexpression decreases IH formation in a murine model of vein graft by carotid-interposition cuff technique. We and others demonstrated that several H2S donors inhibit IH in vivo in various models in rats, rabbits, mice, and in human great saphenous vein segments ex-vivo. H2S also directly inhibits VSMC proliferation and migration. In VSMC, H2S inhibits the MAPK pathway and mTOR pathway. H2S also limit MMP2 expression and ECMs degradation, reducing VSMCs migration. H2S also inhibit microtubule polymerization, leading to cell cycle arrest and inhibition of proliferation and migration in primary human VSMC. Taken together, reduced NO and H2S production promotes vasoconstriction, platelet aggregation, inflammation and leucocyte infiltration and oxidative stress.

The platelets and immune cells produce and secrete growth factors including PDGF-BB, bFGF, epidermal growth factor (EGF) and TGF-β. In addition, activated ECs secrete the stromal derived factor 1α (SDF-1α), which stimulates the recruitment of progenitor cells to the vessel wall. Activated ECs also release endothelin-1, which binds to the G-protein coupled receptors (GPCR) endothelin-1 receptor and transactivate pathologic growth factor signaling including PDGF-BB, bFGF, EGF, TGF-β and thromboxane A2.

2.2.2 Role of growth factors and the MAPK pathway

Originally, IH was thought to be driven by circulating cells, especially platelets, secreting platelet-derived growth factor-BB (PDGF-BB). It is now well established that VSMC proliferation is stimulated by the concerted action of several growth factors including PDGF-BB, as well as FGF, EGF and TGFβ. These growth factors mainly act via the mitogen-activated protein kinase (MAPK) pathways. The MAPK pathway, composed of extracellular signal-regulated kinases (ERKs), c-jun NH2-terminal kinases (JNKs), and p38MAPK, is induced by extracellular stress and regulates cell differentiation, growth and apoptosis. The growth factors PDGF-BB, FGF, EGF and TGFβ activate the MAPK cascade via the Ras/Raf/MEK/ERK pathway. Cytokines and other signals derived from oxidative stress are also strong activators of the MAPK pathway, especially JNK to regulate VSMC identity. Overall, the MAPK pathway play a central role in VSMC proliferation and migration, and a plethora of pre-clinical studies in the last 30 years reported successful inhibition of PDGF-BB-induced-ERK or p38 activation to limit IH, including statins, a number of small inhibitor peptides, and many active compounds derived from plants providing cardiovascular benefits, which will not be listed here.

Downstream of PDGF-BB, ERK induce the Kruppel Like Factor 4 (KLF-4), a pluripotency transcription factor absent in contractile VSMCs. KLF4 interferes with the SRF/MYOCD module by binding to G/C repressor elements, or by competing with SRF for CArG elements to disrupt CArG–SRF–MYOCD. Further in vitro studies showed that KLF4 is required to observe PDGF-BB-induced VSMC proliferation and inhibition of MYOCD-responsive genes. In vivo, full body Klf4 mutant mice exhibit delayed injury-induced repression of VSMC differentiation markers. However, Klf4-deficient mice displayed increased cellular proliferation in the media and IH. Therefore, the role of KFL4 in IH is likely more complex and context-dependent than in vitro studies suggested. SMC-specific Klf4 deletion using SM22α-Cre mice further revealed that Klf4 is required to maintain a population of Sca1+ progenitor VSMC in the adventitia, which may a role in adventitial remodeling upon vascular injury.

MAPK activation also triggers ternary complex factors (TCFs) of the ETS-domain family, such as the ETS domain-containing protein-1 (Elk-1) and TCF21. These factors then displace MYOCD and induce SRF-dependent transcription of early response growth genes, leading to dedifferentiation and proliferation. ERK-mediated phosphorylation of MYOCD impairs activation of SRF and activation of VSMC contractile gene. ERK-mediated phosphorylation of MRTF-A has also been shown to block its nuclear translocation in HeLa cells and NIH3T3 fibroblasts, which may further reduce MYOCD activity (Scheme 2).

2.2.3 Role of the TGF-β non-canonical pathway

The SMAD protein family, particularly nuclear factors Smad2 and Smad3, mediate canonical TGF-β signaling. Interestingly, the canonical TGFβ signaling via the suppressor of mothers against decapentaplegic (SMAD) transcription factors SMAD2 and SMAD3 promotes the expression of differentiation marker SM22α, SMMHC and ACTA2, via enhanced binding of SRF to CArG elements within the promoters of these genes. TGFβ also stimulates the RhoA/ROCK signaling pathway and MRTFs release. However, TGF-β release in the context of endothelium injury and matrix remodeling stimulate VSMC proliferation and IH [reviewed in ]. The deleterious effect of TGF-β in the context of IH is linked to activation of the non-canonical TGFβ signaling pathway via the MAPK and inhibition of the SMAD signaling pathway. The non-canonical TGF-β signaling pathway also enhances the production and secretion of ECM protein collagen and proteoglycans in VSMCs, thus promoting the fibrosis associate with IH. In human VSMCs, thrombin or endothelin-1 binding to GPCR have been shown to transactivate the TGFβ type 1 receptor, leading to increase production and secretion of ECM protein collagen and proteoglycans. TGFβ also stimulate PDGF-B expression, amplifying PDGF-BB signaling. Of note, SMAD3 and TCF21 may compete for the same binding site to either promote or inhibit the expression of contractile genes. Thus, MAPK-induced TCF21 displace SMAD to inhibit the expression of the contractile phenotype markers. A recent study in the context of atherosclerosis using SMC-specific Smad3 deleted mice further highlight Smad3 as a key protective transcription factor again the formation of atherosclerotic plaques and vascular calcification (Scheme 2).

2.2.4 Dual role of angiotensin-II signaling and GPCR singaling

Angiotensin-II (Ang-II) is the main vasoconstricting hormone and effector of the renin angiotensin aldosterone system. Ang-II drives VSMC contraction via binding to the type 1 Ang-II GPCR receptor (AT1R), leading to mobilization of calcium and activation of the myosin light chain kinase (MLCK) and ROCK-dependent inhibition of the myosin light chain phosphatase (MLCP). Over stimulation of the AT1R signaling in pathological conditions stimulates VSMC proliferation and hypertrophy through stimulation of the MAPK-ERK pathway. In addition, GPCR stimulation also transactivate growth factor receptor, including EGF receptor, PDGF receptor and FGF receptor [reviewed in ].

While still controversial, Ang-II binding to the type 2 Ang-II receptor (AT2R) receptor is thought to counteract AT1R signaling. AT2R signaling maybe responsible for Ang-II-mediated stimulation of MYOCD expression and its target genes αSMA and SM-MHC, and inhibition of VSMC proliferation. Ang-II may also inhibit VSMC migration through the AT2 receptor by increasing cellular fibronectin synthesis. The anti-proliferative effect of Ang-II on VSMC might also be related to the angiotensin peptides angiotensin 1–7 (Ang-1-7). Ang-1-7 is formed by the catalytic action of ACE2 on ANG II. Ang-1-7 also counterbalances AT1R signaling, promoting vasodilation. Ang-1-7 exert its action through the GPCR Mas, and to some extent, via binding to the AT2R. Mas is expressed in VSMC and Ang-1-7 has been shown to inhibit VSMC migration and proliferation, and MMP expression. The beneficial effect of Ang-II and Ang-1–7 on VSMC phenotype also occurs indirectly, via ATR2- and Mas- mediated enhanced NO production in EC. Accordingly, Ang-1–7 treatment has been shown to accelerate endothelium recovery and limit IH following arterial injury. Overall, Ang-II has a context-dependent dual role in the modulation of VSMC phenotype, similarly to TGF-β (Schemes 1, 2).

2.2.5 Role of cytokines/chemokines and the NF-κB signaling pathway

IH is associated with EC activation and inflammation. After the vascular injury, the secretion of inflammatory factors recruits inflammatory cells. Pro-inflammatory cytokines also change the structure of the extracellular matrix (ECM) to facilitate infiltration. Over the years, numerous reports demonstrated the role of various combination of chemokines and cytokines in the progression of IH, and a wide range of anti-inflammatory therapies have been proven to reduce IH in preclinical models. As mentioned earlier, cytokines and other signals derived from oxidative stress promote VSMC proliferation and migration, and IH, via stimulation of the MAPK pathway, especially JNK. Cytokines also stimulate the nuclear factor kappa B (NF-κB) pathway. NF-κB is a master regulator of pro-inflammatory genes, including cytokines and cell adhesion molecules. Upon nuclear translocation, NF-κB (p65) directly interacts with MYOCD to inhibit the formation of the MYOCD/SRF/CArG ternary complex in vitro and in vivo, promoting the synthetic phenotype. Interestingly and conversely, MYOCD can also dampen NF-κB activity. Several studies reported that NF-κB inhibition inhibits VSMC proliferation in vitro and IH in vivo (Scheme 2).

The pro-inflammatory cytokines TNF-α and IL-1α, secreted by macrophages/monocytes upon severe inflammation, play a central role in inflammation. In vitro studies established that IL-1α and β and TNFα stimulate VSMC migration and proliferation. TNFα deletion prevented IH in a model of carotid artery ligation, while IL-1 type 1 receptor deletion tended to develop less IH. Selective targeting of TNF receptors has also been shown to protect against IH. The deleterious effects of TNFα may be mediated by the triggering receptor expressed on myeloid cells (TREM)-1, which promotes VSMC inflammation, proliferation and migration, and is associated with in stent restenosis in patients.

In the context of atherosclerosis, excessive inflammation or failed inflammation resolution promotes atherosclerosis development. Blockade of IL-1β and its receptor have been shown to limit plaque formation. However, in a recent study using SMC-specific IL-1 receptor KO in ApoE−/− mice, Gomez et al. demonstrated that the positive effect of IL-1β on VSMC proliferation promotes the formation of a protective SMC/collagen-rich fibrous cap during late-stage atherosclerosis. Interleukin-18 blockade also inhibited IH in a rat model of vascular injury. MCP-1, expressed by macrophages, ECs and VSMCs upon arterial injury, and its receptor CC chemokine receptor 2 (CCR2), are also involved in VSMC proliferation and IH in pre-clinical models. The inflammatory mediator toll-like receptor (TLR)-4, which signals through the MAPK and NF-κB pathway, has also been shown to contribute to IH in various animal models. Finally, recent studies highlight the role of the NLRP3 inflammasome downstream of pro-inflammatory signals in VSMC phenotypic transformation and proliferation in hypertension and atherosclerosis. The NLRP3-inflammasome is a large multiprotein complex activating caspase-1, which produces IL-1β and leads to cell pyroptosis. The role of NLRP3 in IH has been mostly linked to EC dysfunction and increased EC permeability. Thus, the NLRP3 inflammasome is strongly induced in EC upon pro-inflammatory exposure, and inhibition of NLRP3 inflammasome improves EC recovery and limits IH in various models. Interestingly, it was recently shown that NLRP3 inflammasome activity in EC leads to horizontal transfer of IL-1β via extracellular vesicles, which promotes VSMC phenotypic transformation and IH. Further studies are required to test whether NRLP3 inhibition in VSMC specifically would protect against IH. In contrast, the anti-inflammatory cytokines IL-10 secreted mostly by M2 macrophages, was shown to promote angiogenesis and endothelium repair, thereby resolving inflammation and reducing IH following carotid artery denudation.

2.2.6 Role of the RhoA/ROCK module

Rock is the main effector of VSMC contraction via P-MLC activity, and thus play an important role in the contractile phenotype. Mechanical forces and interactions with the ECM stimulate the expression of contractile genes via integrins, which activate the RhoA/ROCK signaling pathway to stimulate polymerization of G-actin monomers in filamentous (F)-actin, thereby releasing MRTFs for translocation in the nucleus. Canonical TGFβ signaling also stimulates the RhoA/ROCK signaling pathway and MRTFs release, which enhances the transcriptional regulation of SRF and expression of the contractile gene.

However, excessive ROCK activity downstream of GPCR activity has been shown to be involved in the deleterious vascular effects of AngII and other GPCR ligands. Studies in vivo have shown that ROCK inhibition protects from various models of IH in rats and pigs. Mechanistically, ROCK has been shown to promote VSMC hypercontraction and inward remodeling, VSMC proliferation and migration, and infiltration of inflammatory cells in the vessel wall. In absence of myocardin or in response to mechanical strain and/or GPCR/TGFβ-activated RhoA signaling, the ROCK/SRF pathway promotes proliferation and myofibroblast differentiation.

Overall, the RhoA/ROCK, MAPK, and NF-κB pathways, downstream of mechanical strain and PDGF-BB, TGFβ and cytokines, integrates stress and growth signals resulting in VSMC proliferation and migration, and IH. However, no strategy based on inhibition of MAPK or NF-κB signaling limited IH in human trials, indicating that these pathways are not the sole responsible for VSMC proliferation and migration in IH.

2.2.7 Role of the mTOR pathway

The mammalian target of rapamycin complex 1 (mTORC1) is the main hub integrating signals from the environment to control protein and nucleotide synthesis, cell growth and metabolism. mTORC1 is regulated via amino acid abundance through the GCN2 complex, and via glucose through the AMPK. mTORC1 activation is also under the control of growth factors, in particular insulin and the insulin-like growth factor-1 (IGF-1). Similar to insulin, IGF-1 binds to the insulin receptor or the IGF-1 receptor (IGF1R), and stimulates the phosphatidylinositol-3-phosphate kinase (PI3K)/Akt pathway and inhibit the mTORC1 repressor module TSC. Downstream of mTORC1 activation, a cascade of phosphorylation of kinases such as p70 ribosomal protein S6 kinase (p70S6K) stimulates cell growth and protein synthesis. In pathological condition when the MAPK is active, IGF-1 promotes VSMC proliferation and migration and IGF-1 transgenic mice display increased VSMC proliferation and migration and IH following mechanical injury. Conversely, inducible IGF-1R deletion reduced the formation of neointima in a mouse model of vein graft. However, a recent study reported that the deleterious impact of IGF-1 on IH is probably mediated by binding to the insulin receptor, rather that the IGF1R (Scheme 2).

As the name implies, mTOR is the main target of Rapamycin, one of the two main molecules used in the clinics for the treatment of IH (see Section 3.1: current treatment of IH). Inhibition of mTORC1 by Rapamycin leads to G1-S cell cycle arrest, preventing VSMC proliferation and migration and IH. Forkhead box protein O4 (FoxO4) promotes VSMCs dedifferentiation by disrupting the SRF/myocardin complex. mTOR inhibits Akt2 signaling, thereby promoting nuclear translocation of FoxO4 to disrupt the SRF/myocardin complex. Inhibition of mTOR by Rapamycin rescues the VSMC phenotype (Scheme 1).

Recent studies also highlight a role of the late endosomal/lysosomal adaptor and MAPK and mTOR activator (LAMTOR/Ragulator) in the regulation of mTORC1 activity and IH. LAMTOR1 is a scaffold protein complex on late endosomes/lysosomes that serves as a point of convergence/integration of nutrient status and growth factor signaling. LAMTOR1 regulates mTORC1 signaling in response to amino acid concentrations. Liu et al. recently showed that Lamtor1 and mTORC1 signaling were significantly increased in a mouse model of arterio-venous grafting, and that SMC-specific Lamtor1 deletion prevented IH in vein grafts in vivo. In a related study, the same group demonstrated that platelet-derived microvesicles induced LAMTOR1 expression, and activated mTORC1 signaling to promote VSMC dedifferentiation in a model of mouse carotid intimal injury. In a recent study using inducible SMC-specific disruption of Tsc1 in mice, Li et al. showed that mTORC1 hyperactivity promoted the apparition of VSMC with a proteolytic phenotype overexpressing MMP2, leading to the formation of thoracic aorta aneurysms and dissections. These VSMC also expressed the macrophage markers Lgal3, as well as lysosomal associated membrane protein-2 (LAMP2), but not CD45, CD11b, CD68, and F4/80.

Recent studies also highlight a role of the phosphatase and tensin homologue (PTEN) in the regulation of VSMC phenotype and proliferation. PTEN is a lipid phosphatase working as a tumour suppressor genes via inhibition of the PI3K-AKT-mTOR pathway, which provides benefits against VSMC phenotype switch and proliferation. In addition, it was recently reported that PTEN translocate to the nucleus, where it binds to SRF to promotes SRF binding to the promoter of VSMC-specific genes such as a-SMA, SM-MHC and SM22α (scheme 1).

2.2.8 Role of the hippo YAP/TAZ pathway

The Hippo pathway is emerging as a key player in VSMC proliferation. The Hippo pathway is a central regulator of early stage development in embryogenesis, vital for organ growth control and tissue homeostasis. The mammalian Hippo complex consist of MST1/2, LATS1/2, and MOB1, which together regulate the transcriptional co-activators Yes-associated protein (YAP) and Transcriptional coactivator with PDZ-binding motif (TAZ). The Hippo pathway senses cell density via tight and adherens junctions, and mechanical forces via integrins, FAK and Rho/Rock signaling, to regulate the transcriptional coactivators YAP/TAZ. YAP/TAZ also integrates signals from growth factors signaling pathway and GPCR signaling. The activation of the Hippo pathway leads to MST and LATS1/2 kinases activation, which phosphorylates of YAP and TAZ, leading to their degradation. When the Hippo pathway is off, active YAP/TAZ translocate to nucleus to interact with transcription enhancer activation domain (TEAD) transcription factors (TEAD1-4). The YAP/TAZ-TEAD protein complex transcribes genes that control cell proliferation and cell fate.

YAP/TAZ is required for vascular development but suppressed in contractile VSMC and adult cardiomyocytes. A recent study using inducible SMC-specific YAP/TAZ-deficient mice showed that YAP/TAZ is required to maintain the differentiated contractile phenotype. It was also recently shown that YAP/TAZ deletion results in impaired hypertension-induced vascular adaptation, leading to formation of neointimal lesions, elastin degradation and adventitial thickening. Thus, YAP/TAZ is required for maintenance of vascular homeostasis. In vitro, overexpression of YAP or activation of YAP/TAZ by thromboxane A2 stimulated the synthetic phenotype and VSMC proliferation. Recent evidence indicate that pulsatile laminar flow turns on the Hippo pathway, thereby targeting YAP/TAZ for degradation. In contrast, Hippo is turned off and YAP/TAZ activity upregulated in rodent models of IH where laminar flow is disturbed. Moreover, YAP knock-down in a rat model of carotid balloon injury, and SMC-specific YAP deletion in a mouse model of carotid artery ligation, reduced injury-induced VSMC phenotypic switch and IH. Another recent study highlights the key role of YAP downstream of FAK and Rho/ROCK signaling in the deleterious effect of Osteoprotegerin, a secreted protein involved in atherosclerosis, vascular calcification and matrix degradation.

TEAD1 is also induced after vascular injury, and SMC-specific TEAD1 deletion inhibits IH in mice. Interestingly, in this study, they report that TEAD1 promotes mTORC1 activation. Studies in the context of cancer also highlight a cross talk between MRTF/SRF and YAP-TEAD to regulate invasion. Additional recent studies suggest further cross-talk between the Hippo and mTORC1 pathways via microRNAs and regulation of autophagy to control cell growth and proliferation [reviewed in ]. Overall, the YAP/TAZ-TEAD module seems to play a central role in vascular function and adaptation, and dysregulation of this pathway contributes to IH in several ways.

2.2.9 Modulation by non-coding RNA

A large number of studies also support a major role of non-coding RNAs in the regulation of VSMC phenotype. Non-coding RNAs interact with DNA, proteins, and other RNA molecules, thus acting as versatile modulators of major cellular processes. Thus, microRNA (miRNAs), long noncoding RNA (lncRNAs) and circular RNAs (circRNAs) expressed in VSMCs have been described to control VSMC phenotype switching, proliferation, migration and apoptosis. In this review, we will not list all the non-coding RNA that have been described to play a role in VSMCs. For this, we direct the reader to recent reviews focused only on non-coding RNAs.

Non-coding RNAs have been described to either protect or contribute to IH, depending on their profile of expression. Thus, non-coding RNAs that are absent in contractile VSMC but overexpressed in synthetic VSMC (miR-21, miR-146a, lnc NEAT-1) tend to promote the synthetic phenotype. Conversely, non-coding RNAs that are down-regulated in IH (miR-22, miR-24, miR-143/miR-145, miR-663, lnc GAS5) tend to promote VSMC differentiation when overexpressed. Many non-coding RNAs have been reported to modulate the MYOCD/SRF module, KLF4 and FOXO4. Thus, down-regulated non-coding RNA such as the miR-143/miR-145 cluster could play an important in maintenance of the contractile phenotype via modulation of KLF4 and MYOCD/SRF. Additional recent studies indicate that microRNAs regulate interactions between the Hippo and mTORC1 pathways to control cell growth and proliferation [reviewed in].

Non-coding RNAs also regulate VSMC apoptosis and survival pathways. Several miRNAs regulate PTEN expression in VSMCs, thereby influencing the PI3K/Akt/mTOR pathway (miR-26a, miR-21), cell proliferation and survival. Non-coding RNAs also regulate caspase activation, either through Bcl2-mediated regulation (miR-21, HIF1α-AS1), or through the tumor suppressor p53 (Linc-p21, circ-ANRIL, H19).

Other non-coding RNAs such as miR-29a/b/c, miR-195 and long non-coding RNA HAS-AS1 have been described to regulate ECM production and matrix remodeling. Recent evidence also suggest that miR-155-5p inhibition via STAT3 facilitates reticulocalbin 2-driven vascular calcification. Of importance, several miRNAs and long-non coding RNAs have been described to contribute to VSMC to VSMC cross-talk and communication between VSMC and EC or VSMC and platelets through horizontal transfer of non-coding RNAs via microvesicles or exosomes.

Many non-coding RNAs have been implicated in VSMC biology. However, many of these non-coding RNAs are not specific to VSMCs, and may have different roles in other tissues and pathologies. Dong et al. recently identified CARMN (cardiac mesoderm enhancer-associated noncoding RNA) as a highly abundant SMC-specific lncRNA downregulated in various vascular diseases. CARMN was further demonstrated to maintain the VSMC contractile phenotype both in vitro and in vivo by directly binding to MYOCD and potentiating MYOCD function.

The pleiotropic effects of non-coding RNA, together with their mobility and non-cell specificity, may limit their therapeutic potential. That said, they play a central role in response to pharmacological treatment and future strategies targeting VSMC phenotype and proliferation will need to take into account this complex network playing a key role in gene regulation.

2.2.10 Epigenetic modulation of VSMC identity

Gene expression is regulated at the chromatin level by epigenetic regulation, which refers to modifications in DNA or histones that shift chromatin accessibility. These include DNA methylation and post-translational modifications of histones (acetylation, methylation, phosphorylation, etc.). Recent evidence suggest that the phenotype of VSMC is also controlled via epigenetic modifications.

2.2.10.1 DNA methylation

DNA methylation is associated with chromatin condensation and gene repression. Once though irreversible and a sign of terminal cell differentiation, DNA methylation is now recognized as a dynamic process of de novo methylation, maintenance of the methylated cytosine, and demethylation. The DNA methyltransferase family (DNMTs) catalyzes DNA methylation. DNMT3A and DNMT3B are responsible for the de novo methylation. DNMT1 maintains DNA methylation pattern through cell replication. DNA demethylation occurs both passively and actively via the ten-eleven translocation methylcytosine dioxygenase (TET).

In 2013, Liu et al. showed that TET2 knockdown inhibits expression of MYOCD and SRF, with concomitant upregulation of KLF4, while TET2 overexpression was sufficient to induce a contractile phenotype. They further show that local viral-mediated Tet2 overexpression or knock-down at the site of injury in a mouse model of femoral wire injury reduced or increased IH, respectively. The authors propose TET2 as a master epigenetic regulator of VSMC differentiation. Interestingly, TET2 knockdown prevented rapamycin-induced VSMC differentiation, suggesting an interplay with mTORC1.

It was also shown that DNMT-1, the key DNA methyltransferase maintaining DNA methylation pattern, methylates and suppress the TET2 gene in VSMCs, thereby preventing TET2-mediated contractile gene demethylation. It was also recently shown that TET2 expression is under the control of non-coding RNA miR-22-3p and circMap3k5. Furthermore, Jeong et al. discovered that FAK, which is induced upon vascular injury, elicits VSMC dedifferentiation by stabilizing DNMT3A. They further show that FAK inhibition leads to DNMT3A degradation and DNA hypomethylation of contractile gene promoters, which increased VSMC contractile protein expression.

2.2.10.2 Histone acetylation

Histone acetylation is another epigenetic modification that opens the chromatin to facilitate transcription. Histone acetylation in governed by histone acetyltransferases (HATs) such as p300 and CREB-binding protein (CBP), which promote chromatin opening. Concersely, Histone deacetylases (HDACs) remove acetyl groups from lysine residues to close chromatin. HDAC hyperactivity is a hallmark of cancer and promotes cell proliferation. Recently, Chakraborty et al., demonstrated, using VSMC-specific knockout mice, that p300 and TET2 are mutually required to stimulate the expression of contractile markers, while CBP facilitates the recruitment of HDAC2 and 5 to contractile protein promoters to lock the chromatin.

Downstream of PDGF-BB, KLF4 may associate with HDAC2 on contractile gene promoters to repress their expression. PDGF-BB also increases HDAC4 expression and activity, and HDAC4 knockdown inhibits VSMCs proliferation and migration. In addition, HDACs have been describe to regulate non-histone proteins, including myocardin/MRTF, SRF, and KLF4. Thus, HDAC4 and HDAC5 suppress VSMC contractile gene expression via binding to MYOCD. HDAC6 sequesters MRTF-A in the cytosol, which facilitates PDGF-BB-induced repression of contractile genes.

2.2.10.3 Histone methylation

Gomez et al., showed that dimethylation of lysine 4 of histone H3 (H3K4me2) at the MYH11 locus is a hallmark of VSMC in human and mouse, which is kept even in atherosclerotic dedifferentiated VSMC with no detectable expression of VSMC marker genes. Another recent study further uncovered that H3K4me2 removal in VSMC is sufficient to induce the synthetic phenotype, due to impaired recruitment of TET2, leading to loss of miR-145 expression. Consequently, in vivo editing of H3K4me2 exacerbates VSMC plasticity and IH.

2.3.1 Contribution of VSMC

IH is probably, for the main part, formed by proliferating VSMC originating from dedifferentiated contractile medial VSMC. However, it is now well accepted that arterial and neointimal VSMCs are phenotypically heterogeneous and the origin and identity of the VSMC composing the neointima remains debated. Recent VSMC lineage tracing studies using in vivo cell fate tracing with SMC-specific genetic reporter tools suggest that previous single marker-based studies might have failed to identify VSMCs correctly. These new studies also question the multiple origin of neointimal cells, advocating for VSMC-derived multiple cell types present in atherosclerotic and neointima lesions. Multicolor lineage tracing further suggest that a small subset of VSMCs expand after injury to form clonal patches of neointimal cells. Further studies are required to elucidate the identity of this small subset of VSMCs. That said, a large body of literature still describes that neointimal may arise from other local or circulating cells.

2.3.2 Contribution of adventitial fibroblasts

In addition to medial VSMC-derived cells, neointimal-cells have been documented to have various origins. The most abundant, after medial VSMC, are probably myofibroblasts. Myofibroblasts originate from quiescent fibroblasts, the most common cell type in the adventitia, which have converted into proliferating fibroblasts expressing several VSMC markers such as α-SMA, SM-22α and calponin. These cells migrate into the media-neointima layer where they secrete pro-inflammatory cytokines, chemokines and altered ECM and metalloproteinase components. On the other hand, several studies in atherosclerosis using EC-lineage tracing have shown that endothelial-to-mesenchymal transitions (EndoMT) account for a large fraction of MSCs evolving into myofibroblasts. Thus, 20%–45% of myofibroblasts in atherosclerotic lesions would be of endothelial origin, and 20% of all EC express ACTA2 in ApoE−/− under high cholesterol diet. EndoMT may play an important role in atherosclerosis but the role and extend of EndoMT in IH remains uncertain. Further recent lineage study (see Section 2.3.4) question the origin of neointimal myofibroblasts.

2.3.3 Contribution of progenitor cells

Accumulating evidence also shows that neointimal cells may come from progenitor cells originating from the vessel wall, especially the adventitia layer. These studies support the existence of various populations of mesenchymal stem cells (MSCs) or multipotent vascular progenitor cells within the vessel wall. In 2004, Hu et al. were the first to characterize progenitor cells positive for Sca-1, c-kit and CD34 in the adventitia layer of ApoE−/− mice, and to demonstrate that these cells could differentiate into myofibroblasts and VSMC found in the intima layer of atherosclerotic lesion. Further studies identified similar progenitor cell populations in human arterial and venous tissue, suggesting a role for these cells in arterial remodeling and IH. In contrast, recent evidence suggest that Sca1 upregulation is a hallmark of VSMCs undergoing phenotypic switching in atherosclerotic plaques.

The cells composing the neointima may also arise from circulating progenitor cells or from the bone marrow. However, the contribution of circulating progenitor cells to IH seems to depend upon the model and the type of injury. In 2003, Tanaka et al. demonstrated that bone marrow cells contribute up to 50% of VSMC in the neointima in a model of wire-mediated endovascular injury. In contrast, they observed only a few bone marrow-derived cells in the neointima in a model of carotid artery ligation and almost no detectable cells in a model of perivascular cuff replacement. Similarly, studies in the atherosclerosis field yield conflicting results regarding the role of bone marrow derived cells in atherosclerotic VSMC (reviewed in details in]. Studies in human in the context of atherosclerosis using cross-sex bone marrow transplant also identify that 10%–20% of VSMC marker-positive cells in coronary artery lesions are of myeloid origin. However, most neointimal cells are likely of medial origin, as demonstrated with ex vivo studies using human vessels showing that IH forms in a vessel self-sufficient manner, independently of circulating factors or cells. Circulating progenitor and bone marrow-derived cells probably play a more important role in the endothelium repair than through direct contribution to the VSMCs composing the neointima. That said, a recent study using cell fate mapping and single-cell RNA sequencing identified Sca1+ vascular progenitors in the adventitial layer of artery walls. The authors show that these cells migrate into the medial layer where they proliferate as de novo VSMCs faster than medial VSMCs. Drawing conclusions from these studies remains challenging given the small number of studies and the variety of experimental models and methodology, especially the methods and markers employed to isolate and identify cell types.

2.3.4 Recent insight from lineage tracing studies

Recent VSMC lineage tracing studies using in vivo cell fate tracing with SMC-specific genetic reporter tools suggest that previous single marker-based studies might have failed to identify VSMCs correctly. Even though many classical VSMC markers such as αSMA and SM22α are problematic, MYH11 may remain a stable VSMC protein still present in VSMC-derived neointimal cells. Lineage tracing of bone marrow-derived progenitors in a model of femoral wire-induced injury revealed that circulating progenitors are recruited to injured vessels but do not differentiate into VSMC, but mostly to macrophages. Similarly, using a model carotid artery ligation, Herring et al. found that 80% of the neointimal cells derive from Myh11+ or Acta2+ cells. Additional studies in the context of atherosclerosis reported that 30%–70% of plaque cells originate from VSMC, while up to 80% of VSMC-derived cells in the plaques do not express the VMSC markers Acta2. It was further observed that about 7% of VSMC-derived cells are Sca1+ mesenchymal stem cells (MSCs) and 12% are Acat2+ Pdgfβr+ myofibroblasts-like cells, accounting for about 50% of the myofibroblasts-like cells found in the plaque. A recent study also highlights that neointimal cells arise from a small number of clonal Sca1+ dedifferentiated VSMC. These studies question the fact that myofibroblasts arise from adventitial fibroblasts. Further lineage tracing studies will be required to assess the contribution of medial VSMC to the population of myofibroblasts in the context of IH. Similarly, it seems that Sca1+ cells, usually referred to as MSCs, may have various origins. Originally, it was proposed that MSCs come from medial or adventitial resident or circulating progenitor cells, but it is now clear that some MSCs cells are dedifferentiated medial VSMC expressing the stemness marker Sca1. In contrast, myeloid-derived cells have be shown to express VSMCs markers, such as Sm22α and Acta2 in the context of atherosclerosis.

2.3.4.1 VSMC-derived neointimal cells may have a osteo-chondrogenic phenotype

In the context of atherosclerosis, lineage tracing identified VSMC expressing the macrophage markers CD68 and/or Lgals3, suggesting that some VSMCs may dedifferentiate in macrophage-like cells. However, recent single-cell RNA sequencing from murine atherosclerotic lesions in ApoE−/− with VSMC lineage tracing using Tagln and calponin suggest that Lgals3+ may be an early marker of phenotypic modulation towards fibroblast-like cells, which they term “fibromyocytes”, rather than into classical macrophages. Using a similar approach, Alancar et al. also observed that Lgals3 is a marker of an early transitional state of VSMCs with an ECM remodeling phenotype, which ultimately contribute to three populations of osteogenic and other pro-inflammatory non-macrophage VSMCs-derived cells. Other recent studies describe this intermediate multipotent cell type during atherosclerosis, which could differentiate into inflammatory cells and fibro/osteochondrogenic cells, as well as return toward the VSMC phenotype. Another recent study identified five VSMC-derived cell populations among CD45− cells in the atherosclerotic aorta of ApoE−/− under high cholesterol diet. Based on their gene expression profile, these were labelled macrophagic/calcific phenotype, mesenchymal/chondrogenic phenotype, inflammatory/fibro-phenotype and inflammatory phenotype. Of note, these cells all express KLF4, the main MYOCD/SRF disruptor and SMC-specific Klf4 knockout leads to marked reduction in Lgals3+ VSMC and reduced atherosclerotic plaques. Thus, Lgals3 might be a marker of stemness rather than a marker of macrophages. That said, some VSMC-derived cells do express traditional macrophage markers CD11b and F4/80, and have been shown to perform nonprofessional phagocytosis and contribute to the population of pro-inflammatory foam cells in atherosclerotic plaques. Among all these studies conducted in the context of atherosclerosis, one study was performed after partial carotid artery ligation in the mouse. This study identified 15 clusters 1-week post injury, among which four EC-derived cell populations involved in lipid metabolism and lipid storage, mechanotransduction or undergoing EndoMT transition. Of note, the study identified an intermediate VSMC population progressing into fibro/osteochondrogenic-like VSMCs. Pro-inflammatory cell were all of CD45+ origin. Osteo-chondrogenic differentiation of VSMCs contributes to vascular calcification in vascular diseases and this osteo-chondrogenic gene signature suggest that VSMC may transition towards osteoblast-like cells leading to vascular calcification. Vascular calcification plays a major role in arterial stiffness in peripheral artery disease, as well as in atherosclerosis, chronic kidney disease, hypertension, and diabetes. Vascular calcification begins as microcalcification near the internal elastic lamina, which progresses to calcified nodules. Reactive oxygen species and inflammatory mediators in the vessel wall, such as TNF-α, increase the expression of Msx2, which increases the expression of Runt-related transcription factor 2 (RUNX2), SOX9 and osterix. These transcription factors upregulate osteogenic markers such as osteopontin, osteocalcin, bone morphogenetic protein-2 (BMP-2), and alkaline phosphatase. Recent studies highlight a key role of VSMC-VSMC cross-talk in vessel calcification, via the release of exosomes carrying cargo such as mRNAs, miRNAs and peptides regulating the expression of osteogenic markers such as RUNX2 in the recipient cells. Of note, Gli1+ mesenchymal stem cells and circulating stem cells may also differentiate into osteoblast-like cells, and play a role in vessel calcification.

It should be noted that no study described macrophage-like VSMCs in the context of IH and studies suggest that inflammatory cells in IH mainly come from circulating CD45+ cells. It is unlikely that macrophage-like VSMC arise in neointimal lesion given that inflammation is transient in IH and IH lesion do not feature foam cells. New spatial transcriptomics techniques will also bring new understanding into the spatiotemporal regulation of VSMC fate, clonality, differentiation, and phenotypic modulation in the context of IH (Scheme 3).

2.3.4.2 Which pathways drive the osteo-chondrogenic phenotype?

Related to Section 2.2 of this review and the triggers of differentiation trajectories, current studies highlight a key of KLF4 upstream of Lgals3+. However, further studies will be required to determine the role and contribution of the MAPK, TGFβ, NF-κB, mTOR and YAP/TAZ pathways to the formation of different population of neointima VSMC-derived cells. The recent lineage studies underscore the enrichment of osteo-chondrogenic-like VSMCs in neointimal lesions. The canonical Wnt/β-catenin signaling pathway play a key role in osteogenesis and it has been shown to modulate Runx2 expression and VSMC osteogenic transdifferentiation and calcification. The TGF-β/BMP/SMAD pathway also regulate MSC differentiation during skeletal development, bone formation and bone homeostasis. However, its role as inducer of osteo-chondrogenic differentiation in VSMCs is more controversial. Thus, BMP2 stimulated osteogenic VSMCs differentiation in ApoE−/− mice, whereas BMP7 protected against vascular calcification in LDLR−/− mice. TGF-β promoted the chondrogenic phenotype in a mouse model of calcification via matrix Gla protein deletion. Conversely, SMC-specific deletion of TGF-β receptor 2 resulted in VSMC transdifferentiation into an MSC-like intermediate state that generated osteoblasts, chondrocytes, adipocytes, and macrophages in Apoe−/− mice. Of note, inflammation and the NF-κB signaling pathway have also been reported to drive osteogenic VSMCs differentiation in various models. In recent years, increasing evidence also suggest that mTOR plays important roles in the differentiation of mesenchymal stem cells (MSCs) into osteoblasts and chondrocytes. Thus, it is likely that mTOR pathways contribute to the formation VSMC-derived MSC and subsequent formation of myofibroblasts and osteo-chondrogenic-like VSMCs in the context of IH. In a recent study using inducible SMC-specific disruption of Tsc1 in mice, Li et al. showed that mTORC1 hyperactivity promoted the apparition of VSMC with a proteolytic phenotype overexpressing MMP2, leading to the formation of thoracic aorta aneurysms and dissections. These VSMC also expressed the macrophage/stemness marker Lgal3. Finally, the study of inducible SMC-specific YAP/TAZ-deficient mice showed that cytoplasmic YAP/TAZ inhibit nuclear translocation of Disheveled 3 (DVL3), which drives osteogenic transdifferentiation of VSMCs.

2.3.4.3 Limitations and future works

These new evidences underscore how little is known about the identity and origin of the cells responsible for the formation of IH. Recent single-cell RNA sequencing combined with VSMC lineage tracing led to new insights into VSMC phenotypic switching and evolution in the context of atherosclerosis. So far, these new techniques have been seldom used in IH models. Similar, but definitely different, differentiation trajectories probably occur during IH, with an enrichment in myofibroblasts and osteo-chondrogenic-like VSMC. Future studies using various models and human tissues will probably uncover more phenotype variations. The advent of new genetic tools has allowed inducible SMC-specific CRE recombination and VSMC tracing. However, all current promoters results in recombination in both vascular and visceral SMC lineages, which often lead to visceral myopathies. New Cre lines targeting VSMC-only would be useful to understand further the biology of VSMCs.

Several studies underscore that the origin of neointimal cells varies depending on the model. Thus, Roostalu et al. showed that in a model of wire-induced arterial injury, medial VSMCs were the primary contributors to IH. In contrast, supermicroanastomosis of the femoral artery around a nylon monofilament used as a stent resulted in early smooth muscle death and subsequent colonization of the vascular wall by adventitial cells and IH. Tanaka et al. also demonstrated that bone marrow cells contribute up to 50% of VSMC in the neointima in a model of wire-mediated endovascular injury, whereas only a few bone marrow-derived cells were found in the neointima in a model of carotid artery ligation, and almost no detectable cells in a model of perivascular cuff placement. In a recent study, Tang et al. also showed, in the context of femoral wire injury, that adventitial Sca1+ progenitor cells play an important role in VSMC expansion. These studies highlight that the origin and composition of IH probably differs between models and vascular bed, and depends on the level of damage to the media layer.

Of note, all cell-lineage evidence arise from mouse models of arterial injury whereas IH is strikingly different in rodent models and humans. In mouse models, IH develops as a VSMC-rich neointima with high proliferation rates in both the media and the neointima layers, and little ECM deposition. In contrast, IH ex vivo in human vein segments features extensive ECM remodeling and collagen deposition, accompanied by VSMC apoptosis and low VSMC proliferation. This morphology is more reminiscent of the lesions observed in patients who developed rapid restenosis following angioplasty or stent placement. These fundamental differences may explain, in part, why strategies targeting VSMC proliferation were successful to limit IH in pre-clinical models, but failed in human clinical trials. These differences may also explain the controversies regarding the origin, identity and role of the cells composing the neointima. Overall, the origin and nature of neointimal cells remains unclear and probably differs in mouse vs. human, in large vs. small arteries, and in venous graft vs. arterial injury.

3 Treatment of intimal hyperplasia

In this section, we review the current agents targeting VSMC proliferation and IH, their limitations, and new avenues of research aimed at VSMC-proliferation.

3.1 Current treatments

Numerous drugs have been tested over the years to limit restenosis. However, in most trials, the use of systemic drug therapy to prevent restenosis failed, due either to poor tolerance or lack of efficacy. The catheter-based endovascular interventions are taking advantage of the focal nature of atherosclerotic lesion and the plain old balloon angioplasties (POBA) and bare metal stents (BMS) strategies have revolutionized the management of vascular occlusive diseases. However, these devices suffered from high rates of in-stent restenosis (ISR) due to IH. To circumvent this problem, drug-coated balloons (DCB) and drug-eluting stents (DES) have been developed to reduce restenosis using local drug administration, which allows delivery of higher doses of drugs while minimizing systemic side effects. These medical devices are now the treatment of choice for endovascular approaches to treat short lesions in coronary or femoral arteries.

The most used drug is the anti-tumor chemotherapy Paclitaxel (Taxol™), a chemotherapeutic agent that stabilizes microtubule assembly by binding β-tubulin dimers, preventing their depolymerization. The low doses of paclitaxel in DES induce a cytostatic G1 cell cycle arrest, inhibiting proliferation and migration without inducing apoptosis. Several paclitaxel-coated balloons and eluting stents with various formulations and doses of paclitaxel demonstrated superiority to POBA or BMS.

Another drug used in DCB and DES is Rapamycin, also known as Sirolimus. Rapamycin inhibits the mammalian target of rapamycin complex 1 (mTORC1), a cellular sensor of amino acid abundance and growth factor signaling. mTORC1 is the main hub integrating signals form the environment to control protein and nucleotide synthesis, cell growth and metabolism, as well as proliferation and migration. Inhibition of mTORC1 by Rapamycin leads to G1-S cell cycle arrest, preventing VSMC proliferation and migration, and IH. In addition, Rapamycin promotes VSMC differentiation via Akt2 signaling, which drives FoxO4 export from the nucleus. Akt2 activation is also antiapoptotic and improves insulin sensitivity. Rapamycin also induces the master epigenetic regulator TET2 to stimulate VSMC differentiation. The pleiotropic effects of rapamycin on VSMC explains its efficacy and DES coated with Sirolimus and its analogs everolimus and zotarolimus are currently the preferred choice for coronary revascularization.

3.2 Limitations of current therapies

Although the rapamycin- and paclitaxel-eluting stents have improved outcomes compared with POBA and BMS, challenges remain. Overall, the arrival of DES and DCB reduced the incidence of restenosis below 10% in coronary arteries, but restenosis has been delayed rather than suppressed. DES also require prolonged antiplatelet therapy and hinder future surgical revascularization. In addition, the endovascular treatment of peripheral artery disease using DES is more complicated as rates of ISR after femoropopliteal artery stenting still range between 20% and 40% at 1 year. In peripheral below the knee small arteries, the use of DCB is controversial, and stents are not recommended due to the risk of thrombosis. Recently, various systematic review and meta-analysis questioned the widespread use of paclitaxel for the treatment of restenosis. Indeed, conflicting analysis identified or not an increased risk of all-cause mortality following application of paclitaxel‐coated balloons and stents in the femoropopliteal artery. These reports support the need to develop other approaches or use other molecules. In coronary interventions, Sirolimus is now the drug of choice for DES, and new devices are under evaluation to validate the use of Sirolimus-coated devices in below the knee peripheral arteries. Recent studies even report the safety and efficacy of biodegradable polymer Sirolimus-eluting stent.

Despite improved outcome with the latest generation of DES, the non-specific anti-proliferative effect of Paclitaxel and Sirolimus presents insoluble problems inherent to the nature of these molecules. As previously said, both compounds also inhibit EC proliferation, thus delaying re-endothelisation, which promotes clot formation and neo-atherosclerosis, and increases the risk of cardiovascular events. Additionally, their potent anti-proliferative effect are incompatible with systemic administration for more diffuse vascular diseases involving VSMC phenotypic switching, such as atherosclerosis.

3.3 New avenues of research

Numerous drugs have been tested over the years to limit restenosis, including several antiplatelet and anticoagulant drugs, calcium antagonists, lipid-lowering drugs, steroids, growth factor antagonists, and various antiproliferative agents. Since inflammation and oxidative stress have been both implied in IH, anti-inflammatory and anti-oxidant treatments were also tested to circumvent IH. Despite excellent pre-clinical results and promising initial reports, all failed to show significant effects or were abandoned due to side effects when tested in large, multicenter, randomized controlled trials. Thus, recent pre-clinical attempts using anti-inflammatory and anti-oxidant compounds to limit IH will not be discussed here. Currently, localized rapamycin-mediated inhibition of the mTOR pathway has proved beneficial via a numerous mechanism (see Section 3.1). Nevertheless, new avenues of research are pursued based on the latest discoveries. In this section, we highlight recent studies of the basic mechanisms that govern VSMC phenotype, which may provide new avenues to investigate for therapeutic intervention.

3.3.1 Clinical potential of the gasotransmitter hydrogen sulfide (H2S)

Hydrogen sulfide (H2S) is an endogenous gasotransmitter derived from the cysteine metabolism with important vasorelaxant, cytoprotective and anti-inflammatory properties. Its vasculo-protective properties have attracted a remarkable amount of attention. In this section, we review the potential clinical role of H2S to prevent IH.

Several studies highlighted the benefits of several H2S supplementation against IH in vivo in various models. We also showed that several H2S donors inhibit IH in human great saphenous vein segments ex-vivo. Recently, we demonstrated that Sodium thiosulfate (STS; Na2S2O3) works as a H2S donor to inhibit IH in vivo in a model of arterial IH, and ex vivo in human vein segments. Mechanistically, we showed that STS inhibits VSMC proliferation and migration via microtubules depolymerization. STS is already used in the clinic to treat cyanide poisoning and to increase the solubility of calcium for the treatment of acute calciphylaxis, a rare vascular complication of patients with end-stage renal disease. Sodium thiosulfate is also under test in a number of clinical trials for the treatment of ectopic calcification (NCT03639779; NCT04251832; NCT02538939). STS was also tested to reduce coronary calcium in patients receiving hemodialysis (NCT00568399). Interestingly, an ongoing clinical study aims to evaluate the efficacy and safety of STS compared to placebo on myocardial infarct size in ST-segment elevation myocardial infarction (STEMI) patients treated with percutaneous coronary intervention (NCT02899364). In light of the recent proposed role of osteo-chondrogenic phenotype of VSMC in IH, the fact that STS is also used in clinical pathology to reduce calcification is of particular interest.

Given that hypertension is a major risk factor for restenosis and that Angiotensin II stimulates VSMC proliferation (see Section 2.2.4), prospective studies were conducted to test the protective effect of ACE inhibitors (ACEi) against IH. Despite initial positive results with small monocentric studies, all human trials of ACEi and angiotensin receptor blockers have been inconclusive. We recently showed that Zofenopril, an ACEi and H2S donor combined, reduces IH in a genetic model of hypertensive mice. In addition, it suppressed IH in normotensive condition, where other non-sulfhydrylated ACEi (Enalapril, Lisinopril and Quinapril) had no effect. Furthermore, Zofenopril prevented IH in segments of human saphenous vein ex vivo. Mechanistically, H2S release from Zofenopril specifically reduced VSMC proliferation and migration via inhibition of the MAPK and mTOR pathways. Further studies should be conducted to test the therapeutic potential of this particular ACEi against IH.

The use of systemic drug therapy to prevent restenosis has been almost every time unsuccessfully because of narrow therapeutic ranges, side effects and/or diminished efficacy when administered systemically. The focal nature of IH lesions provide a window of opportunities for the use of local drug delivery using vascular medical devices. DCB and DES, as well as peri-adventitial drug delivery have been used successfully to limit IH, but strategies targeting VSMC proliferation only, while promoting endothelium recovery are needed to prevent IH. Unlike current non-specific cytostatic drugs, local H2S delivery might provide a unique opportunity to inhibit VSMC proliferation while promoting EC proliferation and endothelium repair. We recently developed a H2S-releasing biodegradable hydrogel to limit IH. This thiol-triggered hydrogel inhibited VSMC proliferation and IH in human vein segments more effectively than the sulfide salts (NaHS). Interestingly, this peptide hydrogel promoted HUVEC proliferation and transmigration in vitro, which may promote re-endothelisation, thereby supporting vascular repair. It was also shown that a locally applicable gel containing the H2S-releasing prodrug GYY4137 mitigates graft failure and improve arterial remodeling in a model of vein graft surgery in the mouse. We also recently demonstrated that STS, besides inhibiting VSMC proliferation and IH, promotes EC proliferation, VEGF-induced angiogenesis and neovascularization in vivo.

H2S works in consort with NO, and the vascular effects of NO and H2S are mutually supporting and entangled, with both gasotransmitter having direct and indirect effects on each other [for full review see]. All therapeutic strategies based on the use of the gasotransmitter NO have failed due to low tolerance and uncontrolled hypotensive effects. It will be interesting to see whether H2S-based solutions can succeed where NO failed. The first challenge will be to develop stable H2S-donor molecules allowing slow and sustained H2S release over the course of months/years. Such molecules are yet to be developed and will be hard to design given the reactivity of H2S. Eventually, H2S-releasing balloons and stents could provide much-needed device to limit VSMC proliferation while promoting EC recovery.

3.3.2 Targeting the YAP/TAZ-TEAD module

Emerging evidence suggest a major role of the YAP/TAZ-TEAD module is VSMC phenotype and proliferation/migration. Many molecules in development for cancer therapies inhibit YAP/TAZ/TEAD directly (Verteporfin, CA3, Super-TDU, Flufenamic acid) via dissociation of the YAP-TEAD interaction. The YAP inhibitor verteporfin suppress YAP-induced IH in a mouse model of arterial injury and Flufenamic acid inhibits the proliferation and migration of human aortic VSMCs in vitro. Further experiments are necessary to evaluate further the clinical potential of these drugs against IH.

GPCR inhibitors have also been describe to inhibit YAP/TAZ-TEAD indirectly. For instance, YM-254890, a specific G(α)q/11 inhibitor that indirectly inhibits YAP/TAZ, inhibited IH in a mouse model of vascular injury. However, YM-254890 also reduced systemic blood pressure and no further investigations were made in the context of IH.

Recent study also describe a stent eluting the Sp-1 inhibitor mithramycin A, which inhibited YAP and attenuated in-stent restenosis after rabbit angioplasty. Prostacyclin and thromboxane A2 also regulate vasorelaxation and vasoconstriction through GPCR. Interestingly, prostacyclin analogs stimulates YAP/TAZ phosphorylation and degradation, and inhibit TEAD-dependent VSMC proliferation and migration. In contrast, thromboxane A2 signaling activates YAP/TAZ to promote VSMC migration and proliferation in vitro. However, blockade of the thromboxane A2 receptor did not decrease IH in coronary angioplasty patients from the Multi-Hospital Eastern Atlantic Restenosis Trial (M-HEART II) clinical trial, suggesting that blocking YAP/TAZ is not sufficient to reduce IH in patients. In a recent study, Huang et al. described a Sorafenib-eluting stent, which inhibited in-stent restenosis in a rabbit carotid model, specifically through inhibition of YAP activity. Indeed, Sorafenib, a potent kinase inhibitor and anti-cancer molecule, seems to sequester YAP, thereby facilitating formation of the SRF/MYOCD complex and expression of VSMC-specific contractile genes. However, Sorafenib is a non-specific inhibitor of growth factor receptors known to impair EC proliferation and tumoral angiogenesis, which may impair endothelium repair and prolong the need for anti-thrombotic similarly to paclitaxel and Sirolimus.

Of note, other clinically established drugs probably target YAP/TAZ indirectly. Thus, the anti-diabetes drug metformin stimulate AMPK, which has been shown, in the context of cancer, to activate LATS1/2, thereby inhibiting YAP activity. Moreover, AMPK directly phosphorylates YAP Ser 94, a residue essential for the interaction with TEAD, thus disrupting the YAP-TEAD interaction. Although it has never been described to inhibit the YAP/TAZ/TEAD module in VSMC, Metformin has pleiotropic effect on VSMC, including inhibition of VSMC proliferation and vascular calcification. However, conflicting results have been reported regarding the effect of metformin on IH in vivo in rat models of arterial injury. Interestingly, Metformin reduce the rate of restenosis after percutaneous coronary intervention (PCI) in diabetic patients, independently of glycemic control. However, no large trials have been undertaken to specifically test the impact of metformin and other glucose lowering agents on restenosis in diabetic or non-diabetic patients. The cholesterol-lowering statins, which are potent inhibitors of IH, also inhibit RhoA, leading to LATS1/2- and MST1/2-independent YAP phosphorylation and degradation.

3.3.3 Targeting epigenetic regulators

As mentioned earlier, epigenetic modifications of VSMC genes, especially the MYOCD gene and SRF/MYOCD target genes, play an important role in VSMC phenotypic modulations. Several studies show that HDACs are upregulated in response to growth factors and by arterial injury [reviewed in (272)]. HDAC4 contributes to PDGF-BB-induced VSMCs proliferation and migration. Interestingly, in that study, HDAC4 targeting using the class IIa HDAC inhibitor MC1568 decreased IH in a mouse model of carotid ligation. Selective inhibition of HDAC6 using tubastatin A enhanced the nuclear activity of SRF via increased translocation of MTRF-A, thereby preventing VSMC dedifferentiation in vitro and IH in vivo. Similarly, Scriptaid, a potent pan HDAC inhibitor, decreases IH in a mouse model of arterial injury. In contrast, several studies showed that the pan HDAC inhibitor trichostatin A stimulates Akt-dependent VSMC proliferation and IH. Obviously, further pre-clinical studies are required before testing HDAC inhibitors in human cardiovascular disease.

Another interesting strategy to reduce IH would be to increase TET2 expression. Indeed, TET2 overexpression is sufficient to induce a contractile phenotype and local viral-mediated TET2 overexpression at the site of injury in a mouse model of femoral wire injury reduced IH. Pharmacological avenues to induce TET2 include vitamin C, which works as a cofactor to promote TET2 activity and demethylation. The other co-factors of TET2 Fe(II) and 2-oxoglutarate, or its close metabolite α-ketoglutarate, could also be used to increase TET2 activity. Thus, Vitamin C, as a cofactor of TET enzymes, increases 5hmC formation and promotes DNA demethylation and probably genomic stability, in addition to its antioxidant properties. Given the role of oxidative stress in IH, several clinical trials have assessed whether ascorbic acid (vitamin C) could limit restenosis over the years. Unfortunately, these studies usually reported modest effects of vitamin C on the incidence of restenosis. In the multivitamins and Probucol (MVP) large study, a combination of antioxidant Probucol, vitamins C and E and beta-carotene showed promising results against restenosis after angioplasty. However, Probucol was removed from the market because of concerns about its potential QT-prolongation and pro-arrhythmic effects. That said, given that Vitamin C is inexpensive and safe, further studies should be conducted to assess its potential against restenosis. Interestingly, Vitamin C promotes EC proliferation while inhibiting VSMC proliferation. This property alone warrants further investigations into the development of stents and balloon releasing Vitamin C, probably in combination with more potent VSMC inhibitors.

It was also shown that the DNA methyltransferase DNMT-1 suppress the TET2 gene in VSMCs, so DNMT-1 inhibitors could prove useful to increase TET2 activity. In that study the DNMT inhibitor 5-aza-2’-deoxycytidine reduced IH in a mouse model. However, the covalent DNMT1 inhibitors 5-azacytidine and decitabine, which are widely used in research to reduce DNA methylation levels, are rapidly cytotoxic. Thus, DNMT-1 inhibitors have limited translational potential. Interestingly, TET2 knockdown prevented rapamycin-induced VSMC differentiation, suggesting that TET2 is required for the effect of Rapamycin and thus an indirect target of Rapamycin. It was also recently shown that TET2 expression is under the control of non-coding RNA miR-22-3p and circMap3k5, so that non-coding RNA therapies targeting TET2 may be useful in the future. Again, the development of stents or balloons releasing epigenetic modulators able to revert the synthetic phenotype could provide new device to limit IH and restenosis.

4 Conclusion

As highlighted in this review, there is still a lot to learn about the mechanisms governing VSMC phenotype in native vessels and in the context of cardiovascular diseases. Recent advances in genetic tools, single cell and spatial omics allow, for the first time, to dissect the molecular signature of single cells and carry out detailed and precise analyses of VSMC dynamics in health and disease. So far, single cell RNA seq has only been used in the context of atherosclerosis with a sharp focus on immune cells, rather than VSMC. It will be interesting to see single cell RNA seq data in various model of IH. That said, single cell RNA seq is descriptive, does not allow lineage tracing, and entails loss of spatial information about the distribution of the subpopulations of cells. New techniques of spatial transcriptomic combined with multiplexed imaging are required to deepen our understanding of VSMCs in the context of IH. Such studies should be conducted in various models of IH as the origin and phenotype neointimal VSMC probably differ depending on the type of intervention, location, type and severity of injury.

VSMCs remain a target of choice for the treatment of IH and phenotypic reversal is a crucial point to prevent IH. The current approaches used to prevent IH only address VSMC proliferation, not their phenotypic identity, although both are linked closely. The main issue with current therapies is the nonspecific effect of paclitaxel and Sirolimus on cell proliferation, which requires targeted delivery and has deleterious effects on the endothelium. Moreover, DES are efficient in coronary arteries, but perform poorly in the peripheral vasculature. Therefore, other VSMC-targeted approaches are required. Understanding the spatiotemporal regulation of VSMC fate, clonality, differentiation, and phenotypic modulation will reveal mechanisms essential to discovering novel therapeutic candidates. Continued efforts on multiple fronts are necessary to translate these targets into viable cardiovascular therapies. Given the complexity of disease presentation and comorbidities, combining local delivery and systemic oral drug administration will likely be necessary to treat IH, as well as diffuse vascular pathologies such as atherosclerosis and vascular calcification. Another challenge for either systemic or local release reside in the delivery system. The development of DCB and DES releasing paclitaxel or Sirolimus led to innovative delivery systems. Gels, nanoparticles, multiple-layer coatings and biodegradable scaffolds are being developed to allow sustained drug release. It will be interesting to combine these delivery systems with new molecules.

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    Huang C. Zhao J. Zhu Y. (2020 ). Drug-eluting stent targeting sp-1-attenuated restenosis by engaging YAP-mediated vascular smooth muscle cell phenotypic modulation. J. Am. Heart Assoc. 9 (1), e014103.

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    Iwata H. Manabe I. Fujiu K. Yamamoto T. Takeda N. Eguchi K. (2010 ). Bone marrow-derived cells contribute to vascular inflammation but do not differentiate into smooth muscle cell lineages. Circulation 122 (20), 2048–2057.

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    Yu O. M. Miyamoto S. Brown J. H. (2016 ). Myocardin-related transcription factor A and yes-associated protein exert dual control in G protein-coupled receptor- and RhoA-mediated transcriptional regulation and cell proliferation. Mol. Cell Biol. 36 (1), 39–49.

    Not in our library10.1128/mcb.00772-15

  270. 270.

    Yuan X. Bhat O. M. Samidurai A. Das A. Zhang Y. Li P. L. (2020 ). Reversal of endothelial extracellular vesicle-induced smooth muscle phenotype transition by hypercholesterolemia stimulation: Role of NLRP3 inflammasome activation. Front. Cell Dev. Biol. 8, 597423.

    Not in our library10.3389/fcell.2020.597423

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    Yue X. Rao A. (2020 ). TET family dioxygenases and the TET activator vitamin C in immune responses and cancer. Blood 136 (12), 1394–1401.

    Not in our library10.1182/blood.2019004158

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    Zeng Z. Xia L. Fan X. Ostriker A. C. Yarovinsky T. Su M. (2019 ). Platelet-derived miR-223 promotes a phenotypic switch in arterial injury repair. J. Clin. Invest. 129 (3), 1372–1386.

    Not in our library10.1172/jci124508

  273. 273.

    Zeng Z. Xia L. Fan S. Zheng J. Qin J. Fan X. (2021 ). Circular RNA CircMAP3K5 acts as a MicroRNA-22-3p sponge to promote resolution of intimal hyperplasia via TET2-mediated smooth muscle cell differentiation. Circulation 143 (4), 354–371.

    Not in our library10.1161/circulationaha.120.049715

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    Zhang Q. J. Goddard M. Shanahan C. Shapiro L. Bennett M. (2002 ). Differential gene expression in vascular smooth muscle cells in primary atherosclerosis and in stent stenosis in humans. Arterioscler. Thromb. Vasc. Biol. 22 (12), 2030–2036.

    Not in our library10.1161/01.atv.0000042206.98651.15

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    Zhang L. N. Wilson D. W. da Cunha V. Sullivan M. E. Vergona R. Rutledge J. C. (2006 ). Endothelial NO synthase deficiency promotes smooth muscle progenitor cells in association with upregulation of stromal cell-derived factor-1alpha in a mouse model of carotid artery ligation. Arterioscler. Thromb. Vasc. Biol. 26 (4), 765–772.

    Not in our library10.1161/01.atv.0000207319.28254.8c

  276. 276.

    Zhang L. Sivashanmugam P. Wu J. H. Brian L. Exum S. T. Freedman N. J. (2008 ). Tumor necrosis factor receptor-2 signaling attenuates vein graft neointima formation by promoting endothelial recovery. Arterioscler. Thromb. Vasc. Biol. 28 (2), 284–289.

    Not in our library10.1161/atvbaha.107.151613

  277. 277.
  278. 278.

    Zhao G. Xu M. J. Zhao M. M. Dai X. Y. Kong W. Wilson G. M. (2012 ). Activation of nuclear factor-kappa B accelerates vascular calcification by inhibiting ankylosis protein homolog expression. Kidney Int. 82 (1), 34–44.

    Not in our library10.1038/ki.2012.40

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    Zhao J. Liu Z. Chang Z. (2021 ). Osteogenic differentiation and calcification of human aortic smooth muscle cells is induced by the RCN2/STAT3/miR-155-5p feedback loop. Vasc. Pharmacol. 136, 106821.

    Not in our library10.1016/j.vph.2020.106821

  280. 280.

    Zhou Y. Wang J. Y. Feng H. Wang C. Li L. Wu D. (2014 ). Overexpression of c1q/tumor necrosis factor-related protein-3 promotes phosphate-induced vascular smooth muscle cell calcification both in vivo and in vitro. Arterioscler. Thromb. Vasc. Biol. 34 (5), 1002–1010.

    Not in our library10.1161/atvbaha.114.303301

  281. 281.

    Zhu B. Zhao G. Witte D. P. Hui D. Y. Fagin J. A. (2001 ). Targeted overexpression of IGF-I in smooth muscle cells of transgenic mice enhances neointimal formation through increased proliferation and cell migration after intraarterial injury. Endocrinology 142 (8), 3598–3606.

    Not in our library10.1210/endo.142.8.8331

  282. 282.
  283. 283.

    Zhuang J. Luan P. Li H. Wang K. Zhang P. Xu Y. (2017 ). The yin-yang dynamics of DNA methylation is the key regulator for smooth muscle cell phenotype switch and vascular remodeling. Arterioscler. Thromb. Vasc. Biol. 37 (1), 84–97.

    Not in our library10.1161/atvbaha.116.307923

  284. 284.

    Zindel D. Mensat P. Vol C. Homayed Z. Charrier-Savournin F. Trinquet E. (2021 ). G protein-coupled receptors can control the Hippo/YAP pathway through Gq signaling. FASEB J. 35 (7), e21668.

    Not in our library10.1096/fj.202002159r

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    Zuckerbraun B. S. McCloskey C. A. Mahidhara R. S. Kim P. K. Taylor B. S. Tzeng E. (2003 ). Overexpression of mutated IkappaBalpha inhibits vascular smooth muscle cell proliferation and intimal hyperplasia formation. J. Vasc. Surg. 38 (4), 812–819.

    Not in our library10.1016/s0741-5214(03)00427-0

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