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Transport of Amino Acids Across the Blood-Brain Barrier

Rosa Zaragozá

Frontiers in Physiology · 2020 · Review · CC BY

doi:10.3389/fphys.2020.00973

Abstract

The blood-brain-barrier (BBB) present in brain capillaries, constitutes an essential barrier mechanism for normal functioning and development of the brain. The presence of tight junctions between adjacent endothelial cells restricts permeability and movement of molecules between extracellular fluid and plasma. The protein complexes that control cell-cell attachment also polarize cellular membrane, so that it can be divided into luminal (blood-facing) and abluminal (brain) sides, and each solute that enters/leaves the brain must cross both membranes. Several AA transport systems with different distribution in both sides of the BBB have been described. In a broad sense, at least five different systems of facilitative transporters, and all of them are found in the luminal membrane. Some of these transporters are very specific for a small group of substrates, and are located exclusively on the luminal side of the BBB. However, the two major facilitative carriers, system L and system y+, are located in both membranes although asymmetrically. The position of these Na+-independent transporters ensures AA availability into the brain and also its bidirectional transport across the endothelia cells. On the other hand, there are several Na+-dependent transport systems that will transport AAs against its concentration gradient together with the movement of Na+ ions. The majority of these active tranporters are present exclusively at the abluminal membrane, being responsible of amino acid efflux from the brain into the endothelial cells. Since those are Na+-coupled, the sodium pump Na+/K+-ATPase is also highly expressed in this abluminal side of the BBB. Once inside the cell the facilitative transporters located in the luminal membranes will mediate export from endotehial cell to blood. In summary, the polarized distribution of those transport systems between the luminal and abluminal membranes, and the fact that more than one transporter may carry the same substrate ensures supply and excretion of AAs in and out of the brain, controlling its homeostasis and proper function.

Full text

From PubMed Central, U.S. National Library of Medicine, as current on Oct 22, 2026. Paragraph numbers are ours, so an answer can point at one.

The Blood Brain Barrier

The term blood–brain barrier (BBB) was used to describe the unique characteristics of the microvasculature of the central nervous system (CNS). Such vessels within the CNS are continuous and non-fenestrated capillaries; moreover, endothelial cells (ECs) within the BBB are held together by continuous interendothelial tight junctions that limit paracellular transport across the endothelium. In fact, tight junctions of ECs give rise to a polarized cell composed of two distinct luminal (blood-side) and abluminal (brain-side) surfaces. Each of these membranes is made up of different lipids and intrinsic proteins (e.g., transporters) existing on the luminal and abluminal sides, that regulate movement of molecules between the blood and the brain.

Nevertheless, endothelial cells forming the BBB are not the only mediators of this function. Regulation of this process does not only involve the EC tight junctions. There are mural cells surrounding the ECs that form the walls of capillaries. These mural cells, located on the abluminal side of the EC layer, include vascular smooth muscle cells around the large vessels, astrocytes and pericytes, which are embedded in the basement membrane and cover the abluminal side of the endothelial wall with their processes. Several pericyte-endothelial cellular adhesions have been identified and due to the presence of contractile proteins within pericytes, these cells may control capillary diameter and thus blood flow. In fact, these cells have been shown to be important for regulating the formation of the BBB during development, as well as maintaining its function in adulthood and aging. Astrocytes are a major glial cell type, and their end-feet processes surround blood vessels and establish a neurovascular link, regulating blood flow in response to neuronal activity.

The basement membrane, composed of collagen type IV, laminin, fibronectin and heparan sulfate proteoglycan, separates ECs from other cellular members interacting with them. These interactions are essential for barrier formation and maturation during development and are maintained thereafter. However, barrier function is not solely regulated by ECs, pericytes, astrocyte-processes and basement membrane. Neurons, microglial cells and perivascular macrophages also influence the BBB and thus a more extended term, neurovascular unit, was coined to include all these elements. The relationships between different cell types allow for paracrine modulation which, in turn, regulates CNS homeostasis, such as BBB permeability and blood flow.

Transport Across the BBB

Cerebral capillary ECs differ from other ECs in that they have a larger number of tight junctions between neighboring cells, fewer cytoplasmic vesicles and higher amounts of mitochondria. The tight junctions limit paracellular movement and divide the membranes of ECs into two distinct sides with different membrane composition. In addition, transcellular flux is also restricted, as these ECs show extremely low transcytotic activity. Thus, molecules must pass two sheaths of membrane to enter or leave the brain so that transporters located on each side of the cell membrane play a pivotal role in controlling this movement. In this regard, the higher amount of mitochondria in these cells contributes toward generating more ATP molecules to drive the ion gradients which are critical for transport functions. All in all, the combination of physical barrier properties, together with specific transporters to deliver required nutrients, allows the ECs to tightly regulate CNS homeostasis. Several approaches have been undertaken to elucidate the different transporters, their expression and specific location. For example, isolation of brain microvessels and further genomic and proteomic analysis may permit the identification of the cellular location of proteins expressed within the neuro-vascular unit [for a review, see ].

Ultimately, transport across the BBB is an important step in the regulation of nutrient and metabolite movement between blood and the brain. Endothelial cells show a complex network of specific transporters present in one or both cell membranes (luminal and abluminal) to regulate this flow. It is the combined characteristics of both membranes that determine which molecules traverse the BBB and how fast. In fact, there are 244 genes belonging to the SLC (solute carrier) superfamilies that are expressed in brain microvessels, including slc2a1(glucose), slc16a1 (lactate, pyruvate), slc7a1 (cationic amino acids), and slc7a5 (neutral amino acids, L-DOPA). This paper gives an overview of these SLC transporters specific for AA transport, precisely pinpointing their polarized location, their substrates and their direction of transport.

Amino Acid Transporters

The concentration of AAs in brain extracellular fluid and cerebral spinal fluid is at least tenfold lower than plasma concentrations. The only exception to this being glutamine, the concentration of which is similar at both sides of the BBB. This gradient, as well as AA transport across the BBB is tightly regulated by AA transporters present in both membranes of ECs; in fact, ten AA transport systems with different membrane distribution have been reported (for localization of these transporters, see Figures 1 and 2).

In a broad sense, these transporters can be classified according to their presence in the luminal or abluminal membranes, or in both. Depending on the transport mechanisms used, these AA transporters can be antiporters, which exchange some AAs for others across the membrane by means of facilitative transport. On the other hand, symporters co-transport AAs together with ions along the electrochemical gradient of the ions and are active transporters. Five active transporters that require Na+ are present in the abluminal membrane and are responsible for the AA efflux from the brain into the ECs and from there to the blood. Furthermore, facilitative-carriers, which are sodium-independent, are located either in the luminal side or in both luminal and abluminal membranes (see Tables 1 and 2 for names, substrates and location of each transporter).

Facilitative Transport Across the BBB: Transporters Present in Both Membranes

Two sodium independent transport systems, LAT1 or L, and y+, mediate the facilitated exchange of large neutral AAs (both systems) and basic AAs (y+) in both luminal and abluminal membranes of ECs. They play a key role in delivering dietary essential neutral and basic AAs that cannot be synthesized within the brain (;; Figure 1).

Large Neutral Amino Acid Transporters

Neutral AAs are transported across the plasma membrane by proteins that belong to the solute carrier families SLC1, SCL7, SLC38 and SLC43. Of these SLC families, only SLC7 and SLC43 are Na+-independent and belong to system L amino acid transporter (system LAT), while SLC38 (Systems A and N) and SLC1 (System ASC) are Na+-dependent transporters and will be discussed further on. Early studies in vivo on transport across the BBB revealed that neutral AA moved from blood to brain by facilitative Na+-independent transport by means of a transmembrane transporter known as LAT1 (from system L amino acid transporter). LAT1 is encoded by the slc7a5 gene and forms a heterodimeric complex with the glycoprotein 4F2hc (CD98, SLC3A2) associated by a disulfide bridge. Recently, it has been shown that LAT1 is in charge of AA transport, whilst 4F2hc heavy subunit acts as a molecular chaperone that directs LAT1 to its definitive localization in the cellular membrane.

This transporter is highly expressed in the ECs of the BBB. Regarding polarity, LAT1 is present in both membranes in a 2:1 ratio (luminal vs. abluminal). A computational study supports the hypothesis that there is an asymmetry in either bi-directional kinetics and/or expression of LAT1 in brain ECs which in turn results in a functional polarity for these large neutral AAs transported by LAT1.

At the BBB, LAT1 is stereospecific (L > D), catalyzes an exchange (in 1:1 stoichiometry) of two AAs and is inhibited by BCH [2-aminobicyclo-(2,2,1) heptane-2-carboxylic acid], an amino acid-related compound that has been used as a selective inhibitor of the system L amino acid transporters. It preferentially transports branched AAs, and their substrates including Phe, Trp, Leu, Ile, Met, His, Tyr, Val and Thr, most of which are essential AA. Gln has also been described as a substrate for this transporter; however, Gln transport is not completely inhibited by BCH, suggesting that Gln has an additional Na+-independent transport system in the BBB, most likely system n. It has also been demonstrated that LAT1 shows different affinities on extracellular vs. intracellular sides; indeed, it has higher affinity for intracellular amino acids whose concentration controls the transport rate. According to this, L-leucine, L-isoleucine and L-methionine are better substrates for cellular efflux than influx to the cell.

LAT1 imports large and neutral amino acids in exchange for intracellular AAs (e.g,. glutamine), therefore it seems to be the most important path for neutral essential AAs to enter the brain. The homeostasis of these neutral AAs (which are asymmetrically distributed in plasma and brain) is essential, since some of them play a crucial role as precursors for neurotransmitters, such as dopamine, serotonin and histamine.

Cationic Amino Acid Transporter: System y+

The concentration of cationic amino acids (CAA; lysine, arginine, and ornithine) in ECF is 10–30% that of plasma although their transport across the BBB is less well known. Two families of proteins have been described as CAA transporters: CAT or cationic amino acid transporters system y+ (SLC7A1-4), which is selective for basic AA (index “ + ”); and BAT or broad substrate amino acid transport systems (that include B0,+, b0,+, and y+LAT2), which also transport neutral amino acids (index “0”). Transporter system B0,+ (or ATB0,+) is a symporter with 2Na+ and 1Cl–, therefore it will be discussed in the Na+-dependent transporters section. Indeed, it is the only Na+-dependent carrier that transports CAA. On the other hand, the presence of the Na+-independent systems b0,+ and y+LAT2 in either membrane of the BBB remains to be elucidated. Moreover, the Arg/Gln exchanger y+LAT2 (SLC7A6) appears to be expressed in the cerebral capillary endothelial cells in human in vitro BBB models, or even after ammonia treatment in cultured rat ECs. However, there is no information concerning its specific localization in the brain endothelium in vivo.

Furthermore, system y+ (CAT1, CAT2B and CAT3) seems to be the primary CAA transporter of the BBB; it has been known to be present in the luminal side since the early 1990s. More recent studies with enriched luminal and abluminal vesicles from the bovine BBB demonstrated that transporters from system y + also exist on the abluminal membrane. In fact, their activity is greater on the abluminal membrane and they are voltage-sensitive. Although CAT1 is the best characterized cationic AA transporter, other members have also been studied in the brain. CAT2 is expressed in the brain, but does not appear to be enriched at the BBB, since mRNA levels are <10% of that of CAT1. CAT3 is highly expressed in the brain and readily discriminates between L-lysine and L-arginine (difference of approximately 2-fold).

CAT1 (SLC7A1) has a higher affinity for Arg compared to the other CAA and is responsible for blood-to-brain transport of Arg across the BBBs. Since CAT1 forms a caveolar complex with endothelial nitric oxide synthase (eNOS), CAT1 is probably the most important player in providing Arg for NO synthesis in endothelial cells. Despite being primarily a CAA transporter, system y+ also exhibits weak interactions with neutral AA in the presence of sodium. In the BBB, this system may transport several NAA, both essential (Phe, Thr, His, Val, and Met) and non-essential (Ser, Gln, Ala, and Gly) although with much less affinity than system LAT1.

Facilitative Transport Exclusively Found on the Luminal Side

There are at least three different Na+-independent facilitative carriers found at the luminal membranes of ECs. These transporters that do not require energy for the movement of their substrates are not as abundant as the previously mentioned LAT and y+ systems. Indeed, they do not account for the movement of a large group of AAs but for specific molecules instead. Accordingly, these carriers regulate the efflux from the brain to plasma of glutamine and acidic AAs, mainly glutamate which can be neurotoxic at high levels. On the other hand, cysteine needs to be imported from plasma into the brain in order to synthetize glutathione (GSH), and this import is mediated by system XC– (Figure 1).

Glutamine Transporter: System n

L-glutamine (Gln) is the most abundant AA in plasma and cerebrospinal fluid and is a precursor for the main central nervous system excitatory (L-glutamate) and inhibitory [γ-aminobutyric acid (GABA) neurotransmitters]. Multiple transporters have been identified that are capable of glutamine transport, at both surfaces of the BBB. These include Na+-dependent transporters that belong to systems N, A, ASC, B0,+, and y+LAT2, and Na+-independent transporters from systems L, b0,+ and n.

Despite its potential importance, the mechanisms of Gln transport across the BBB and the polarity of these transporters has not been fully elucidated. What is certain is that Gln moves from the plasma across the BBB by a facilitated process. Initially, it was assumed that Gln was transported across the BBB on the neutral amino acid transporter designated system L (or LAT1), and in fact it does. However, this is not the only system capable of transporting Gln. Indeed, demonstrated that Gln transport into the brain was not inhibited by BCH, a specific inhibitor of LAT1, and did not demonstrate trans-stimulation, suggesting that Gln facilitative transport across the luminal membrane of the BBB occurred by a different system, which was coined system n due to its similarities to system n described in hepatic plasma membrane vesicles.

Nevertheless, other authors point to Systems L (facilitative-transporter) and N (active transport) as having a predominant role in Gln homeostasis, due to abundant expression and endothelium membrane localization of LAT1 and SNAT3 (SCL38A3). In agreement with this hypothesis, the active-transporter system N exporting Gln out of the brain coupled with Na+ was thought to be restricted to the abluminal membrane, but the presence of some members of this system on both sides has been detected in murine and rat models.

Glutamate Transport: Systems XG– and XC–

Studies using isolated membranes from the BBB revealed that facilitative carriers for glutamate (Glu) only existed on the luminal side, while sodium-dependent active co-transporters were confined to the abluminal membrane. Initially, it was tacitly assumed that this Na+-independent transporter was a path for Glu entry into the brain. Several facts contradicted this assumption: (1) Glutamate is a non-essential AA, but it is the most abundant AA in brain, (2) Large doses of Glu within the brain extracellular fluid (physiological range is 0.5–2 mM) induce overexcitation in neurons and thus, this AA is neurotoxic, so its concentration must be tightly controlled, (3) Glu does not enter the brain in appreciable amounts, except in the circumventricular organs and finally, (4) Glu is synthetized in the brain in large quantities. All this evidence indicated that active transporter on the abluminal side triggers the release of Glu from cerebrospinal fluid (CSF) into ECs and, concomitantly, facilitative carriers on the luminal membrane mediate Glu efflux from ECs to plasma.

Regarding the specific facilitative transporters for Glu on the luminal side, there are two plausible candidates. The removal of Glu from ECs to plasma can be mediated by an L-glutamate/L-cystine (Cys2) exchanger, called system XC–. It consists of a catalytic subunit xCT (SLC7A11) that heterodimerizes with a heavy chain 4F2hc (SLC3A2), similarly to LAT1. High mRNA levels of xCT and protein expression are found in border areas of the brain, between the brain and the periphery, such as ECs, choroid plexus, and ependymal cells. System XC– is responsible for Cys2 influx in the luminal membrane of ECs in exchange for internal glutamate; it is a Cys2 transporter that uses the transmembrane gradient of glutamate as the driving force. In agreement with this, it has been demonstrated that uptake of cystine causes glutamate release and that extracellular glutamate inhibits uptake of cystine. Once Cys2 is incorporated into the ECs it is rapidly reduced to Cys, which will either be taken for protein or GSH synthesis within the cells or transported into the CNS through the abluminal membrane by system L.

A second Na+-independent system found in the luminal membrane was described in 1996. Their experiments demonstrated that cysteine did not compete with Glu for uptake, showing that the transport system located at the luminal side was not XC–. Moreover, Asp which is not a substrate for Xc– system, inhibited Glu transport, suggesting that it was XG– the transporter they could detect in their assays. The exact protein that mediates this uptake has yet to be identified.

Both L-glutamate and L-aspartate are “dietary non-essential” AAs, which can be synthesized readily in the brain, so they show much lower rates of uptake into the brain at the BBB; instead brain supply is driven more by intracerebral synthesis and breakdown. Furthermore, reported that the brain uptake for Glu is 5- to 10-fold less than that of most of the large neutral and basic amino acids carried by systems L and y+.

Active Transport Across the BBB

As previously mentioned, the concentration of all naturally occurring AAs in CSF and brain extracellular fluid is 10-20 times lower than in plasma. The only exception is glutamine, whose concentration is similar in CSF and plasma. This gradient on both sides of the BBB is strictly controlled by the different systems of AA transporters. Indeed, AAs leaving the brain toward the circulation are transported against a concentration gradient, so energy is needed. Consequently, active transporters located in the abluminal side of the BBB export AAs from the brain into the endothelial cell, to keep the lower concentration found in the extracellular fluid. These active transporters couple AA exit with Na+ transport. To maintain the sodium gradient required, a Na+-pump is also present at the abluminal membrane of ECs.

Five Na+-dependent systems have been reported in the abluminal side, and more recently some of these systems have also been described on luminal membranes. These systems are: (1) a system for large neutral AA (LNAA); (2) system A (Ala preferring), which was characterized first and transports other small non-essential neutral AAs; (3) system ASC, whose name derived from the main substrates Ala, Ser, and Cys; (4) basic AA transport (Gln, Asn, and His) which is system N; and finally (5) a system for acidic AA, the family of excitatory amino acids transporters (EAATs) that carry preferentially Asp and Glu. (See Table 2 for more details on name, substrates and location of these active transporters) (Figure 2).

These active transporters were thought to be located only in abluminal membranes, and this would reinforce the idea that these carriers remove AAs from the brain benefiting from the Na+-gradient that exists between CSF and ECs. However, more recent publications have shown the presence of Na+-coupled transport at the luminal membranes; this is the case of a carrier from the BAT system (broad substrate amino acid transport) that is B0,+ (or ATB0,+) or even for SNAT3 (a member of system N), that has been located in the mouse capillary luminal and abluminal membranes.

Transport of Large Neutral AAs: System Na+-LNAA

Initially a Na+-dependent transporter for Phe that was inhibited by BCH was described in the BBB. Since system ATB0,+ (SLC6A14) was known as a Na+-dependent transporter that could be inhibited by BCH [2-aminobicyclo-(2,2,1) heptane-2-carboxylic acid], the authors thought that system ATB0,+ was likely to be responsible for Phe transport. However, this hypothesis has never been confirmed, and more recent publications have described the presence of this transporter in the luminal membrane of rat brain slices. ATB0,+ is a plasma membrane transporter, specific for neutral and basic AAs, with the highest affinity for isoleucine and leucine. It transports its substrates in a symport with 2 Na+ and 1 Cl–, coupled to the membrane potential. In vitro experiments with cultured bovine brain capillary ECs showed mRNA levels of this transporter; but other authors could not detect it in freshly isolated BBB mouse endothelial cells, therefore more research is needed. Apart from neutral AAs, ATB0,+ can also transport carnitine, not synthesized in the brain, which is an important precursor of some neurotransmitters.

Another system, also sensitive to BCH inhibition when transporting Phe, has been described on the abluminal side of cow brain capillaries. It is known as system Na+-LNAA (from Na-dependent large neutral amino acids); it has a high-affinity for Leu and is inhibited by other NAAs including Gln, His, Met, Phe, Ser, Thr, and Tyr. The spectrum of substrates is similar to that of system LAT1 that transports essential NAAs with a concentration gradient. It seems that Na+-LNAA in the abluminal membrane removes essential NAAs from the brain, and thus, provides a mechanism for controlling LNAA flux and concentration in CSF. Nevertheless, the molecular identity of system Na+-LNAA remains to be elucidated. According to Nalec KA, a possible candidate could be SBAT1 (SLC6A15), present in the brain and capable of transporting LNAA. Its transport is Na-and pH-dependent, however it does not require Cl– ions. Despite its presence in the brain, little is known about its expression or localization in the BBB. Moreover, the substrate specificities of Na+-LNAA and SBAT1 are not the same, so more research needs to be undertaken to decipher the gene which encodes for this transporter.

Transport of Small Non-essential Neutral AAs: System A

Alanine, serine and cysteine can be transported by the sodium-dependent system A (named A for its preference for Ala as a substrate). This system was found in the abluminal membrane of bovine BBB and it accepts MeAIB [N-(methylamino)isobutyric acid] as a unique substrate, which distinguishes it from other active carriers. It is a voltage-sensitive transporter; three positive charges are translocated per MeAIB molecule. System A mediates the efflux from the brain of small AAs, such as Pro, Gln, Ser, Asn, His, and Ala, helping to maintain the low concentration of these AAs within the CSF. Of the different members of this family, only ATA2 (SLC38A2) has been demonstrated to be expressed in the rat BBB and its expression increases under hypotonic conditions. Indeed, this system accounts for approximately 20% of abluminal Na-dependent Gln transport activity, whereas system N mediates the majority of Gln transport across the abluminal membrane.

Transport of Large and Small Neutral AAs: System ASC

This is a Na+-dependent system located exclusively on the luminal membranes of the BBB, whose name “ASC” was derived from the three main substrates Ala, Ser, and Cys, although Gly and several essential AAs are also putative substrates, including Met, Val, Leu, Iso, and Thr. The presence of this transport system was confirmed by inhibiting system A with MeAIB; ASC activity was not inhibited, and Ala could be transported by this second system. Kinetic studies also revealed that ASC activity is independent of the transmembrane potential.

At least two members of this ASC system have been described in different BBB models. On the one hand, ASCT1 (SLC1A4) was observed in brain ECs during embryonic and neonatal development, but not in adult brains. Furthermore, ASCT2 (SLC1A5) is expressed in higher levels than ASCT1 in the mouse BBB and it was localized at the abluminal side by immunohistochemical analysis.

Transport of Nitrogen-Rich AAs: System N

System N accounts for its preference in AA substrates that are nitrogen-rich, such as His, Gln and Asn, although Ser can also be transported through this system. This transporter exports AAs in a symport with Na+ and antiport with H+ and is voltage-independent. It was first described in the rat BBB at the luminal membrane and it was pH sensitive and moderately tolerant of Li+ substitution for Na+. However, more recently, the presence of SNAT3 (SLC38A3) from the system N amino acid transporter was detected in both sides of the BBB in mouse ECs, while transcripts of SNAT5 (SLC38A5) have also been detected in mouse BBB.

Transport of Acidic AAs: EAATs Transporters

Acidic amino acids Glu and Asp are transported from brain to blood; at the abluminal membrane this efflux is mediated by excitatory amino acid transporters (EAAT), encoded by genes from an SLC1 family. These transporters are voltage-dependent and export Glu and Asp together with 3Na+ and 1H+ in a counter-transport of 1K+ (Nalec 2016). Currently, five members of the EAAT family have been identified in the plasma membranes of astrocytes and neurons as well as in the BBB. Three EAAT members (EAAT1-3) have been detected in the abluminal membrane of the BBB, in different in vivo and in vitro models. cDNAs for these three transporters were isolated from the ECs of cerebral capillaries and experiments with luminal and abluminal membranes demonstrated that they were present exclusively in the abluminal membranes. Regarding other members of this family, a transcript for EAAT4 was detected in brain ECs.

Experiments with specific inhibitors showed that the activity ratio of the three transporters EAAT1: EAAT2: EAAT3 found at the abluminal membrane was 1:3:6, respectively. This family of EAATs is the most powerful of all Na+-dependent transporters of the abluminal side. It was proposed that these transporters play a key role maintaining the glutamate gradient between brain cells and extracellular fluid, since they are the most important players because they catalyze Glu efflux from the brain.

Transport of Taurine Across the BBB

Taurine (2-amino-ethanesulfonic acid) is a sulfur-containing β-amino acid which is quite abundant in the brain. It is synthetized in the liver and enters and leaves the brain through different transporters. Inside the brain it can be an osmoregulator and a neurotransmitter. It has been demonstrated that abluminal membranes had both Na+-dependent taurine transport as well as facilitative transport while luminal membranes only had facilitative transport. However, the system for facilitative transport has yet to be identified.

Regarding the active transport system, presence of the taurine transporter TAUT (SLC6A6) has been shown in rat brain ECs. This transporter is Na+ and Cl–-dependent, it is also voltage-dependent and sensitive to hypertonic conditions. It can be regulated at a transcriptional level by TNFa which also diminishes the efflux of taurine through the BBB in vivo. In 2012, demonstrated in experiments with isolated vesicles from plasma membrane that this active transporter was only located in the abluminal membrane of the BBB. This indicates that taurine can be depleted from the brain even against a concentration gradient across the abluminal membrane.

Concluding Remarks: Organization of the Different Transport Systems

The BBB participates in the control of AA concentrations in the brain, not only for their transport from plasma into the CSF but also for their active removal from the brain through the Na+-dependent transporters located in the abluminal membrane. Systems LAT1 and y+, by being at both sides of the EC plasma membrane, play a central role providing the brain with all essential AAs required. However, there is always more than one transporter capable of moving one specific AA from one side to the other; indeed, there is a substrate overlap among the facilitative systems (Table 1), as well as within the active transporters (Table 2).

The abluminal efflux of AAs from the brain into the ECs and then to the blood takes place against a concentration gradient (∼10-fold higher concentration of AAs in plasma) and thus requires energy. To fulfill this need, there are several Na+-dependent systems located in the abluminal side and a Na+/K+ ATPase that creates the electrochemical gradient of Na+ toward the ECs, allowing the transport of AAs out of the brain. Moreover, these active transporters, located at the abluminal membrane, provide a mechanism for removing essential and non-essential AAs and also other excitatory AAs that can be toxic at higher concentrations. As in the case of facilitative carriers, the majority of AAs can be exported from the brain by more than one transporter, ensuring their removal from the brain and therefore maintaining an optimal concentration within this tissue (Table 2).

The complexity and coupling of all these transport systems relies on the fact that not only ion gradients or voltage gradients regulate transport across the BBB; other molecules might also have a role. This is the case for oxoproline (pyroglutamate), an intermediate molecule of the γ-glutamyl cycle. It has been described that the BBB exhibits a high γ-glutamyl transpeptidase activity and that this enzyme is an integral protein of the luminal membrane of the BBB. A role for γ-glutamyl transpeptidase in AA transport has already been suggested by the group of Meister and others, in several tissues other than the BBB. In fact, intracellular oxoproline stimulates the Na+-dependent systems, especially system A located at the abluminal membrane. This is of particular interest to control the concentration in the brain of small non-essential AAs (which are the main substrates for system A). Thus, the regulation of AA transport by oxoproline may serve to modulate availability of AAs that act as neurotransmitters or their precursors.

Although it has been generally assumed that Na+-dependent transporters were confined to the abluminal membrane, at least two active transporters have been described in the luminal side, ATB0,+ and SNAT3 (system N). ATB0,+ belongs to the broad spectrum of AA transporters and its presence at the luminal side could be explained as a gate-keeper, to ensure AA delivery into the brain under certain pathological conditions. It should also be considered that both systems, ATB0,+ and SNAT3, transport Gln which is the only AA whose concentration is in the same range at both sides of the BBB. Although it is accepted that Gln is transported from the brain to blood, the presence of these transporters at the luminal side could also ensure appropriate levels of this AA when needed.

Finally, it has to be taken into account that some of these AAs are neurotransmitters or precursors and their movement through the BBB is crucial for CNS function. Tyr is a precursor of catecholamines and Trp is a serotonin precursor. These AAs can enter the brain ECs guided by a concentration gradient and there are several systems that allow this entrance (Systems LAT1, Na+-LNAA as well as ATB0,+). On the other hand, some AAs have to be taken out of the brain, which is the case of Glu. An excess of Glu is neurotoxic since it induces hyperexcitation. It has to be removed from the brain extracellular fluid through EAATs transporters (the most powerful of the active transporters) present in astrocytes (EAAT1-3), neurons (EAAT3) and at the abluminal side of the BBB (EAAT1-3) and through systems Xc– and XG– in the luminal membrane. Another AA related to Glu is Gln, which is pumped from brain extracellular fluid into ECs mainly by two active systems, systems A and N (which account for 80% and 20% of Gln release, respectively). Once inside ECs it can also reach circulation by means of facilitative carriers or even be converted into Glu in a reaction catalyzed by glutaminase. In any case, these Glu molecules will traverse the luminal membrane and reach plasma. The BBB restricts the entrance of Glu and Gln; it actively exports these two AAs to the blood instead, protecting the brain from neurotoxicity generated by accumulation of Glu.

Glutamate exerts as an excitatory neurotransmitter by activating a range of neuronal receptors, among them N-methyl-D-aspartate receptors (NMDARs); and these receptors are responsible for many physiological and pathophysiological roles of Glu within the brain. NMDAR have been found in ECs forming the BBB. Indeed, when these receptors are activated by uncontrolled levels of Glu they may disrupt BBB integrity, altering the expression of efflux transporters or reducing the number of tight junctions within the ECs. Moreover, endothelial NMDARs may also affect transport across the BBB in response to Glu levels. These receptors might influence vascular diameter, mediating vasodilation and rising blood flow in brain endothelial cells which in turn increases substrate availability in the BBB.

All in all, the organization of these transporters within the BBB maintains and strictly controls the AA concentrations in brain extracellular fluid. The unequal distribution of those systems between the luminal and abluminal membranes serves to catalyze uptake of specific AAs by the brain and removal of some others. The fact that more than one transporter may carry the same substrate ensures supply and excretion of AAs for proper functioning of the brain and brain homeostasis.

Author Contributions

The author confirms being the sole contributor of this work and has approved it for publication.

Conflict of Interest

The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References 76

  1. 1.

    Abbott N. J. Rönnbäck L. Hansson E. (2006 ). Astrocyte–endothelial interactions at the blood–brain barrier. Nat. Rev. Neurosci. 7 41–53.

    Not in our library10.1038/nrn1824

  2. 2.

    Attwell D. Buchan A. M. Charpak S. Lauritzen M. Macvicar B. A. Newman E. A. (2010 ). Glial and neuronal control of brain blood flow. Nature 468 232–243.

    Not in our library10.1038/nature09613

  3. 3.

    Benrabh H. Lefauconnier J. M. (1996 ). Glutamate is transported across the rat blood-brain barrier by a sodium-independent system. Neurosci. Lett. 210 9–12.

    Not in our library10.1016/0304-3940(96)12635-5

  4. 4.

    Berezowski V. Miecz D. Marszałek M. Broer A. Broer S. Cecchelli R. (2004 ). Involvement of OCTN2 and B0,+ in the transport of carnitine through an in vitro model of the blood-brain barrier. J. Neurochem. 91 860–872.

    Not in our library10.1111/j.1471-4159.2004.02752.x

  5. 5.

    Boado R. J. Li J. Y. Nagaya M. Zhang C. Pardridge W. M. (1999 ). Selective expression of the large neutral amino acid transporter at the blood–brain barrier. Proc. Natl. Acad. Sci. U.S.A. 96 12079–12084.

    Not in our library10.1073/pnas.96.21.12079

  6. 6.

    Brightman M. W. Reese T. S. (1969 ). Junctions between intimately apposed cell membranes in the vertebrate brain. J. Cell Biol. 40 648–677.

    Not in our library10.1083/jcb.40.3.648

  7. 7.

    Burdo J. Dargusch R. Schubert D. (2006 ). Distribution of the cystine/glutamate antiporter system xc- in the brain, kidney, and duodenum. J. Histochem. Cytochem. 54 549–557.

    Not in our library10.1369/jhc.5a6840.2006

  8. 8.

    Carl S. M. Lindley D. J. Couraud P. O. Weksler B. B. Romero I. Mowery S. A. (2010 ). ABC and SLC transporter expression and pot substrate characterization across the human CMEC/D3 blood-brain barrier cell line. Mol. Pharm. 7 1057–1068.

    Not in our library10.1021/mp900178j

  9. 9.

    Cederberg H. H. Uhd N. C. Brodin B. (2014 ). Glutamate efflux at the blood-brain barrier: cellular mechanisms and potential clinical relevance. Arch. Med. Res. 45 639–645.

    Not in our library10.1016/j.arcmed.2014.11.004

  10. 10.

    Cohen-Kashi-Malina K. Cooper I. Teichberg V. I. (2012 ). Mechanisms of glutamate efflux at the blood-brain barrier: involvement of glial cells. J. Cereb. Blood Flow. Metab. 32 177–189.

    Not in our library10.1038/jcbfm.2011.121

  11. 11.

    Coomber B. L. Stewart P. A. (1985 ). Morphometric analysis of CNS microvascular endothelium. Microvasc. Res. 30 99–115.

    Not in our library10.1016/0026-2862(85)90042-1

  12. 12.

    Dahlin A. Royall J. Hohmann J. G. Wang J. (2009 ). Expression profiling of the solute carrier gene family in the mouse brain. J. Pharmacol. Exp. Ther. 329 558–570.

    Not in our library10.1124/jpet.108.149831

  13. 13.

    Daneman R. Prat A. (2015 ). The blood–brain barrier. Cold Spring Harb. Perspect. Biol. 7:a020412.

    Not in our library10.1101/cshperspect.a020412

  14. 14.

    Deves R. Boyd C. A. (1998 ). Transporters for cationic amino acids in animal cells: discovery, structure and function. Physiol. Rev. 78 487–545.

    Not in our library10.1152/physrev.1998.78.2.487

  15. 15.

    Dolgodilina E. Imobersteg S. Laczko E. Welt T. Verrey F. Makrides V. (2016 ). Brain interstitial fluid glutamine homeostasis is controlled by blood-brain barrier SLC7A5/LAT1 amino acid transporter. J. Cereb. Blood Flow. Metab. 36 1929–1941.

    Not in our library10.1177/0271678x15609331

  16. 16.

    Duelli R. Enerson B. E. Gerhart D. Z. Drewes L. R. (2000 ). Expression of large amino acid transporter LAT1 in rat brain endothelium. J. Cereb. Blood Flow. Metab. 20 1557–1562.

    Not in our library10.1097/00004647-200011000-00005

  17. 17.

    Enerson B. E. Drewes L. R. (2006 ). The rat blood-brain barrier transcriptome. J. Cereb. Blood Flow. Metab. 26 959–973.

    Not in our library10.1038/sj.jcbfm.9600249

  18. 18.

    Ennis S. R. Kawai N. Ren X. D. Abdelkarim G. E. Keep R. F. (1998 ). Glutamine uptake at the blood-brain barrier is mediated by N-system transport. J. Neurochem. 71 2565–2573.

    Not in our library10.1046/j.1471-4159.1998.71062565.x

  19. 19.

    Fahlke C. Kortzak D. Machtens J. P. (2016 ). Molecular physiology of EAAT anion channels. Pflugers. Arch. 468 491–502.

    Not in our library10.1007/s00424-015-1768-3

  20. 20.

    Fotiadis D. Kanai Y. Palacín M. (2013 ). The SLC3 and SLC7 families of amino acid transporters. Mol. Aspects Med. 34 139–158.

    Not in our library10.1016/j.mam.2012.10.007.g

  21. 21.

    Geier E. G. Chen E. C. Webb A. Papp A. C. Yee S. W. Sadee W. (2013 ). Profiling solute carrier transporters in the human blood-brain barrier. Clin. Pharmacol. Ther. 94 636–639.

    Not in our library10.1038/clpt.2013.175

  22. 22.

    Gliddon C. M. Shao Z. LeMaistre J. L. Anderson C. M. (2009 ). Cellular distribution of the neutral amino acid transporter subtype ASCT2 in mouse brain. J. Neurochem. 108 372–383.

    Not in our library10.1111/j.1471-4159.2008.05767.x

  23. 23.

    Hall C. N. Reynell C. Gesslein B. Hamilton N. B. Mishra A. Sutherland B. A. (2014 ). Capillary pericytes regulate cerebral blood flow in health and disease. Nature 508 55–60.

    Not in our library10.1038/nature13165

  24. 24.

    Hawkins R. DeJoseph M. R. Hawkins P. A. (1995 ). Regional brain glutamate transport in rats at normal and raised concentrations of circulating glutamate. Cell Tissue Res. 281 207–214.

    Not in our library10.1007/bf00583389

  25. 25.

    Hawkins R. A. O’Kane R. L. Simpson I. A. Viña J. R. (2006 ). Structure of the blood–brain barrier and its role in the transport of amino acids. J. Nutr. 136 218S–226S.

    Not in our library10.1093/jn/136.1.218s

  26. 26.

    Hawkins R. A. Viña J. R. (2016 ). How glutamate is managed by the blood-brain barrier. Biology 5:37.

    Not in our library10.3390/biology5040037

  27. 27.

    Hawkins R. A. Viña J. R. Mokashi A. Peterson D. R. O’Kane R. Simpson I. A. (2013 ). Synergism between the two membranes of the blood-brain barrier: Glucose and amino acid transport. Am. J. Neurosci. Res. 1 1–25.

    Not in our library

  28. 28.

    Hogan-Cann A. D. Anderson C. M. (2016 ). Physiological roles of non-neuronal NMDA receptors. Trends Pharmacol. Sci. 37 750–767.

    Not in our library10.1016/j.tips.2016.05.012

  29. 29.

    Kanai Y. Hediger M. A. (2004 ). The glutamate/neutral amino acid transporter family SLC1: molecular, physiological and pharmacological aspects. Pflugers Arch. 447 469–479.

    Not in our library10.1007/s00424-003-1146-4

  30. 30.

    Kang Y. S. Ohtsuki S. Takanaga H. Tomi M. Hosoya K. Terasaki T. (2002 ). Regulation of taurine transport at the blood-brain barrier by tumor necrosis factor-alpha, taurine, and hypertonicity. J. Neurochem. 83 1188–1195.

    Not in our library10.1046/j.1471-4159.2002.01223.x

  31. 31.

    Lee N. Y. Kang Y. S. (2004 ). The brain-to-blood efflux transport of taurine and changes in the blood-brain barrier transport system by tumor necrosis factor-alpha. Brain Res. 1023 141–147.

    Not in our library10.1016/j.brainres.2004.07.033

  32. 32.

    Lee W. J. Hawkins R. A. Peterson D. R. Viña J. R. (1996 ). Role of oxoproline in the regulation of neutral amino acid transport across the blood-brain barrier. J. Biol. Chem. 271 19129–19133.

    Not in our library10.1074/jbc.271.32.19129

  33. 33.

    Lee W. J. Hawkins R. A. Viña J. R. Peterson D. R. (1998 ). Glutamine transport by the blood-brain barrier: A possible mechanism for nitrogen removal. Am. J. Physiol. 274 C1101–C1107.

    Not in our library10.1152/ajpcell.1998.274.4.c1101

  34. 34.

    Lehre K. P. Levy L. M. Ottersen O. P. Storm-Mathisen J. Danbolt N. C. (1995 ). Differential expression of two glial glutamate transporters in the rat brain: quantitative and immunocytochemical observations. J. Neurosci. 15 1835–1853.

    Not in our library10.1523/jneurosci.15-03-01835.1995

  35. 35.

    Lyck R. Ruderisch N. Moll A. G. Steiner O Cohen C. D. Engelhardt B. (2009 ). Culture-induced changes in blood-brain barrier transcriptome: implications for amino-acid transporters in vivo. J. Cereb. Blood Flow. Metab. 29 1491–1502.

    Not in our library10.1038/jcbfm.2009.72

  36. 36.

    McDonald K. K. Zharikov S. Block E. R. Kilberg M. S. (1997 ). A caveolar complex between the cationic amino acid transporter 1 and endothelial nitric-oxide synthase may explain the “arginine paradox”. J. Biol. Chem. 272 31213–31216.

    Not in our library10.1074/jbc.272.50.31213

  37. 37.

    Meier C. Ristic Z. Klauser S. Verrey F. (2002 ). Activation of system L heterodimeric amino acid exchangers by intracellular substrates. EMBO J. 21 580–589.

    Not in our library10.1093/emboj/21.4.580

  38. 38.

    Michalec K. Mysiorek C. Kuntz M. Berezowski V. Szczepankiewicz A. A. Wilczynski G. M. (2014 ). Protein kinase C restricts transport of carnitine by amino acid transporter ATB(0,+) apically localized in the blood-brain barrier. Arch. Biochem. Biophys. 554 28–35.

    Not in our library10.1016/j.abb.2014.05.006

  39. 39.

    Miralles V. J. Martínez-López I. Zaragozá R. Borrás E. García C. Pallardó F. V. (2001 ). Na+ dependent glutamate transporters (EAAT1, EAAT2, and EAAT3) in primary astrocyte cultures: effect of oxidative stress. Brain Res. 922 21–29.

    Not in our library10.1016/s0006-8993(01)03124-9

  40. 40.

    Nakamura E. Sato M. Yang H. Miyagawa F. Harasaki M. Tomita K. (1999 ). 4F2 (CD98) heavy chain is associated covalently with an amino acid transporter and controls intracellular trafficking and membrane topology of 4F2 heterodimer. J. Biol. Chem. 274 3009–3016.

    Not in our library10.1074/jbc.274.5.3009

  41. 41.

    Nalęcz K. A. (2017 ). Solute carriers in the blood-brain barrier: safety in abundance. Neurochem. Res. 42 795–809.

    Not in our library10.1007/s11064-016-2030-x

  42. 42.

    Napolitano L. Scalise M. Galluccio M. Pochini L. Albanese L. M. Indiveri C. (2015 ). LAT1 is the transport competent unit of the LAT1/CD98 heterodimeric amino acid transporter. Int. J. Biochem. Cell Biol. 67 25–33.

    Not in our library10.1016/j.biocel.2015.08.004

  43. 43.

    Neuwelt E. A. Bauer B. Fahlke C. Fricker G. Iadecola C. Janigro D. (2011 ). Engaging neuroscience to advance translational research in brain barrier biology. Nat. Rev. Neurosci. 12 169–182.

    Not in our library10.1038/nrn2995

  44. 44.

    O’Kane R. L. Hawkins R. A. (2003 ). Na+-dependent transport of large neutral amino acids occurs at the abluminal membrane of the blood-brain barrier. Am. J. Physiol. Endocrinol. Metab. 285 E1167–E1173.

    Not in our library10.1152/ajpendo.00193.2003

  45. 45.

    O’Kane R. L. Martínez-López I. DeJoseph M. R. Viña J. R. Hawkins R. A. (1999 ). Na(+)-dependent glutamate transporters (EAAT1, EAAT2, and EAAT3) of the blood-brain barrier. A mechanism for glutamate removal. J. Biol. Chem. 274 31891–31895.

    Not in our library10.1074/jbc.274.45.31891

  46. 46.

    O’Kane R. L. Viña J. R. Simpson I. Zaragoza R. Mokashi A. Hawkins R. A. (2006 ). Cationic amino acid transport accross the blood-brain barrier is mediated exclusively by System y+. Am. J. Physiol. Endpcrinol. Metab. 291 E412–E419.

    Not in our library10.1152/ajpendo.00007.2006

  47. 47.

    Oldenhorf W. H. Brown W. J. (1975 ). Greater number of capillary endothelial cell mitochondria in brain than in muscle. Proc. Soc. Exp. Biol. Med. 149 736–738.

    Not in our library10.3181/00379727-149-38889

  48. 48.

    Orlowski M. Meister A. (1970 ). The gamma-glutamyl cycle: a possible transport system for amino acids. Proc. Natl. Acad. Sci. U.S.A. 67 1248–1255.

    Not in our library10.1073/pnas.67.3.1248

  49. 49.

    Orlowski M. Sessa G. Green J. P. (1974 ). γ-Glutamyl transpeptidase in brain capillaries: possible site of a blood-brain barrier for amino acids. Science 184 66–68.

    Not in our library10.1126/science.184.4132.66

  50. 50.
  51. 51.

    Peppiatt C. M. Howarth C. Mobbs P. Attwell D. (2006 ). Bidirectional control of CNS capillary diameter by pericytes. Nature 443 700–704.

    Not in our library10.1038/nature05193

  52. 52.

    Rasgado-Flores H. Mokashi A. Hawkins R. A. (2012 ). Na(+)-dependent transport of taurine is found only on the abluminal membrane of the blood-brain barrier. Exp. Neurol. 233 457–462.

    Not in our library10.1016/j.expneurol.2011.11.019

  53. 53.

    Ruderisch N. Virgintino D. Makrides V. Verrey F. (2011 ). Differential axial localization along the mouse brain vascular tree of luminal sodium-dependent glutamine transporters Snat1 and Snat3. J. Cereb. Blood Flow. Metab. 31 1637–1647.

    Not in our library10.1038/jcbfm.2011.21

  54. 54.

    Sakai K. Shimizu H. Koike T. Furuya S. Watanabe M. (2003 ). Neutral amino acid transporter ASCT1 is preferentially expressed in L-Ser-synthetic/storing glial cells in the mouse brain with transient expression in developing capillaries. J. Neurosci. 23 550–560.

    Not in our library10.1523/jneurosci.23-02-00550.2003

  55. 55.

    Sánchez del Pino M. M. Hawkins R. A. Peterson D. R. (1992 ). Neutral amino acid transport by the blood-brain barrier. Membrane vesicle studies. J. Biol. Chem. 267 25951–25957.

    Not in our library

  56. 56.

    Sanchez del Pino M. M. Peterson D. R. Hawkins R. A. (1995 ). Neutral amino acid transport characterization of isolated luminal and abluminal membranes of the blood-brain barrier. J. Biol. Chem. 270 14913–14918.

    Not in our library10.1074/jbc.270.25.14913

  57. 57.

    Sato H. Tamba M. Okuno S. Sato K. Keino-Masu K. Masu M. (2002 ). Distribution of cystine/glutamate exchange transporter, system xc-, in the mouse brain. J. Neurosci. 22 8028–8033.

    Not in our library10.1523/jneurosci.22-18-08028.2002

  58. 58.

    Sims D. E. (1986 ). The pericyte—a review. Tissue Cell 18 153–174.

    Not in our library10.1016/0040-8166(86)90026-1

  59. 59.
  60. 60.

    Skowronska M. Zielinska M. Wojcik-Stanaszek L. Ruszkiewicz J. Milatovic D. Aschner M. (2012 ). Ammonia increases paracellular permeability of rat brain endothelial cells by a mechanism encompassing oxidative/nitrosative stress and activation of matrix metalloproteinases. J. Neurochem. 121 125–134.

    Not in our library10.1111/j.1471-4159.2012.07669.x

  61. 61.

    Smith Q. R. (1991 ). The blood-brain barrier and the regulation of amino acid uptake and availability to brain. Adv. Exp. Med. Biol. 178 414–416.

    Not in our library10.1007/978-1-4684-5931-9_6

  62. 62.

    Smith Q. R. (2000 ). Transport of glutamate and other amino acids at the blood-brain barrier. J. Nutr. 130 1016S–1022S.

    Not in our library10.1093/jn/130.4.1016s

  63. 63.

    Stoll J. Wadhwani K. C. Smith Q. R. (1993 ). Identification of the cationic amino acid transporter (System y+) of the rat blood-brain barrier. J. Neurochem. 60 1956–1959.

    Not in our library10.1111/j.1471-4159.1993.tb13428.x

  64. 64.

    Takanaga H. Mackenzie B. Peng J. B. Hediger M. A. (2005 ). Characterization of a branched-chain amino-acid transporter SBAT1 (SLC6A15) that is expressed in human brain. Biochem. Biophys. Res. Commun. 337 892–900.

    Not in our library10.1016/j.bbrc.2005.09.128

  65. 65.

    Takanaga H. Tokuda N. Ohtsuki S. Hosoya K. Terasaki T. (2002 ). ATA2 is predominantly expressed as system A at the blood-brain barrier and acts as brain-to-blood efflux transport for L-proline. Mol. Pharmacol. 61 1289–1296.

    Not in our library10.1124/mol.61.6.1289

  66. 66.

    Taslimifar M. Buoso S. Verrey F. Kurtcuoglu V. (2018 ). Functional polarity of microvascular brain endothelial cells supported by neurovascular unit computational model of large neutral amino acid homeostasis. Front. Physiol. 9:171.

    Not in our library10.3389/fphys.2018.00171

  67. 67.

    Tayarani I. Lefauconnier J. M. Roux F. Bourre J. M. (1987 ). Evidence for an alanine, serine, and cysteine system of transport in isolated brain capillaries. J. Cereb. Blood Flow. Metab. 7 585–591.

    Not in our library10.1038/jcbfm.1987.109

  68. 68.

    Tetsuka K. Takanaga H. Ohtsuki S. Hosoya K. Terasaki T. (2003 ). The l-isomer-selective transport of aspartic acid is mediated by ASCT2 at the blood-brain barrier. J. Neurochem. 87 891–901.

    Not in our library10.1046/j.1471-4159.200302063.x

  69. 69.

    Tewes B. J. Galla H. J. (2001 ). Lipid polarity in brain capillary endothelial cells. Endothelium 8 207–220.

    Not in our library10.1080/10623320109051566

  70. 70.

    Valdovinos-Flores C. Gonsebatt M. E. (2012 ). The role of amino acid transporters in GSH synthesis in the blood-brain barrier and central nervous system. Neurochem. Int. 61 405–414.

    Not in our library10.1016/j.neuint.2012.05.019

  71. 71.

    Van Meer G. Simons K. (1986 ). The function of tight junctions in maintaining differences in lipid composition between the apical and the basolateral cell surface domains of mdck cells. EMBO J. 5 1455–1464.

    Not in our library10.1002/j.1460-2075.1986.tb04382.x

  72. 72.

    Viña J. Puertes I. R. Estrela J. M. Viña J. R. Galbis J. L. (1981 ). Involvement of gamma-glutamyltransferase in amino-acid uptake by the lactating mammary gland of the rat. Biochem J. 194 99–102.

    Not in our library10.1042/bj1940099

  73. 73.

    Viña J. R. Blay P. Ramirez A. Castells A. Viña J. (1990 ). Inhibition of gamma-glutamyl transpeptidase decreases amino acid uptake in human keratinocytes in culture. FEBS Lett. 269 86–88.

    Not in our library10.1016/0014-5793(90)81125-8

  74. 74.

    Viña J. R. Palacin M. Puertes I. R. Hernandez R. Viña J. (1989 ). Role of the gamma-glutamyl cycle in the regulation of amino acid translocation. Am. J. Physiol. 257 E916–E922.

    Not in our library10.1152/ajpendo.1989.257.6.e916

  75. 75.
  76. 76.

    Zlokovic B. V. (2008 ). The blood–brain barrier in health and chronic neurodegenerative disorders. Neuron 57 178–201.

    Not in our library10.1016/j.neuron.2008.01.003

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