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Role of PGC‐1α signaling in skeletal muscle health and disease
Chounghun Kang, Li Li Ji
Annals of the New York Academy of Sciences · 2012 · Review
doi:10.1111/j.1749-6632.2012.06738.x
Abstract
This paper reviews the current understanding of the molecular basis of the peroxisome proliferator‐activated receptor‐γ coactivator‐1α (PGC‐1α)–mediated pathway and discusses the role of PGC‐1α in skeletal muscle atrophy caused by immobilization. PGC‐1α is the master transcription regulator that stimulates mitochondrial biogenesis, by upregulating nuclear respiratory factors (NRF‐1, 2) and mitochondrial transcription factor A (Tfam), which leads to increased mitochondrial DNA replication and gene transcription. PGC‐1α also regulates cellular oxidant–antioxidant homeostasis by stimulating the gene expression of superoxide dismutase‐2 (SOD2), catalase, glutathione peroxidase 1 (GPx1), and uncoupling protein (UCP). Recent reports from muscle‐specific PGC‐1α overexpression underline the importance of PGC‐1α in atrophied skeletal muscle, demonstrate enhancement of the PGC‐1α mitochondrial biogenic pathway, and reduced oxidative damage. Thus, PGC‐1α appears to play a protective role against atrophy‐linked skeletal muscle deterioration.
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References 63
- 1.
Hoppeler H, Fluck M. Plasticity of skeletal muscle mitochondria: structure and function. Med. Sci. Sports Exer. 2003;35:95-104.
Not in our library10.1249/01.mss.0000043292.99104.12
- 2.
Handschin C, Spiegelman BM. The role of exercise and PGC1α in inflammation and chronic disease. Nature. 2008;454:463-469.
Not in our library10.1038/nature07206
- 3.
Puigserver P, Wu Z, Park CW, et al. A cold-inducible coactivator of nuclear receptors linked to adaptive thermogenesis. Cell. 1998;92:829-839.
Not in our library10.1016/s0092-8674(00)81410-5
- 4.
Lin J, Wu H, Tarr PT. Transcriptional co-activator PGC-1α drives the formation of slow-twitch muscle fibres. Nature. 2002;418:797-801.
Not in our library10.1038/nature00904
- 5.
Wu Z, Puigserver P, Andersson U, et al. Mechanisms controlling mitochondrial biogenesis and function through the thermogeniccoactivator PGC-1. Cell. 1999;98:115-124.
Not in our library10.1016/s0092-8674(00)80611-x
- 6.
Finck BN, Kelly DP. PGC-1 coactivators: inducible regulators of energy metabolism in health and disease. J. Clin. Invest. 2006;116:615-622.
Not in our library10.1172/jci27794
- 7.
Puigserver P, Spiegelman BM. Peroxisome proliferators-activated receptor gamma coactivator 1α (PGC-1α): transcriptional coactivator and metabolic regulator. Endocr. Rev. 2003;24:78-90.
Not in our library10.1210/er.2002-0012
- 8.
Mootha VK, et al. PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes. Nature Genet. 2003;34:267-273.
Not in our library10.1038/ng1180
- 9.
Scarpulla RC. Transcriptional paradigms in mammalian mitochondrial biogenesis and function. Physiol. Rev. 2008;88:611-638.
Not in our library10.1152/physrev.00025.2007
- 10.
Knutti D, Kralli A. PGC-1, a versatile coactivator. Trends Endocrinol. Metab. 2001;12:360-365.
Not in our library10.1016/s1043-2760(01)00457-x
- 11.
Russell AP. PGC-1α and exercise: important partners in combating insulin resistance. Curr. Diabetes Rev. 2005;1:175-184.
Not in our library10.2174/1573399054022811
- 12.
Kelly DP, Scarpulla RC. Transcriptional regulatory circuits controlling mitochondrial biogenesis and function. Genes Dev. 2007;18:357-368.
Not in our library10.1101/gad.1177604
- 13.
Lin J, Handschin C, Spiegelman BM. Metabolic control through the PGC-1 family of transcription coactivators. Cell Metabol. 2005;1:361-370.
Not in our library10.1016/j.cmet.2005.05.004
- 14.
Wu Z, Puigserver P, Andersson U, et al. Mechanisms controlling mitochondrial biogenesis and respiration through the thermogeniccoactivator PGC-1. Cell. 1999;98:115-124.
Not in our library10.1016/s0092-8674(00)80611-x
- 15.
Lin J, Wu H, Tarr PT. Transcriptional co-activator PGC-1α drives the formation of slow-twitch muscle fibres. Nature. 2002;418:797-801.
Not in our library10.1038/nature00904
- 16.
Michael LF, Wu Z, Cheatham RB. Restoration of insulin-sensitive glucose transporter (GLUT4) gene expression in muscle cells by the transcriptional coactivator PGC-1. Proc. Natl. Acad. Sci. USA. 2001;98:3820-3825.
Not in our library10.1073/pnas.061035098
- 17.
Jagoe RT, Goldberg AL. What do we really know about the ubiquitin—proteasome pathway in muscle atrophy? Curr. Opin. Clin. Nutr. Metab. Care. 2001;4:183-190.
Not in our library10.1097/00075197-200105000-00003
- 18.
Schreiber SN, Emter R, Hock MB. The estrogen-related receptor a (ERRα) functions in PPARccoactivator 1a (PGC-1α)-induced mitochondrial biogenesis. Proc. Natl. Acad. Sci. USA. 2004;101:6472-6477.
Not in our library10.1073/pnas.0308686101
- 19.
Russell LK, Mansfield CM, Lehman JJ, et al. Cardiac-specific induction of the transcriptional coactivator peroxisome proliferator-activated receptor γ coactivator-1α promotes mitochondrial biogenesis and reversible cardiomyopathy in a developmental stagre-dependent manner. Circ. Res. 2004;94:525-533.
Not in our library10.1161/01.res.0000117088.36577.eb
- 20.
Lehman JJ, Barger PM, Kovacs A, et al. Peroxisome proliferator-activated receptor γ coactivator-1 promotes cardiac mitochondrial biogenesis. J. Clin. Invest. 2000;106:847-856.
Not in our library10.1172/jci10268
- 21.
Lindholm D, Eriksson O, Mäkelä J, et al. PGC-1a: a master gene that is hard to master. Cell Mol. Life Sci. 2012;69:2465-2468.
Not in our library10.1007/s00018-012-1043-0
- 22.
Wareski P, Vaarmann A, Choubey V, et al. PGC-1α and PGC-1β regulate mitochondrial density in neurons. J. Biol. Chem. 2009;284:21379-21385.
Not in our library10.1074/jbc.m109.018911
- 23.
Leick L, Wojtaszewsk IJF, Johansen ST. PGC-1α is not mandatory for exercise- and training-induced adaptive gene responses in mouse skeletal muscle. Am. J. Physiol. 2008;294:E463-E474.
Not in our library10.1152/ajpendo.00666.2007
- 24.
Geng T, Li P, Okutsu M. PGC-1α plays a functional role in exercise-induced mitochondrial biogenesis and angiogenesis but not fiber-type transformation in mouse skeletal muscle. Am. J. Physiol. Cell Physiol. 2010;298:572-579.
Not in our library10.1152/ajpcell.00481.2009
- 25.
Leick L, Lyngby SS, Wojtasewski JF, Pilegaard H. PGC-1α is required for training-induced prevention of age-associated decline in mitochondrial enzymes in mouse skeletal muscle. Exp. Gerontol. 2010;45:336-342.
Not in our library10.1016/j.exger.2010.01.011
- 26.
Wenz T, Rossi S, Rotundo RL. Increased muscle PGC-1α expression protects from sarcopenia and metabolic disease during aging. PNAS. 2009;106:20405-20410.
Not in our library10.1073/pnas.0911570106
- 27.
St-Pierre J, Drori S, Uldry M. Suppression of reactive oxygen species and neurodegeneration by the PGC-1 transcriptional coactivators. Cell. 2006;127:397-408.
Not in our library10.1016/j.cell.2006.09.024
- 28.
St-Pierre J, Lin J, Krauss S. Bioenergetic analysis of peroxisome proliferator-activated receptor gamma coactivators 1alpha and 1beta (PGC-1alpha and PGC-1beta) in muscle cells. J. Biol. Chem. 2003;278:26597-26603.
Not in our library10.1074/jbc.m301850200
- 29.
- 30.
Shi T, Wang F, Stieren E, Tong Q. SIRT3, a mitochondrial sirtuindeacetylase, regulates mitochondrial function and thermogenesis in brown adipocytes. J. Biol. Chem. 2005;280:13560e13567.
Not in our library10.1074/jbc.m414670200
- 31.
Bellizzi D, et al. A novel VNTR enhancer within the SIRT3 gene, a human homologue of SIR2, is associated with survival at oldest ages. Genomics. 2005;85:258e263.
Not in our library10.1016/j.ygeno.2004.11.003
- 32.
Arnold AS, Egger A, Handschin C. PGC-1α and myokines in the aging muscle—a mini-review. Gerontology. 2010;57:37-43.
Not in our library10.1159/000281883
- 33.
Handschin C. Peroxisome proliferator-activated receptor-γ coactivator-1α in muscle links metabolism to inflammation. Clin. Exp. Pharmacol. Physiol. 2009;36:1139-1143.
Not in our library10.1111/j.1440-1681.2009.05275.x
- 34.
Van der Heiden K, Cuhlmann S, Luong leA, et al. Role of nuclear factor kappaB in cardiovascular health and disease. Clin. Sci. 2010;118:593-605.
Not in our library10.1042/cs20090557
- 35.
Baldwin AS. The NF-kappa B and I kappa B proteins: new discoveries and insights. Annu. Rev. Immunol. 1996;14:649-683.
Not in our library10.1146/annurev.immunol.14.1.649
- 36.
Ji LL. Modulation of skeletal muscle antioxidant defense by exercise: role of redox signaling. Free Radic. Biol. Med. 2008;44:142-152.
Not in our library10.1016/j.freeradbiomed.2007.02.031
- 37.
Valle I, et al. PGC-1α regulates the mitochondrial antioxidant defense system in vascular endothelial cells. Cardiovasc. Res. 2005;66:562-573.
Not in our library10.1016/j.cardiores.2005.01.026
- 38.
Handschin C, Chin S, Li P, et al. Skeletal muscle fiber-type switching, exercise intolerance, and myopathy in PGC-1α muscle-specific knock-out animals. J. Biol. Chem. 2007;282:30014-30021.
Not in our library10.1074/jbc.m704817200
- 39.
Wellen KE, Hotamisligil GS. Inflammation, stress, and diabetes. J. Clin. Invest. 2005;115:1111-1119.
Not in our library10.1172/jci25102
- 40.
Holloszy JO. Biochemical adaptations in muscle. Effects of exercise on mitochondrial oxygen uptake and respiratory enzyme activity in skeletal muscle. J. Biol. Chem. 1967;242:2278-2282.
Not in our library
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