User menu

Accès à distance ? S'identifier sur le proxy UCLouvain

Myostatin and the skeletal muscle atrophy and hypertrophy signaling pathways.

  1. Rüegg Markus A., Glass David J., Molecular Mechanisms and Treatment Options for Muscle Wasting Diseases, 10.1146/annurev-pharmtox-010510-100537
  2. Glass David J., Skeletal muscle hypertrophy and atrophy signaling pathways, 10.1016/j.biocel.2005.04.018
  3. Sandri Marco, Signaling in Muscle Atrophy and Hypertrophy, 10.1152/physiol.00041.2007
  4. Elliott B., Renshaw D., Getting S., Mackenzie R., The central role of myostatin in skeletal muscle and whole body homeostasis, 10.1111/j.1748-1716.2012.02423.x
  5. McPherron Alexandra C., Lawler Ann M., Lee Se-Jin, Regulation of skeletal muscle mass in mice by a new TGF-p superfamily member, 10.1038/387083a0
  6. Mosher Dana S., Quignon Pascale, Bustamante Carlos D., Sutter Nathan B., Mellersh Cathryn S., Parker Heidi G., Ostrander Elaine A., A Mutation in the Myostatin Gene Increases Muscle Mass and Enhances Racing Performance in Heterozygote Dogs, 10.1371/journal.pgen.0030079
  7. Grobet Luc, Royo Martin Luis José, Poncelet Dominique, Pirottin Dimitri, Brouwers Benoit, Riquet Juliette, Schoeberlein Andreina, Dunner Susana, Ménissier François, Massabanda Julio, Fries Ruedi, Hanset Roger, Georges Michel, A deletion in the bovine myostatin gene causes the double–muscled phenotype in cattle, 10.1038/ng0997-71
  8. Kambadur R, Sharma M, Smith TP, Bass JJ (1997) Mutations in myostatin (GDF8) in double-muscled Belgian Blue and Piedmontese cattle. Genome Res 7(9):910–916
  9. Clop Alex, Marcq Fabienne, Takeda Haruko, Pirottin Dimitri, Tordoir Xavier, Bibé Bernard, Bouix Jacques, Caiment Florian, Elsen Jean-Michel, Eychenne Francis, Larzul Catherine, Laville Elisabeth, Meish Françoise, Milenkovic Dragan, Tobin James, Charlier Carole, Georges Michel, A mutation creating a potential illegitimate microRNA target site in the myostatin gene affects muscularity in sheep, 10.1038/ng1810
  10. Schuelke Markus, Wagner Kathryn R., Stolz Leslie E., Hübner Christoph, Riebel Thomas, Kömen Wolfgang, Braun Thomas, Tobin James F., Lee Se-Jin, Myostatin Mutation Associated with Gross Muscle Hypertrophy in a Child, 10.1056/nejmoa040933
  11. Szabó Gyula, Dallmann Géza, Müller Géza, Patthy László, Soller Morris, Varga László, A deletion in the myostatin gene causes the compact ( Cmpt ) hypermuscular mutation in mice, 10.1007/s003359900843
  12. Grobet Luc, Pirottin Dimitri, Farnir Fr�d�ric, Poncelet Dominique, Royo Luis Jose, Brouwers Beno�t, Christians Elisabeth, Desmecht Daniel, Coignoul Freddy, Kahn Ronald, Georges Michel, Modulating skeletal muscle mass by postnatal, muscle-specific inactivation of the myostatin gene, 10.1002/gene.10188
  13. Whittemore Lisa-Anne, Song Kening, Li Xiangping, Aghajanian Jane, Davies Monique, Girgenrath Stefan, Hill Jennifer J., Jalenak Mary, Kelley Pamela, Knight Andrea, Maylor Rich, O’Hara Denise, Pearson Adele, Quazi Amira, Ryerson Stephanie, Tan Xiang-Yang, Tomkinson Kathleen N., Veldman Geertruida M., Widom Angela, Wright Jill F., Wudyka Steve, Zhao Liz, Wolfman Neil M., Inhibition of myostatin in adult mice increases skeletal muscle mass and strength, 10.1016/s0006-291x(02)02953-4
  14. Rebbapragada A., Benchabane H., Wrana J. L., Celeste A. J., Attisano L., Myostatin Signals through a Transforming Growth Factor  -Like Signaling Pathway To Block Adipogenesis, 10.1128/mcb.23.20.7230-7242.2003
  15. Lee S.-J., McPherron A. C., Regulation of myostatin activity and muscle growth, 10.1073/pnas.151270098
  16. Derynck Rik, Zhang Ying, Feng Xin-Hua, Transcriptional Activators of TGF-β Responses: Smads, 10.1016/s0092-8674(00)81696-7
  17. Forbes Davanea, Jackman Mark, Bishop Amy, Thomas Mark, Kambadur Ravi, Sharma Mridula, Myostatin auto-regulates its expression by feedback loop through Smad7 dependent mechanism : AUTO-REGULATION OF MYOSTATIN, 10.1002/jcp.20477
  18. Zhu Xiangyang, Topouzis Stavros, Liang Li-fang, Stotish Ronald L., Myostatin signaling through Smad2, Smad3 and Smad4 is regulated by the inhibitory Smad7 by a negative feedback mechanism, 10.1016/j.cyto.2004.03.007
  19. Sartori Roberta, Milan Giulia, Patron Maria, Mammucari Cristina, Blaauw Bert, Abraham Reimar, Sandri Marco, Smad2 and 3 transcription factors control muscle mass in adulthood, 10.1152/ajpcell.00104.2009
  20. Trendelenburg Anne Ulrike, Meyer Angelika, Rohner Daisy, Boyle Joseph, Hatakeyama Shinji, Glass David J., Myostatin reduces Akt/TORC1/p70S6K signaling, inhibiting myoblast differentiation and myotube size, 10.1152/ajpcell.00105.2009
  21. Sartori Roberta, Schirwis Elija, Blaauw Bert, Bortolanza Sergia, Zhao Jinghui, Enzo Elena, Stantzou Amalia, Mouisel Etienne, Toniolo Luana, Ferry Arnaud, Stricker Sigmar, Goldberg Alfred L, Dupont Sirio, Piccolo Stefano, Amthor Helge, Sandri Marco, BMP signaling controls muscle mass, 10.1038/ng.2772
  22. Liu Wei, Thomas Scott G., Asa Sylvia L., Gonzalez-Cadavid Nestor, Bhasin Shalendar, Ezzat Shereen, Myostatin Is a Skeletal Muscle Target of Growth Hormone Anabolic Action, 10.1210/jc.2003-030497
  23. Brill Kimberly T., Weltman Arthur L., Gentili Angela, Patrie James T., Fryburg David A., Hanks John B., Urban Randall J., Veldhuis Johannes D., Single and Combined Effects of Growth Hormone and Testosterone Administration on Measures of Body Composition, Physical Performance, Mood, Sexual Function, Bone Turnover, and Muscle Gene Expression in Healthy Older Men, 10.1210/jc.2002-020098
  24. Mendler Luca, Baka Zsuzsanna, Kovács-Simon Andrea, Dux László, Androgens negatively regulate myostatin expression in an androgen-dependent skeletal muscle, 10.1016/j.bbrc.2007.07.023
  25. Braga Melissa, Bhasin Shalender, Jasuja Ravi, Pervin Shehla, Singh Rajan, Testosterone inhibits transforming growth factor-β signaling during myogenic differentiation and proliferation of mouse satellite cells: Potential role of follistatin in mediating testosterone action, 10.1016/j.mce.2011.11.019
  26. Dubois V, Laurent MR, Sinnesael M, Cielen N, Helsen C, Clinckemalie L, Spans L, Gayan-Ramirez G, Deldicque L, Hespel P, Carmeliet G, Vanderschueren D, Claessens F (2014) A satellite cell-specific knockout of the androgen receptor reveals myostatin as a direct androgen target in skeletal muscle. FASEB J. doi: 10.1096/fj.14-249748
  27. Kim Jeong-su, Cross James M., Bamman Marcas M., Impact of resistance loading on myostatin expression and cell cycle regulation in young and older men and women, 10.1152/ajpendo.00464.2004
  28. Michel Robin N., Dunn Shannon E., Chin Eva R., Calcineurin and skeletal muscle growth, 10.1079/pns2004362
  29. Ruas Jorge L., White James P., Rao Rajesh R., Kleiner Sandra, Brannan Kevin T., Harrison Brooke C., Greene Nicholas P., Wu Jun, Estall Jennifer L., Irving Brian A., Lanza Ian R., Rasbach Kyle A., Okutsu Mitsuharu, Nair K. Sreekumaran, Yan Zhen, Leinwand Leslie A., Spiegelman Bruce M., A PGC-1α Isoform Induced by Resistance Training Regulates Skeletal Muscle Hypertrophy, 10.1016/j.cell.2012.10.050
  30. Roth SM, Martel GF, Ferrell RE, Metter EJ, Hurley BF, Rogers MA (2003) Myostatin gene expression is reduced in humans with heavy-resistance strength training: a brief communication. Exp Biol Med (Maywood) 228(6):706–709
  31. Willoughby Darryn S., Effects of an Alleged Myostatin-Binding Supplement and Heavy Resistance Training on Serum Myostatin, Muscle Strength and Mass, and Body Composition, 10.1123/ijsnem.14.4.461
  32. WILLOUGHBY DARRYN S., Effects of Heavy Resistance Training on Myostatin mRNA and Protein Expression : , 10.1249/01.mss.0000121952.71533.ea
  33. Hayot Maurice, Rodriguez Julie, Vernus Barbara, Carnac Gilles, Jean Elise, Allen David, Goret Lucie, Obert Philippe, Candau Robin, Bonnieu Anne, Myostatin up-regulation is associated with the skeletal muscle response to hypoxic stimuli, 10.1016/j.mce.2010.09.008
  34. Yarasheski KE, Bhasin S, Sinha-Hikim I, Pak-Loduca J, Gonzalez-Cadavid NF (2002) Serum myostatin-immunoreactive protein is increased in 60–92 year old women and men with muscle wasting. J Nutr Health Aging 6(5):343–348
  35. Ratkevicius A., Joyson A., Selmer I., Dhanani T., Grierson C., Tommasi A. M., DeVries A., Rauchhaus P., Crowther D., Alesci S., Yaworsky P., Gilbert F., Redpath T. W., Brady J., Fearon K. C. H., Reid D. M., Greig C. A., Wackerhage H., Serum Concentrations of Myostatin and Myostatin-Interacting Proteins Do Not Differ Between Young and Sarcopenic Elderly Men, 10.1093/gerona/glr025
  36. Siriett Victoria, Platt Leanne, Salerno Mônica Senna, Ling Nicholas, Kambadur Ravi, Sharma Mridula, Prolonged absence of myostatin reduces sarcopenia, 10.1002/jcp.20778
  37. Murphy Kate T., Koopman René, Naim Timur, Léger Bertrand, Trieu Jennifer, Ibebunjo Chikwendu, Lynch Gordon S., Antibody-directed myostatin inhibition in 21-mo-old mice reveals novel roles for myostatin signaling in skeletal muscle structure and function, 10.1096/fj.10-159608
  38. Kawada Shigeo, Tachi Chikashi, Ishii Naokata, 10.1023/a:1016366409691
  39. Baumann AP, Ibebunjo C, Grasser WA, Paralkar VM (2003) Myostatin expression in age and denervation-induced skeletal muscle atrophy. J Musculoskelet Neuronal Interact 3(1):8–16
  40. Carlson CJ, Booth FW, Gordon SE (1999) Skeletal muscle myostatin mRNA expression is fiber-type specific and increases during hindlimb unloading. Am J Physiol 277(2 Pt 2):R601–R606
  41. Oldham Jenny M., Osepchook Claire C., Jeanplong Ferenc, Falconer Shelley J., Matthews Kenneth G., Conaglen John V., Gerrard David F., Smith Heather K., Wilkins Richard J., Bass James J., McMahon Christopher D., The decrease in mature myostatin protein in male skeletal muscle is developmentally regulated by growth hormone : GH regulates the post-translational decrease in myostatin, 10.1113/jphysiol.2008.161521
  42. Ohsawa Yutaka, Hagiwara Hiroki, Nakatani Masashi, Yasue Akihiro, Moriyama Keiji, Murakami Tatsufumi, Tsuchida Kunihiro, Noji Sumihare, Sunada Yoshihide, Muscular atrophy of caveolin-3–deficient mice is rescued by myostatin inhibition, 10.1172/jci28520
  43. Gilson H., Schakman O., Combaret L., Lause P., Grobet L., Attaix D., Ketelslegers J. M., Thissen J. P., Myostatin Gene Deletion Prevents Glucocorticoid-Induced Muscle Atrophy, 10.1210/en.2006-0539
  44. Salehian Behrouz, Mahabadi Vahid, Bilas Josephine, Taylor Wayne E., Ma Kun, The effect of glutamine on prevention of glucocorticoid-induced skeletal muscle atrophy is associated with myostatin suppression, 10.1016/j.metabol.2006.05.009
  45. Zimmers T. A., Induction of Cachexia in Mice by Systemically Administered Myostatin, 10.1126/science.1069525
  46. Durieux Anne-Cécile, Amirouche Adel, Banzet Sébastien, Koulmann Nathalie, Bonnefoy Régis, Pasdeloup Marielle, Mouret Catherine, Bigard Xavier, Peinnequin André, Freyssenet Damien, Ectopic Expression of Myostatin Induces Atrophy of Adult Skeletal Muscle by Decreasing Muscle Gene Expression, 10.1210/en.2006-1500
  47. Amirouche Adel, Durieux Anne-Cécile, Banzet Sébastien, Koulmann Nathalie, Bonnefoy Régis, Mouret Catherine, Bigard Xavier, Peinnequin André, Freyssenet Damien, Down-Regulation of Akt/Mammalian Target of Rapamycin Signaling Pathway in Response to Myostatin Overexpression in Skeletal Muscle, 10.1210/en.2008-0959
  48. McMahon Christopher D., Popovic Ljiljana, Oldham Jenny M., Jeanplong Ferenc, Smith Heather K., Kambadur Ravi, Sharma Mridula, Maxwell Linda, Bass James J., Myostatin-deficient mice lose more skeletal muscle mass than wild-type controls during hindlimb suspension, 10.1152/ajpendo.00275.2002
  49. Bischoff Richard, Heintz Catherine, Enhancement of skeletal muscle regeneration, 10.1002/aja.1002010105
  50. Schmalbruch H, al-Amood W S, Lewis D M, Morphology of long-term denervated rat soleus muscle and the effect of chronic electrical stimulation., 10.1113/jphysiol.1991.sp018748
  51. Cooper RN, Tajbakhsh S, Mouly V, Cossu G, Buckingham M, Butler-Browne GS (1999) In vivo satellite cell activation via Myf5 and MyoD in regenerating mouse skeletal muscle. J Cell Sci 112(Pt 17):2895–2901
  52. McCroskery Seumas, Thomas Mark, Maxwell Linda, Sharma Mridula, Kambadur Ravi, Myostatin negatively regulates satellite cell activation and self-renewal, 10.1083/jcb.200207056
  53. Magee Thomas R., Artaza Jorge N., Ferrini Monica G., Vernet Dolores, Zuniga Freddi I., Cantini Liliana, Reisz-Porszasz Suzanne, Rajfer Jacob, Gonzalez-Cadavid Nestor F., Myostatin short interfering hairpin RNA gene transfer increases skeletal muscle mass, 10.1002/jgm.946
  54. Amthor H., Otto A., Vulin A., Rochat A., Dumonceaux J., Garcia L., Mouisel E., Hourde C., Macharia R., Friedrichs M., Relaix F., Zammit P. S., Matsakas A., Patel K., Partridge T., Muscle hypertrophy driven by myostatin blockade does not require stem/precursor-cell activity, 10.1073/pnas.0811129106
  55. Welle Stephen, Mehta Sangeeta, Burgess Kerri, Effect of postdevelopmental myostatin depletion on myofibrillar protein metabolism, 10.1152/ajpendo.00509.2010
  56. Lee S.-J., Huynh T. V., Lee Y.-S., Sebald S. M., Wilcox-Adelman S. A., Iwamori N., Lepper C., Matzuk M. M., Fan C.-M., Role of satellite cells versus myofibers in muscle hypertrophy induced by inhibition of the myostatin/activin signaling pathway, 10.1073/pnas.1206410109
  57. Rodriguez Julie, Vernus Barbara, Toubiana Mylène, Jublanc Elodie, Tintignac Lionel, Leibovitch Serge, Bonnieu Anne, Myostatin inactivation increases myotube size through regulation of translational initiation machinery, 10.1002/jcb.23280
  58. Wang Qian, McPherron Alexandra C., Myostatin inhibition induces muscle fibre hypertrophy prior to satellite cell activation, 10.1113/jphysiol.2011.226001
  59. Thomas Mark, Langley Brett, Berry Carole, Sharma Mridula, Kirk Sonnie, Bass John, Kambadur Ravi, Myostatin, a Negative Regulator of Muscle Growth, Functions by Inhibiting Myoblast Proliferation, 10.1074/jbc.m004356200
  60. Rı́os Ramón, Carneiro Isabel, Arce Víctor M., Devesa Jesús, Myostatin is an inhibitor of myogenic differentiation, 10.1152/ajpcell.00372.2001
  61. Taylor WE, Bhasin S, Artaza J, Byhower F, Azam M, Willard DH Jr, Kull FC Jr, Gonzalez-Cadavid N (2001) Myostatin inhibits cell proliferation and protein synthesis in C2C12 muscle cells. Am J Physiol Endocrinol Metab 280(2):E221–E228
  62. Joulia Dominique, Bernardi Henri, Garandel Véronique, Rabenoelina Fanjaniriana, Vernus Barbara, Cabello Gérard, Mechanisms involved in the inhibition of myoblast proliferation and differentiation by myostatin, 10.1016/s0014-4827(03)00074-0
  63. Yang W., Zhang Y., Li Y., Wu Z., Zhu D., Myostatin Induces Cyclin D1 Degradation to Cause Cell Cycle Arrest through a Phosphatidylinositol 3-Kinase/AKT/GSK-3beta Pathway and Is Antagonized by Insulin-like Growth Factor 1, 10.1074/jbc.m610185200
  64. Langley Brett, Thomas Mark, Bishop Amy, Sharma Mridula, Gilmour Stewart, Kambadur Ravi, Myostatin Inhibits Myoblast Differentiation by Down-regulating MyoD Expression, 10.1074/jbc.m204291200
  65. McFarlane Craig, Hui Gu Zi, Amanda Wong Zhi Wei, Lau Hiu Yeung, Lokireddy Sudarsanareddy, XiaoJia Ge, Mouly Vincent, Butler-Browne Gillian, Gluckman Peter D., Sharma Mridula, Kambadur Ravi, Human myostatin negatively regulates human myoblast growth and differentiation, 10.1152/ajpcell.00012.2011
  66. Amthor Helge, Huang Ruijin, McKinnell Iain, Christ Bodo, Kambadur Ravi, Sharma Mridula, Patel Ketan, The Regulation and Action of Myostatin as a Negative Regulator of Muscle Development during Avian Embryogenesis, 10.1006/dbio.2002.0812
  67. Salerno Mônica Senna, Thomas Mark, Forbes Davanea, Watson Trevor, Kambadur Ravi, Sharma Mridula, Molecular analysis of fiber type-specific expression of murine myostatin promoter, 10.1152/ajpcell.00492.2003
  68. Yang Wei, Chen Yan, Zhang Yong, Wang Xueyan, Yang Ning, Zhu Dahai, Extracellular Signal–Regulated Kinase 1/2 Mitogen-Activated Protein Kinase Pathway Is Involved in Myostatin-Regulated Differentiation Repression, 10.1158/0008-5472.can-05-3060
  69. Chelh Ilham, Meunier Bruno, Picard Brigitte, Reecy Mark, Chevalier Catherine, Hocquette Jean-François, Cassar-Malek Isabelle, Molecular profiles of Quadriceps muscle in myostatin-null mice reveal PI3K and apoptotic pathways as myostatin targets, 10.1186/1471-2164-10-196
  70. Chelh I., Picard B., Hocquette J-F., Cassar-Malek I., Myostatin inactivation induces a similar muscle molecular signature in double-muscled cattle as in mice, 10.1017/s1751731110001862
  71. Rommel Christian, Bodine Sue C., Clarke Brian A., Rossman Roni, Nunez Lorna, Stitt Trevor N., Yancopoulos George D., Glass David J., Mediation of IGF-1-induced skeletal myotube hypertrophy by PI(3)K/Akt/mTOR and PI(3)K/Akt/GSK3 pathways, 10.1038/ncb1101-1009
  72. Bodine Sue C., Stitt Trevor N., Gonzalez Michael, Kline William O., Stover Gretchen L., Bauerlein Roy, Zlotchenko Elizabeth, Scrimgeour Angus, Lawrence John C., Glass David J., Yancopoulos George D., Akt/mTOR pathway is a crucial regulator of skeletal muscle hypertrophy and can prevent muscle atrophy in vivo, 10.1038/ncb1101-1014
  73. Pallafacchina G., Calabria E., Serrano A. L., Kalhovde J. M., Schiaffino S., A protein kinase B-dependent and rapamycin-sensitive pathway controls skeletal muscle growth but not fiber type specification, 10.1073/pnas.142166599
  74. Wullschleger Stephan, Loewith Robbie, Hall Michael N., TOR Signaling in Growth and Metabolism, 10.1016/j.cell.2006.01.016
  75. Hay N., Upstream and downstream of mTOR, 10.1101/gad.1212704
  76. Ma Xiaoju Max, Blenis John, Molecular mechanisms of mTOR-mediated translational control, 10.1038/nrm2672
  77. Tee Andrew R., Blenis John, mTOR, translational control and human disease, 10.1016/j.semcdb.2004.11.005
  78. Meyuhas Oded, Synthesis of the translational apparatus is regulated at the translational level : TOP mRNAs and the translational apparatus, 10.1046/j.1432-1327.2000.01719.x
  79. Hannan K. M., Brandenburger Y., Jenkins A., Sharkey K., Cavanaugh A., Rothblum L., Moss T., Poortinga G., McArthur G. A., Pearson R. B., Hannan R. D., mTOR-Dependent Regulation of Ribosomal Gene Transcription Requires S6K1 and Is Mediated by Phosphorylation of the Carboxy-Terminal Activation Domain of the Nucleolar Transcription Factor UBF , 10.1128/mcb.23.23.8862-8877.2003
  80. Morissette Michael R., Cook Stuart A., Buranasombati Cattleya, Rosenberg Michael A., Rosenzweig Anthony, Myostatin inhibits IGF-I-induced myotube hypertrophy through Akt, 10.1152/ajpcell.00043.2009
  81. Lipina Christopher, Kendall Hannah, McPherron Alexandra C., Taylor Peter M., Hundal Harinder S., Mechanisms involved in the enhancement of mammalian target of rapamycin signalling and hypertrophy in skeletal muscle of myostatin-deficient mice, 10.1016/j.febslet.2010.04.039
  82. Suryawan Agus, Frank Jason W, Nguyen Hanh V, Davis Teresa A, Expression of the TGF-β Family of Ligands Is Developmentally Regulated in Skeletal Muscle of Neonatal Rats, 10.1203/01.pdr.0000196718.47935.6e
  83. Welle Stephen, Bhatt Kirti, Pinkert Carl A., Myofibrillar protein synthesis in myostatin-deficient mice, 10.1152/ajpendo.00433.2005
  84. Welle Stephen, Burgess Kerri, Mehta Sangeeta, Stimulation of skeletal muscle myofibrillar protein synthesis, p70 S6 kinase phosphorylation, and ribosomal protein S6 phosphorylation by inhibition of myostatin in mature mice, 10.1152/ajpendo.90862.2008
  85. Steelman CA, Recknor JC, Nettleton D, Reecy JM (2006) Transcriptional profiling of myostatin-knockout mice implicates Wnt signaling in postnatal skeletal muscle growth and hypertrophy. FASEB J 20(3):580–582. doi: 10.1096/fj.05-5125fje
  86. Csibi Alfredo, Cornille Karen, Leibovitch Marie-Pierre, Poupon Anne, Tintignac Lionel A., Sanchez Anthony M. J., Leibovitch Serge A., The Translation Regulatory Subunit eIF3f Controls the Kinase-Dependent mTOR Signaling Required for Muscle Differentiation and Hypertrophy in Mouse, 10.1371/journal.pone.0008994
  87. Lagirand-Cantaloube Julie, Offner Nicolas, Csibi Alfredo, Leibovitch Marie P, Batonnet-Pichon Sabrina, Tintignac Lionel A, Segura Carlos T, Leibovitch Serge A, The initiation factor eIF3-f is a major target for Atrogin1/MAFbx function in skeletal muscle atrophy, 10.1038/emboj.2008.52
  88. Mayhew David L., Hornberger Troy A., Lincoln Hannah C., Bamman Marcas M., Eukaryotic initiation factor 2B epsilon induces cap-dependent translation and skeletal muscle hypertrophy : eIF2Bɛ induces skeletal muscle hypertrophy, 10.1113/jphysiol.2010.202432
  89. Sandri Marco, Sandri Claudia, Gilbert Alex, Skurk Carsten, Calabria Elisa, Picard Anne, Walsh Kenneth, Schiaffino Stefano, Lecker Stewart H, Goldberg Alfred L, Foxo Transcription Factors Induce the Atrophy-Related Ubiquitin Ligase Atrogin-1 and Cause Skeletal Muscle Atrophy, 10.1016/s0092-8674(04)00400-3
  90. Stitt Trevor N., Drujan Doreen, Clarke Brian A., Panaro Frank, Timofeyva Yekatarina, Kline William O., Gonzalez Michael, Yancopoulos George D., Glass David J., The IGF-1/PI3K/Akt Pathway Prevents Expression of Muscle Atrophy-Induced Ubiquitin Ligases by Inhibiting FOXO Transcription Factors, 10.1016/s1097-2765(04)00211-4
  91. McFarlane Craig, Plummer Erin, Thomas Mark, Hennebry Alex, Ashby Murray, Ling Nicholas, Smith Heather, Sharma Mridula, Kambadur Ravi, Myostatin induces cachexia by activating the ubiquitin proteolytic system through an NF-κB-independent, FoxO1-dependent mechanism, 10.1002/jcp.20757
  92. Allen David L., Unterman Terry G., Regulation of myostatin expression and myoblast differentiation by FoxO and SMAD transcription factors, 10.1152/ajpcell.00542.2005
  93. Lokireddy Sudarsanareddy, Mouly Vincent, Butler-Browne Gillian, Gluckman Peter D., Sharma Mridula, Kambadur Ravi, McFarlane Craig, Myostatin promotes the wasting of human myoblast cultures through promoting ubiquitin-proteasome pathway-mediated loss of sarcomeric proteins, 10.1152/ajpcell.00114.2011
  94. Lokireddy Sudarsanareddy, Wijesoma Isuru Wijerupage, Sze Siu Kwan, McFarlane Craig, Kambadur Ravi, Sharma Mridula, Identification of atrogin-1-targeted proteins during the myostatin-induced skeletal muscle wasting, 10.1152/ajpcell.00402.2011
  95. Mendias Christopher L., Kayupov Erdan, Bradley Joshua R., Brooks Susan V., Claflin Dennis R., Decreased specific force and power production of muscle fibers from myostatin-deficient mice are associated with a suppression of protein degradation, 10.1152/japplphysiol.00126.2011
  96. Sriram Sandhya, Subramanian Subha, Juvvuna Prasanna Kumar, Ge Xiaojia, Lokireddy Sudarsanareddy, McFarlane Craig Desmond, Wahli Walter, Kambadur Ravi, Sharma Mridula, Myostatin Augments Muscle-Specific Ring Finger Protein-1 Expression Through an NF-kB Independent Mechanism in SMAD3 Null Muscle, 10.1210/me.2013-1179
  97. Zhou Xiaolan, Wang Jin Lin, Lu John, Song Yanping, Kwak Keith S., Jiao Qingsheng, Rosenfeld Robert, Chen Qing, Boone Thomas, Simonet W. Scott, Lacey David L., Goldberg Alfred L., Han H.Q., Reversal of Cancer Cachexia and Muscle Wasting by ActRIIB Antagonism Leads to Prolonged Survival, 10.1016/j.cell.2010.07.011
  98. Lee Jen Y., Hopkinson Nicholas S., Kemp Paul R., Myostatin induces autophagy in skeletal muscle in vitro, 10.1016/j.bbrc.2011.10.124
  99. Seiliez Iban, Taty Taty Gémaël Cédrick, Bugeon Jérôme, Dias Karine, Sabin Nathalie, Gabillard Jean-Charles, Myostatin induces atrophy of trout myotubes through inhibiting the TORC1 signaling and promoting Ubiquitin–Proteasome and Autophagy-Lysosome degradative pathways, 10.1016/j.ygcen.2013.02.008
  100. Garikipati Dilip K., Rodgers Buel D., Myostatin stimulates myosatellite cell differentiation in a novel model system: evidence for gene subfunctionalization, 10.1152/ajpregu.00523.2011
Bibliographic reference Rodriguez, Julie ; Vernus, Barbara ; Chelh, Ilham ; Cassar-Malek, Isabelle ; Gabillard, Jean-Charles ; et. al. Myostatin and the skeletal muscle atrophy and hypertrophy signaling pathways.. In: Cellular and molecular life sciences, Vol. 71, no.22, p. 4361-4371 (2014)
Permanent URL http://hdl.handle.net/2078/218719