Inception and Significance of Myoblasts

Authors

  • Dr. Senthilkumar Rajagopal

Keywords:

Myofibril, cytokines, skeletal system, Hepatocytes, Myostatin

Abstract

Adult mammalian skeletal muscle regeneration involves many proteins and signalling networks. Cytokines influence skeletal muscle development. Myofibrillar repair and regeneration depend on cytokines generated by cells of immune system, at injury site of muscle. Skeletal muscle is a key generator of cytokines. Muscle-released cytokines (myokines) may have endocrine effects on regulation of metabolism. Available reports suggest that myogenic differentiation and regeneration are governed by autocrine cytokines released by muscles. Present review focus on cytokines that (a) expression of muscle cells and (b) have a myogenic role. This group of cytokines controls the entire myogenic process. How cytokines create a regulatory network is an intriguing and crucial topic. To fully explore the therapeutic potential of cytokines, functional studies must pinpoint their in vivo source.

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References

Montarras, D., L'honoré, A. and Buckingham, M. Lying low but ready for action: the quiescent muscle satellite cell. The FEBS journal, 280(17), pp.4036-4050, 2013.

Buckingham, M. and Rigby, P.W. Gene regulatory networks and transcriptional mechanisms that control myogenesis. Developmental cell, 28(3), pp.225-238, 2014.

Simionescu, A. and Pavlath, G.K. Molecular mechanisms of myoblast fusion across species. Cell Fusion in Health and Disease, pp.113-135, 2011.

Tidball, J.G. Regulation of muscle growth and regeneration by the immune system. Nature Reviews Immunology, 17(3), pp.165-178, 2017.

Whitham, M. and Febbraio, M.A. The ever-expanding myokinome: discovery challenges and therapeutic implications. Nature reviews Drug discovery, 15(10), pp.719-729, 2016.

Peake, J., Della Gatta, P., Suzuki, K. and Nieman, D. Cytokine expression and secretion by skeletal muscle cells: regulatory mechanisms and exercise effects. Exercise immunology review, 21, pp.8-25, 2015.

Yartseva, V., Goldstein, L.D., Rodman, J., Kates, L., Chen, M.Z., Chen, Y.J.J., Foreman, O., Siebel, C.W., Modrusan, Z., Peterson, A.S. and Jovičić, A. Heterogeneity of satellite cells implicates DELTA1/NOTCH2 signaling in self-renewal. Cell Reports, 30(5), pp.1491-1503, 2020.

Oprescu, S.N., Yue, F., Qiu, J., Brito, L.F. and Kuang, S. Temporal dynamics and heterogeneity of cell populations during skeletal muscle regeneration. IScience, 23(4) , 2020.

Dell'Orso, S., Juan, A.H., Ko, K.D., Naz, F., Perovanovic, J., Gutierrez-Cruz, G., Feng, X. and Sartorelli, V. Single cell analysis of adult mouse skeletal muscle stem cells in homeostatic and regenerative conditions. Development, 146(12), p.dev174177, 2019.

De Micheli, A.J., Laurilliard, E.J., Heinke, C.L., Ravichandran, H., Fraczek, P., Soueid-Baumgarten, S., De Vlaminck, I., Elemento, O. and Cosgrove, B.D. Single-cell analysis of the muscle stem cell hierarchy identifies heterotypic communication signals involved in skeletal muscle regeneration. Cell reports, 30(10), pp.3583-3595, 2020.

Masui, O., Krakovska, O., Belozerov, V.E., Voisin, S., Ghanny, S., Chen, J., Moyez, D., Zhu, P., Evans, K.R., McDermott, J.C. and Siu, K.M. Identification of differentially regulated secretome components during skeletal myogenesis. Molecular & Cellular Proteomics, 10(5) , 2011.

Henningsen, J., Pedersen, B.K. and Kratchmarova, I. Quantitative analysis of the secretion of the MCP family of chemokines by muscle cells. Molecular BioSystems, 7(2), pp.311-321, 2011.

Henningsen, J., Rigbolt, K.T., Blagoev, B., Pedersen, B.K. and Kratchmarova, I. Dynamics of the skeletal muscle secretome during myoblast differentiation. Molecular & cellular proteomics, 9(11), pp.2482-2496, 2010.

Yoon, J.H., Yea, K., Kim, J., Choi, Y.S., Park, S., Lee, H., Lee, C.S., Suh, P.G. and Ryu, S.H. Comparative proteomic analysis of the insulin‐induced L6 myotube secretome. Proteomics, 9(1), pp.51-60, 2009.

Norheim, F., Raastad, T., Thiede, B., Rustan, A.C., Drevon, C.A. and Haugen, F. Proteomic identification of secreted proteins from human skeletal muscle cells and expression in response to strength training. American Journal of Physiology-Endocrinology and Metabolism, 301(5), pp.E1013-E1021, 2011.

Griffin, C.A., Apponi, L.H., Long, K.K. and Pavlath, G.K. Chemokine expression and control of muscle cell migration during myogenesis. Journal of cell science, 123(18), pp.3052-3060, 2010.

Waldemer‐Streyer, R.J., Kim, D. and Chen, J. Muscle cell‐derived cytokines in skeletal muscle regeneration. The FEBS Journal, 289(21), pp.6463-6483, 2022.

Florini, J.R., Ewton, D.Z. and Coolican, S.A. Growth hormone and the insulin-like growth factor system in myogenesis. Endocrine reviews, 17(5), pp.481-517, 1996.

Florini, J.R., Ewton, D.Z. and Magri, K.A. Hormones, growth factors, and myogenic differentiation. Annual review of physiology, 53(1), pp.201-216, 1991.

Stewart, C.E. and Rotwein, P. Growth, differentiation, and survival: multiple physiological functions for insulin-like growth factors. Physiological reviews, 76(4), pp.1005-1026, 1996.

Saini, A., Nasser, A.S. and Stewart, C.E. Waste management—cytokines, growth factors and cachexia. Cytokine & growth factor reviews, 17(6), pp.475-486, 2006.

Glass, D.J. Molecular mechanisms modulating muscle mass. Trends in molecular medicine, 9(8), pp.344-350, 2003.

Florini, J.R., Magri, K.A., Ewton, D.Z., James, P.L., Grindstaff, K. and Rotwein, P.S. “Spontaneous” differentiation of skeletal myoblasts is dependent upon autocrine secretion of insulin-like growth factor-II. Journal of Biological Chemistry, 266(24), pp.15917-15923, 1991.

Tollefsen, S.E., Lajara, R., McCusker, R.H., Clemmons, D.R. and Rotwein, P. Insulin-like growth factors (IGF) in muscle development: Expression of IGF-I, the IGF-I receptor, and an IGF binding protein during myoblast differentiation. Journal of Biological Chemistry, 264(23), pp.13810-13817, 1989.

Tollefsen, S.E., Sadow, J.L. and Rotwein, P. Coordinate expression of insulin-like growth factor II and its receptor during muscle differentiation. Proceedings of the National Academy of Sciences, 86(5), pp.1543-1547, 1989.

Pawlikowski, B., Vogler, T.O., Gadek, K. and Olwin, B.B. Regulation of skeletal muscle stem cells by fibroblast growth factors. Developmental Dynamics, 246(5), pp.359-367, 2017.

Yablonka-Reuveni, Z., Balestreri, T.M. and Bowen-Pope, D.F. Regulation of proliferation and differentiation of myoblasts derived from adult mouse skeletal muscle by specific isoforms of PDGF. The Journal of cell biology, 111(4), pp.1623-1629, 1990.

Jin, P., Sejersen, T. and Ringertz, N.R. Recombinant platelet-derived growth factor-BB stimulates growth and inhibits differentiation of rat L6 myoblasts. Journal of Biological Chemistry, 266(2), pp.1245-1249, 1991.

Sejersen, T., Betsholtz, C., Sjölund, M., Heldin, C.H., Westermark, B. and Thyberg, J. Rat skeletal myoblasts and arterial smooth muscle cells express the gene for the A chain but not the gene for the B chain (c-sis) of platelet-derived growth factor (PDGF) and produce a PDGF-like protein. Proceedings of the National Academy of Sciences, 83(18), pp.6844-6848, 1986.

Jennische, E., Ekberg, S.T.A.F.F.A.N. and Matejka, G.L. Expression of hepatocyte growth factor in growing and regenerating rat skeletal muscle. American Journal of Physiology-Cell Physiology, 265(1), pp.C122-C128, 1993.

Florini, J.R., Ewton, D.Z. and Magri, K.A. Hormones, growth factors, and myogenic differentiation. Annual review of physiology, 53(1), pp.201-216, 1991.

Massagué, J., Cheifetz, S., Endo, T. and Nadal-Ginard, B. Type beta transforming growth factor is an inhibitor of myogenic differentiation. Proceedings of the National Academy of Sciences, 83(21), pp.8206-8210, 1986.

Olson, E.N., Sternberg, E., Hu, J.S., Spizz, G. and Wilcox, C. Regulation of myogenic differentiation by type beta transforming growth factor. The Journal of cell biology, 103(5), pp.1799-1805, 1986.

Rodgers, B.D., Wiedeback, B.D., Hoversten, K.E., Jackson, M.F., Walker, R.G. and Thompson, T.B. Myostatin stimulates, not inihibits, C2C12 myoblast proliferation. Endocrinology, 155(3), pp.670-675, 2014.

Schabort, E.J., van der Merwe, M., Loos, B., Moore, F.P. and Niesler, C.U. TGF-β's delay skeletal muscle progenitor cell differentiation in an isoform-independent manner. Experimental cell research, 315(3), pp.373-384, 2009.

Liu, D., Black, B.L. and Derynck, R. TGF-β inhibits muscle differentiation through functional repression of myogenic transcription factors by Smad3. Genes & development, 15(22), pp.2950-2966, 2001.

Lafyatis R, Lechleider R, Roberts AB, Sporn MB. Secretion and transcriptional regulation of transforming growth factor-beta 3 during myogenesis. Molecular and cellular biology. 1991.

McPherron, A.C., Lawler, A.M. and Lee, S.J. Regulation of skeletal muscle mass in mice by a new TGF-p superfamily member. Nature, 387(6628), pp.83-90, 1997.

Rodgers, B.D. and Garikipati, D.K. Clinical, agricultural, and evolutionary biology of myostatin: a comparative review. Endocrine reviews, 29(5), pp.513-534, 2008.

Link, B.A. and Nishi, R. Opposing effects of activin A and follistatin on developing skeletal muscle cells. Experimental cell research, 233(2), pp.350-362, 1997.

Egerman, M.A., Cadena, S.M., Gilbert, J.A., Meyer, A., Nelson, H.N., Swalley, S.E., Mallozzi, C., Jacobi, C., Jennings, L.L., Clay, I. and Laurent, G. GDF11 increases with age and inhibits skeletal muscle regeneration. Cell metabolism, 22(1), pp.164-174, 2015.

Rodino‐Klapac, L.R., Haidet, A.M., Kota, J., Handy, C., Kaspar, B.K. and Mendell, J.R. Inhibition of myostatin with emphasis on follistatin as a therapy for muscle disease. Muscle & Nerve: Official Journal of the American Association of Electrodiagnostic Medicine, 39(3), pp.283-296, 2009.

Gilson, H., Schakman, O., Kalista, S., Lause, P., Tsuchida, K. and Thissen, J.P. Follistatin induces muscle hypertrophy through satellite cell proliferation and inhibition of both myostatin and activin. American Journal of Physiology-Endocrinology and Metabolism, 297(1), pp.E157-E164, 2009.

Kota, J., Handy, C.R., Haidet, A.M., Montgomery, C.L., Eagle, A., Rodino-Klapac, L.R., Tucker, D., Shilling, C.J., Therlfall, W.R., Walker, C.M. and Weisbrode, S.E. Follistatin gene delivery enhances muscle growth and strength in nonhuman primates. Science translational medicine, 1(6), pp.6ra15-6ra15, 2009.

Winbanks, C.E., Weeks, K.L., Thomson, R.E., Sepulveda, P.V., Beyer, C., Qian, H., Chen, J.L., Allen, J.M., Lancaster, G.I., Febbraio, M.A. and Harrison, C.A. Follistatin-mediated skeletal muscle hypertrophy is regulated by Smad3 and mTOR independently of myostatin. Journal of Cell Biology, 197(7), pp.997-1008, 2012.

Yahiaoui, L., Gvozdic, D., Danialou, G., Mack, M. and Petrof, B.J. CC family chemokines directly regulate myoblast responses to skeletal muscle injury. The Journal of physiology, 586(16), pp.3991-4004, 2008.

Hara, M., Yuasa, S., Shimoji, K., Onizuka, T., Hayashiji, N., Ohno, Y., Arai, T., Hattori, F., Kaneda, R., Kimura, K. and Makino, S. G-CSF influences mouse skeletal muscle development and regeneration by stimulating myoblast proliferation. Journal of Experimental Medicine, 208(4), pp.715-727, 2011.

Cheng, M., Nguyen, M.H., Fantuzzi, G. and Koh, T.J. Endogenous interferon-γ is required for efficient skeletal muscle regeneration. American Journal of Physiology-Cell Physiology, 294(5), pp.C1183-C1191, 2008.

Otis, J.S., Niccoli, S., Hawdon, N., Sarvas, J.L., Frye, M.A., Chicco, A.J. and Lees, S.J. Pro-inflammatory mediation of myoblast proliferation. PloS one, 9(3), p.e92363, 2014.

Serrano, A.L., Baeza-Raja, B., Perdiguero, E., Jardí, M. and Muñoz-Cánoves, P. Interleukin-6 is an essential regulator of satellite cell-mediated skeletal muscle hypertrophy. Cell metabolism, 7(1), pp.33-44, 2008.

Additional Files

Published

03-03-2024

How to Cite

Dr. Senthilkumar Rajagopal. (2024). Inception and Significance of Myoblasts. Vidhyayana - An International Multidisciplinary Peer-Reviewed E-Journal - ISSN 2454-8596, 9(si2). Retrieved from https://j.vidhyayanaejournal.org/index.php/journal/article/view/1652