Isolation, Culture, Identification, and Bioenergetics Metabolism of Equine Skeletal Muscle Satellite Cells
Culture and Characteristic of Equine Satellite Cells
Keywords:
equine, muscle satellite cells, isolation, bioenergetics metabolismAbstract
Equine skeletal muscle satellite cells (EMSCs) are muscle stem cells in horses, responsible for the postnatal growth, repair, and homeostasis of skeletal muscles. EMSCs are an attractive model for horses to investigate the mechanisms of muscle growth and spontaneously fuse to form differentiated muscle fiber types through activating a battery of muscle-specific genes. Previous reports on the successful isolation and culture of skeletal muscle satellite cells mostly used skeletal muscles of young animals. With the high value of horses, skeletal muscle samples of foals are very difficult to obtain. The present study describes protocols for enriching the satellite cell fraction from the semitendinosus of a 2-year-old Mongolian horse to isolate the EMSCs. Optimized culture conditions with gelatin layering accelerated the adhesion speed of EMSCs. The identification of EMSCs was carried out through multiple dimensions including cell morphology, myogenic induction, differential adhering, and molecular signatures. In particular, the Seahorse Extracellular Flux analyzer was utilized for evaluating the bioenergetics metabolism of EMSCs by measuring the oxygen consumption rate (OCR) and extracellular acidification rate (ECAR). The present study provides reference for the isolation, purification, identification, and bioenergetics metabolism characteristics of EMSCs, which would be useful for studying the molecular mechanisms for muscle development, muscle fiber type differentiation, and recovery from muscle injury in horses.
References
Gurgul A, Jasielczuk I, Semik-Gurgul E, Pawlina-Tyszko K, Stefaniuk-Szmukier M, Szmatoła T, et al. A genome-wide scan for diversifying selection signatures in selected horse breeds. PLoS One 2019;14:e0210751. https://doi.org/10.1371/journal.pone.0210751.
Mickelson JR, Valberg SJ. The genetics of skeletal muscle disorders in horses. Annu Rev Anim Biosci 2015;3:197–217. https://doi.org/10.1146/annurev-animal-022114-110653.
Zammit PS. All muscle satellite cells are equal, but are some more equal than others? J Cell Sci 2008;121:2975–82. https://doi.org/10.1242/jcs.019661.
Di Foggia V, Robson L. Isolation of satellite cells from single muscle fibers from young, aged, or dystrophic muscles. Methods Mol Biol 2012;916:3–14. https://doi.org/10.1007/978-1-61779-980-8_1.
Morgan JE, Partridge TA. Muscle satellite cells. The International Journal of Biochemistry & Cell Biology 2003;35:1151–6. https://doi.org/10.1016/S1357-2725(03)00042-6.
Williams CA. The effect of oxidative stress during exercise in the horse. J Anim Sci 2016;94:4067–75. https://doi.org/10.2527/jas.2015-9988.
Mami S, Khaje G, Shahriari A, Gooraninejad S. Evaluation of biological indicators of fatigue and muscle damage in Arabian horses after race. J Equine Vet Sci 2019;78:74–8. https://doi.org/10.1016/j.jevs.2019.04.007.
Marlin DJ, Fenn K, Smith N, Deaton CD, Roberts CA, Harris PA, et al. Changes in circulatory antioxidant status in horses during prolonged exercise. J Nutr 2002;132:1622S-7S. https://doi.org/10.1093/jn/132.6.1622S.
Schienda J, Engleka KA, Jun S, Hansen MS, Epstein JA, Tabin CJ, et al. Somitic origin of limb muscle satellite and side population cells. Proc Natl Acad Sci U S A 2006;103:945–50. https://doi.org/10.1073/pnas.0510164103.
Fukada S, Ma Y, Ohtani T, Watanabe Y, Murakami S, Yamaguchi M. Isolation, characterization, and molecular regulation of muscle stem cells. Front Physiol 2013;4:317. https://doi.org/10.3389/fphys.2013.00317.
Rhoads RP, Fernyhough ME, Liu X, McFarland DC, Velleman SG, Hausman GJ, et al. Extrinsic regulation of domestic animal-derived myogenic satellite cells II. Domestic Animal Endocrinology 2009;36:111–26. https://doi.org/10.1016/j.domaniend.2008.12.005.
Mauro A. Satellite cell of skeletal muscle fibers. J Biophys Biochem Cytol 1961;9:493–5. https://doi.org/10.1083/jcb.9.2.493.
Bennett VD, Cowles E, Husic HD, Suelter CH. Muscle cell cultures from chicken breast muscle have increased specific activities of creatine kinase when incubated at 41 degrees C compared with 37 degrees C. Exp Cell Res 1986;164:63–70. https://doi.org/10.1016/0014-4827(86)90454-4.
Dodson MV, Martin EL, Brannon MA, Mathison BA, McFarland DC. Optimization of bovine satellite cell-derived myotube formation in vitro. Tissue Cell 1987;19:159–66. https://doi.org/10.1016/0040-8166(87)90001-2.
Wu H, Ren Y, Li S, Wang W, Yuan J, Guo X, et al. In vitro culture and induced differentiation of sheep skeletal muscle satellite cells. Cell Biol Int 2012;36:579–87. https://doi.org/10.1042/CBI20110487.
Li B, Li P, Huang R, Sun W, Wang H, Li Q, et al. Isolation, culture and identification of porcine skeletal muscle satellite cells. Asian-Australas J Anim Sci 2015;28:1171–7. https://doi.org/10.5713/ajas.14.0848.
Gibson MC, Schultz E. Age-related differences in absolute numbers of skeletal muscle satellite cells. Muscle Nerve 1983;6:574–80. https://doi.org/10.1002/mus.880060807.
Greene EA, Raub RH. Procedures for harvesting satelite cells from equine skeletal muscle. Journal of Equine Veterinary Science 1992;12:33–5. https://doi.org/10.1016/S0737-0806(06)81383-3.
Folmes CDL, Dzeja PP, Nelson TJ, Terzic A. Metabolic plasticity in stem cell homeostasis and differentiation. Cell Stem Cell 2012;11:596–606. https://doi.org/10.1016/j.stem.2012.10.002.
Verdijk LB, Snijders T, Drost M, Delhaas T, Kadi F, van Loon LJC. Satellite cells in human skeletal muscle; from birth to old age. Age (Dordr) 2014;36:545–7. https://doi.org/10.1007/s11357-013-9583-2.
Livak KJ, Schmittgen TD. Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method. Methods 2001;25:402–8. https://doi.org/10.1006/meth.2001.1262.
Miersch C, Stange K, Röntgen M. Separation of functionally divergent muscle precursor cell populations from porcine juvenile muscles by discontinuous Percoll density gradient centrifugation. BMC Cell Biology 2018;19:2. https://doi.org/10.1186/s12860-018-0156-1.
Rosenblatt JD, Lunt AI, Parry DJ, Partridge TA. Culturing satellite cells from living single muscle fiber explants. In Vitro Cell Dev Biol Anim 1995;31:773–9. https://doi.org/10.1007/BF02634119.
Mesires NT, Doumit ME. Satellite cell proliferation and differentiation during postnatal growth of porcine skeletal muscle. Am J Physiol Cell Physiol 2002;282:C899-906. https://doi.org/10.1152/ajpcell.00341.2001.
Wilschut KJ, Jaksani S, Van Den Dolder J, Haagsman HP, Roelen BAJ. Isolation and characterization of porcine adult muscle-derived progenitor cells. J Cell Biochem 2008;105:1228–39. https://doi.org/10.1002/jcb.21921.
Gharaibeh B, Lu A, Tebbets J, Zheng B, Feduska J, Crisan M, et al. Isolation of a slowly adhering cell fraction containing stem cells from murine skeletal muscle by the preplate technique. Nat Protoc 2008;3:1501–9. https://doi.org/10.1038/nprot.2008.142.
Kim KH, Qiu J, Kuang S. Isolation, Culture, and Differentiation of primary myoblasts derived from muscle satellite cells. Bio Protoc 2020;10:e3686. https://doi.org/10.21769/BioProtoc.3686.
Bai C, Hou L, Li F, He X, Zhang M, Guan W. Isolation and biological characteristics of beijing Fatty chicken skeletal muscle satellite cells. Cell Commun Adhes 2012;19:69–77. https://doi.org/10.3109/15419061.2012.743998.
Bian Y, Mu R, Li X, Li Y, Guan W. Isolation and biological characteristics of skeletal muscle satellite cells of Luxi cattle embryo. Journal of Huazhong Agricultural University 2013;32:90–6.
Siegel AL, Atchison K, Fisher KE, Davis GE, Cornelison DDW. 3D timelapse analysis of muscle satellite cell motility. Stem Cells 2009;27:2527–38. https://doi.org/10.1002/stem.178.
Wang Y, Dai Y, Liu XF, Liu ZW, Li JX, Guo H, et al. Isolation, identification and induced differentiation of bovine skeletal muscle satellite cells. Chinese Journal of Animal Science and Veterinary Medicine 2014;41:142–7.
Danoviz ME, Yablonka-Reuveni Z. Skeletal muscle satellite cells: background and methods for isolation and analysis in a primary culture system. Methods Mol Biol 2012;798:21–52. https://doi.org/10.1007/978-1-61779-343-1_2.
Stratos I, Rotter R, Eipel C, Mittlmeier T, Vollmar B. Granulocyte-colony stimulating factor enhances muscle proliferation and strength following skeletal muscle injury in rats. J Appl Physiol (1985) 2007;103:1857–63. https://doi.org/10.1152/japplphysiol.00066.2007.
Kanisicak O, Mendez JJ, Yamamoto S, Yamamoto M, Goldhamer DJ. Progenitors of skeletal muscle satellite cells express the muscle determination gene, MyoD. Dev Biol 2009;332:131–41. https://doi.org/10.1016/j.ydbio.2009.05.554.
von Maltzahn J, Jones AE, Parks RJ, Rudnicki MA. Pax7 is critical for the normal function of satellite cells in adult skeletal muscle. Proceedings of the National Academy of Sciences 2013;110:16474–9. https://doi.org/10.1073/pnas.1307680110.
Tedesco FS, Dellavalle A, Diaz-Manera J, Messina G, Cossu G. Repairing skeletal muscle: regenerative potential of skeletal muscle stem cells. J Clin Invest 2010;120:11–9. https://doi.org/10.1172/JCI40373.
Hernández-Hernández JM, García-González EG, Brun CE, Rudnicki MA. The myogenic regulatory factors, determinants of muscle development, cell identity and regeneration. Semin Cell Dev Biol 2017;72:10–8. https://doi.org/10.1016/j.semcdb.2017.11.010.
Jeong J, Choi K-H, Kim S-H, Lee D-K, Oh J-N, Lee M, et al. Combination of cell signaling molecules can facilitate MYOD1-mediated myogenic transdifferentiation of pig fibroblasts. J Anim Sci Biotechnol 2021;12:64. https://doi.org/10.1186/s40104-021-00583-1.
Yang J, Liu H, Wang K, Li L, Yuan H, Liu X, et al. Isolation, culture and biological characteristics of multipotent porcine skeletal muscle satellite cells. Cell Tissue Bank 2017;18:513–25. https://doi.org/10.1007/s10561-017-9614-9.
Allen RE. Muscle cell growth and development. Designing Foods, Washington, DC: National Research Council National Academy Press; 1988, p. 142–62.
Bao T, Han H, Li B, Zhao Y, Bou G, Zhang X, et al. The distinct transcriptomes of fast-twitch and slow-twitch muscles in Mongolian horses. Comparative Biochemistry and Physiology Part D: Genomics and Proteomics 2020;33:100649. https://doi.org/10.1016/j.cbd.2019.100649.
Schiaffino S, Reggiani C. Fiber types in mammalian skeletal muscles. Physiol Rev 2011;91:1447–531. https://doi.org/10.1152/physrev.00031.2010.
Seene T, Kaasik P, Alev K, Pehme A, Riso EM. Composition and turnover of contractile proteins in volume-overtrained skeletal muscle. Int J Sports Med 2004;25:438–45. https://doi.org/10.1055/s-2004-820935.
White SH, Wohlgemuth S, Li C, Warren LK. Rapid Communication: Dietary selenium improves skeletal muscle mitochondrial biogenesis in young equine athletes. J Anim Sci 2017;95:4078–84. https://doi.org/10.2527/jas2017.1919.
Shamim B, Hawley JA, Camera DM. Protein availability and satellite cell dynamics in skeletal muscle. Sports Med 2018;48:1329–43. https://doi.org/10.1007/s40279-018-0883-7.
Hearne A, Chen H, Monarchino A, Wiseman JS. Oligomycin-induced proton uncoupling. Toxicology in Vitro 2020;67:104907. https://doi.org/10.1016/j.tiv.2020.104907.
Smolina N, Bruton J, Kostareva A, Sejersen T. Assaying mitochondrial respiration as an indicator of cellular metabolism and fitness. Methods Mol Biol 2017;1601:79–87. https://doi.org/10.1007/978-1-4939-6960-9_7.
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