J Anim Sci Technol: The roles of growth factors and hormones in the regulation of muscle satellite cells for cultured meat production (original) (raw)
1.
Chriki S, Hocquette JF. The myth of cultured meat: a review. Front Nutr. 2020; 7:7![]()
![]()
![]()
![]()
2.
Handral HK, Tay SH, Chan WW, Choudhury D. 3D Printing of cultured meat products. Crit Rev Food Sci Nutr. 2022; 62:272-81![]()
![]()
![]()
3.
Singh S, Yap WS, Ge XY, Min VLX, Choudhury D. Cultured meat production fuelled by fermentation. Trends Food Sci Technol. 2022; 120:48-58![]()
![]()
4.
Machida S, Spangenburg EE, Booth FW. Primary rat muscle progenitor cells have decreased proliferation and myotube formation during passages. Cell Prolif. 2004; 37:267-77![]()
![]()
![]()
![]()
5.
Ahmad K, Lim JH, Lee EJ, Chun HJ, Ali S, Ahmad SS, et al. Extracellular matrix and the production of cultured meat. Foods. 2021; 10:3116![]()
![]()
![]()
![]()
6.
Piochi M, Micheloni M, Torri L. Effect of informative claims on the attitude of Italian consumers towards cultured meat and relationship among variables used in an explicit approach. Food Res Int. 2022; 151:110881![]()
![]()
![]()
7.
Lee EJ, Jan AT, Baig MH, Ahmad K, Malik A, Rabbani G, et al. Fibromodulin and regulation of the intricate balance between myoblast differentiation to myocytes or adipocyte-like cells. FASEB J. 2018; 32:768-81![]()
![]()
![]()
8.
Choi KH, Yoon JW, Kim M, Lee HJ, Jeong J, Ryu M, et al. Muscle stem cell isolation and in vitro culture for meat production: a methodological review. Compr Rev Food Sci Food Saf. 2021; 20:429-57![]()
![]()
![]()
9.
Johnson SE. NC1184: molecular mechanisms regulating skeletal muscle growth and differentiation. J Anim Sci. 2022; 100:skac229![]()
![]()
![]()
10.
Jan AT, Lee EJ, Ahmad S, Choi I. Meeting the meat: delineating the molecular machinery of muscle development. J Anim Sci Technol. 2016; 58:18![]()
![]()
![]()
![]()
11.
Gastaldello A, Giampieri F, De Giuseppe R, Grosso G, Baroni L, Battino M. The rise of processed meat alternatives: a narrative review of the manufacturing, composition, nutritional profile and health effects of newer sources of protein, and their place in healthier diets. Trends Food Sci Technol. 2022; 127:263-71![]()
![]()
12.
Shaikh S, Lee E, Ahmad K, Ahmad SS, Chun H, Lim J, et al. Cell types used for cultured meat production and the importance of myokines. Foods. 2021; 10:2318![]()
![]()
![]()
![]()
13.
Verbruggen S, Luining D, van Essen A, Post MJ. Bovine myoblast cell production in a microcarriers-based system. Cytotechnology. 2018; 70:503-12![]()
![]()
![]()
![]()
14.
Manassi CF, de Souza SS, Hassemer GS, Sartor S, Lima CMG, Miotto M, et al. Functional meat products: trends in pro-, pre-, syn-, para- and post-biotic use. Food Res Int. 2022; 154:111035![]()
![]()
![]()
15.
Zuk PA, Benhaim P, Hedrick MH. Stem cells from adipose tissue.In In: Lanza R, Gearhart J, Hogan B, Melton D, Pedersen R, Thomson J, West M, editors.editors Handbook of stem cells. Amsterdam: Academic Press. 2004; p p. 425-47![]()
![]()
16.
Ahmad SS, Ahmad K, Lee EJ, Lee YH, Choi I. Implications of insulin-like growth factor-1 in skeletal muscle and various diseases. Cells. 2020; 9:1773![]()
![]()
![]()
![]()
17.
Ding S, Wang F, Liu Y, Li S, Zhou G, Hu P. Characterization and isolation of highly purified porcine satellite cells. Cell Death Discov. 2017; 3:17003![]()
![]()
![]()
![]()
18.
Ding S, Swennen GNM, Messmer T, Gagliardi M, Molin DGM, Li C, et al. Maintaining bovine satellite cells stemness through p38 pathway. Sci Rep. 2018; 8:10808![]()
![]()
![]()
![]()
19.
Bogliotti YS, Wu J, Vilarino M, Okamura D, Soto DA, Zhong C, et al. Efficient derivation of stable primed pluripotent embryonic stem cells from bovine blastocysts. Proc Natl Acad Sci USA. 2018; 115:2090-5![]()
![]()
![]()
![]()
20.
Choi KH, Lee DK, Kim SW, Woo SH, Kim DY, Lee CK. Chemically defined media can maintain pig pluripotency network in vitro. Stem Cell Reports. 2019; 13:221-34![]()
![]()
![]()
![]()
21.
Lee EJ, Jan AT, Baig MH, Ashraf JM, Nahm SS, Kim YW, et al. Fibromodulin: a master regulator of myostatin controlling progression of satellite cells through a myogenic program. FASEB J. 2016; 30:2708-19![]()
![]()
![]()
22.
Ahmad S, Jan AT, Baig MH, Lee EJ, Choi I. Matrix gla protein: an extracellular matrix protein regulates myostatin expression in the muscle developmental program. Life Sci. 2017; 172:55-63![]()
![]()
![]()
23.
Kim T, Ahmad K, Shaikh S, Jan AT, Seo MG, Lee EJ, et al. Dermatopontin in skeletal muscle extracellular matrix regulates myogenesis. Cells. 2019; 8:332![]()
![]()
![]()
![]()
24.
Ahmad K, Lee EJ, Shaikh S, Kumar A, Rao KM, Park SY, et al. Targeting integrins for cancer management using nanotherapeutic approaches: recent advances and challenges. Semin Cancer Biol. 2021; 69:325-36![]()
![]()
![]()
25.
Bomkamp C, Skaalure SC, Fernando GF, Ben-Arye T, Swartz EW, Specht EA. Scaffolding biomaterials for 3D cultivated meat: prospects and challenges. Adv Sci. 2022; 9:2102908![]()
![]()
![]()
![]()
26.
Zhang J, Chen Q, Kaplan DL, Wang Q. High-moisture extruded protein fiber formation toward plant-based meat substitutes applications: science, technology, and prospect. Trends Food Sci Technol. 2022; 128:202-16![]()
![]()
27.
Levi S, Yen FC, Baruch L, Machluf M. Scaffolding technologies for the engineering of cultured meat: towards a safe, sustainable, and scalable production. Trends Food Sci Technol. 2022; 126:13-25![]()
![]()
28.
Listrat A, Lebret B, Louveau I, Astruc T, Bonnet M, Lefaucheur L, et al. How muscle structure and composition influence meat and flesh quality. Sci World J. 2016; 2016:3182746![]()
![]()
![]()
![]()
29.
Fish KD, Rubio NR, Stout AJ, Yuen JSK, Kaplan DL. Prospects and challenges for cell-cultured fat as a novel food ingredient. Trends Food Sci Technol. 2020; 98:53-67![]()
![]()
![]()
![]()
30.
Melzener L, Verzijden KE, Buijs AJ, Post MJ, Flack JE. Cultured beef: from small biopsy to substantial quantity. J Sci Food Agric. 2021; 101:7-14![]()
![]()
![]()
![]()
31.
Reiss J, Robertson S, Suzuki M. Cell sources for cultivated meat: applications and considerations throughout the production workflow. Int J Mol Sci. 2021; 22:7513![]()
![]()
![]()
![]()
32.
Brack AS, Rando TA. Tissue-specific stem cells: lessons from the skeletal muscle satellite cell. Cell Stem Cell. 2012; 10:504-14![]()
![]()
![]()
![]()
33.
Yin H, Price F, Rudnicki MA. Satellite cells and the muscle stem cell niche. Physiol Rev. 2013; 93:23-67![]()
![]()
![]()
![]()
34.
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![]()
![]()
![]()
35.
White TP. Satellite cell and growth factor involvement in skeletal muscle growth. Med Sci Sports Exerc. 1989; 21:S30![]()
![]()
36.
Lee EJ, Pokharel S, Jan AT, Huh S, Galope R, Lim JH, et al. Transthyretin: a transporter protein essential for proliferation of myoblast in the myogenic program. Int J Mol Sci. 2017; 18:115![]()
![]()
![]()
![]()
37.
Vlasova-St. Louis I, Bohjanen PR. Post-transcriptional regulation of cytokine and growth factor signaling in cancer. Cytokine Growth Factor Rev. 2017; 33:83-93![]()
![]()
![]()
![]()
38.
Chen FM, Zhang M, Wu ZF. Toward delivery of multiple growth factors in tissue engineering. Biomaterials. 2010; 31:6279-308![]()
![]()
![]()
39.
Kraemer WJ, Ratamess NA, Hymer WC, Nindl BC, Fragala MS. Growth hormone(s), testosterone, insulin-like growth factors, and cortisol: roles and integration for cellular development and growth with exercise. Front Endocrinol. 2020; 11:33![]()
![]()
![]()
![]()
40.
Yu M, Wang H, Xu Y, Yu D, Li D, Liu X, et al. Insulin-like growth factor-1 (IGF-1) promotes myoblast proliferation and skeletal muscle growth of embryonic chickens via the PI3K/Akt signalling pathway. Cell Biol Int. 2015; 39:910-22![]()
![]()
![]()
41.
Halmos T, Suba I. The physiological role of growth hormone and insulin-like growth factors. Orv Hetil. 2019; 160:1774-83![]()
![]()
![]()
42.
Schmid C, Steiner T, Froesch ER. Preferential enhancement of myoblast differentiation by insulin-like growth factors (IGF I and IGF II) in primary cultures of chicken embryonic cells. FEBS Lett. 1983; 161:117-21![]()
![]()
![]()
43.
Ewton DZ, Florini JR. Effects of the somatomedins and insulin on myoblast differentiation in vitro. Dev Biol. 1981; 86:31-9![]()
![]()
![]()
44.
Huang YC, Dennis RG, Larkin L, Baar K. Rapid formation of functional muscle in vitro using fibrin gels. J Appl Physiol. 2005; 98:706-13![]()
![]()
![]()
45.
Oksbjerg N, Gondret F, Vestergaard M. Basic principles of muscle development and growth in meat-producing mammals as affected by the insulin-like growth factor (IGF) system. Domest Anim Endocrinol. 2004; 27:219-40![]()
![]()
![]()
46.
Massagué J, Cheifetz S, Endo T, Nadal-Ginard B. Type beta transforming growth factor is an inhibitor of myogenic differentiation. Proc Natl Acad Sci USA. 1986; 83:8206-10![]()
![]()
![]()
![]()
47.
Weist MR, Wellington MS, Bermudez JE, Kostrominova TY, Mendias CL, Arruda EM, et al. TGF-β1 enhances contractility in engineered skeletal muscle. J Tissue Eng Regen Med. 2013; 7:562-71![]()
![]()
![]()
![]()
48.
Amit M, Shariki C, Margulets V, Itskovitz-Eldor J. Feeder layer- and serum-free culture of human embryonic stem cells. Biol Reprod. 2004; 70:837-45![]()
![]()
![]()
49.
Rando TA, Blau HM. Primary mouse myoblast purification, characterization, and transplantation for cell-mediated gene therapy. J Cell Biol. 1994; 125:1275-87![]()
![]()
![]()
![]()
50.
Xu C, Rosler E, Jiang J, Lebkowski JS, Gold JD, O’Sullivan C, et al. Basic fibroblast growth factor supports undifferentiated human embryonic stem cell growth without conditioned medium. Stem Cells. 2005; 23:315-23![]()
![]()
![]()
51.
Düsterhöft S, Pette D. Evidence that acidic fibroblast growth factor promotes maturation of rat satellite-cell-derived myotubes in vitro. Differentiation. 1999; 65:161-9![]()
![]()
![]()
52.
Schiaffino S, Mammucari C. Regulation of skeletal muscle growth by the IGF1-Akt/PKB pathway: insights from genetic models. Skelet Muscle. 2011; 1:4![]()
![]()
![]()
![]()
53.
Huang Z, Xu A, Cheung BMY. The potential role of fibroblast growth factor 21 in lipid metabolism and hypertension. Curr Hypertens Rep. 2017; 19:28![]()
![]()
![]()
54.
Liu X, Wang Y, Zhao S, Li X. Fibroblast growth factor 21 promotes C2C12 cells myogenic differentiation by enhancing cell cycle exit. BioMed Res Int. 2017; 2017:1648715![]()
![]()
![]()
![]()
55.
Godoy-Parejo C, Deng C, Liu W, Chen G. Insulin stimulates PI3K/AKT and cell adhesion to promote the survival of individualized human embryonic stem cells. Stem Cells. 2019; 37:1030-41![]()
![]()
![]()
![]()
56.
Tipton KD, Wolfe RR. Exercise, protein metabolism, and muscle growth. Int J Sport Nutr Exerc Metab. 2001; 11:109-32![]()
![]()
![]()
57.
Kumegawa M, Ikeda E, Hosoda S, Takuma T. In vitro effects of thyroxine and insulin on myoblasts from chick embryo skeletal muscle. Dev Biol. 1980; 79:493-9![]()
![]()
![]()
58.
Florini JR, Ewton DZ. Insulin acts as a somatomedin analog in stimulating myoblast growth in serum-free medium. In Vitro. 1981; 17:763-8![]()
![]()
![]()
59.
Miller KJ, Thaloor D, Matteson S, Pavlath GK. Hepatocyte growth factor affects satellite cell activation and differentiation in regenerating skeletal muscle. Am J Physiol Cell Physiol. 2000; 278:C174-81![]()
![]()
![]()
60.
Allen RE, Sheehan SM, Taylor RG, Kendall TL, Rice GM. Hepatocyte growth factor activates quiescent skeletal muscle satellite cells in vitro. J Cell Physiol. 1995; 165:307-12![]()
![]()
![]()
61.
Sinha-Hikim I, Roth SM, Lee MI, Bhasin S. Testosterone-induced muscle hypertrophy is associated with an increase in satellite cell number in healthy, young men. Am J Physiol Endocrinol Metab. 2003; 285:E197-205![]()
![]()
![]()
62.
Herbst KL, Bhasin S. Testosterone action on skeletal muscle. Curr Opin Clin Nutr Metab Care. 2004; 7:271-7![]()
![]()
![]()
63.
Kimura I, Hasegawa T, Ozawa E. Indispensability of iron-bound chick transferrin for chick myogenesis in vitro: (myogenesis/transfrrin/iron). Dev Growth Differ. 1982; 24:369-80![]()
![]()
64.
Mescher AL, Munaim SI. Transferrin and the growth-promoting effect of nerves. Int Rev Cytol. 1988; 110:1-26![]()
![]()
![]()
65.
Matsuda R, Spector D, Micou-Eastwood J, Strohman RC. There is selective accumulation of a growth factor in chicken skeletal muscle. II. Transferrin accumulation in dystrophic fast muscle. Dev Biol. 1984; 103:276-84![]()
![]()
![]()
66.
Simsa R, Yuen J, Stout A, Rubio N, Fogelstrand P, Kaplan DL. Extracellular heme proteins influence bovine myosatellite cell proliferation and the color of cell-based meat. Foods. 2019; 8:521![]()
![]()
![]()
![]()
67.
Suman SP, Joseph P. Myoglobin chemistry and meat color. Annu Rev Food Sci Technol. 2013; 4:79-99![]()
![]()
![]()
68.
Syverud BC, VanDusen KW, Larkin LM. Growth factors for skeletal muscle tissue engineering. Cells Tissues Organs. 2016; 202:169-79![]()
![]()
![]()
![]()
69.
Zhang P, Liang X, Shan T, Jiang Q, Deng C, Zheng R, et al. mTOR is necessary for proper satellite cell activity and skeletal muscle regeneration. Biochem Biophys Res Commun. 2015; 463:102-8![]()
![]()
![]()
![]()
70.
Rion N, Castets P, Lin S, Enderle L, Reinhard JR, Eickhorst C, et al. mTOR controls embryonic and adult myogenesis via mTORC1. Development. 2019; 146:dev172460![]()
![]()
![]()
71.
Gualano B, Roschel H, Lancha AH, Brightbill CE, Rawson ES. In sickness and in health: the widespread application of creatine supplementation. Amino Acids. 2012; 43:519-29![]()
![]()
![]()
72.
Kim J, Lee J, Kim S, Yoon D, Kim J, Sung DJ. Role of creatine supplementation in exercise-induced muscle damage: a mini review. J Exerc Rehabil. 2015; 11:244-50![]()
![]()
![]()
![]()
73.
Yablonka-Reuveni Z, Balestreri TM, Bowen-Pope DF. Regulation of proliferation and differentiation of myoblasts derived from adult mouse skeletal muscle by specific isoforms of PDGF. J Cell Biol. 1990; 111:1623-9![]()
![]()
![]()
![]()
74.
Maley MAL, Davies MJ, Grounds MD. Extracellular matrix, growth factors, genetics: their influence on cell proliferation and myotube formation in primary cultures of adult mouse skeletal muscle. Exp Cell Res. 1995; 219:169-79![]()
![]()
![]()
75.
McFarland DC. Influence of growth factors on poultry myogenic satellite cells. Poult Sci. 1999; 78:747-58![]()
![]()
![]()
76.
Cheung BMY, Deng HB. Fibroblast growth factor 21: a promising therapeutic target in obesity-related diseases. Expert Rev Cardiovasc Ther. 2014; 12:659-66![]()
![]()
![]()
77.
Mossahebi-Mohammadi M, Quan M, Zhang JS, Li X. FGF signaling pathway: a key regulator of stem cell pluripotency. Front Cell Dev Biol. 2020; 8:79![]()
![]()
![]()
![]()
78.
Groux-Muscatelli B, Bassaglia Y, Barritault D, Caruelle JP, Gautron J. Proliferating satellite cells express acidic fibroblast growth factor during in vitro myogenesis. Dev Biol. 1990; 142:380-5![]()
![]()
![]()
79.
Shahini A, Vydiam K, Choudhury D, Rajabian N, Nguyen T, Lei P, et al. Efficient and high yield isolation of myoblasts from skeletal muscle. Stem Cell Res. 2018; 30:122-9![]()
![]()
![]()
![]()
80.
Koledova Z, Sumbal J, Rabata A, de La Bourdonnaye G, Chaloupkova R, Hrdlickova B, et al. Fibroblast growth factor 2 protein stability provides decreased dependence on heparin for induction of FGFR signaling and alters ERK signaling dynamics. Front Cell Dev Biol. 2019; 7:331![]()
![]()
![]()
![]()
81.
Breitkopf K, Roeyen C, Sawitza I, Wickert L, Floege J, Gressner AM. Expression patterns of PDGF-A, -B, -C and -D and the PDGF-receptors α and β in activated rat hepatic stellate cells (HSC). Cytokine. 2005; 31:349-57![]()
![]()
![]()
82.
Albrecht DE, Tidball JG. Platelet-derived growth factor-stimulated secretion of basement membrane proteins by skeletal muscle occurs by tyrosine kinase-dependent and -independent pathways. J Biol Chem. 1997; 272:2236-44![]()
![]()
![]()
83.
Coleman ME, DeMayo F, Yin KC, Lee HM, Geske R, Montgomery C, et al. Myogenic vector expression of insulin-like growth factor I stimulates muscle cell differentiation and myofiber hypertrophy in transgenic mice. J Biol Chem. 1995; 270:12109-16![]()
![]()
![]()
84.
Lawlor MA, Rotwein P. Insulin-like growth factor-mediated muscle cell survival: central roles for Akt and cyclin-dependent kinase inhibitor p21. Mol Cell Biol. 2000; 20:8983-95![]()
![]()
![]()
![]()
85.
Valdés JA, Flores S, Fuentes EN, Osorio-Fuentealba C, Jaimovich E, Molina A. IGF-1 induces IP3-dependent calcium signal involved in the regulation of myostatin gene expression mediated by NFAT during myoblast differentiation. J Cell Physiol. 2013; 228:1452-63![]()
![]()
![]()
86.
Zanou N, Gailly P. Skeletal muscle hypertrophy and regeneration: interplay between the myogenic regulatory factors (MRFs) and insulin-like growth factors (IGFs) pathways. Cell Mol Life Sci. 2013; 70:4117-30![]()
![]()
![]()
87.
Le Roith D. Seminars in medicine of the Beth Israel Deaconess Medical Center. Insulin-like growth factors. N Engl J Med. 1997; 336:633-40![]()
![]()
![]()
88.
Noguchi S. The biological function of insulin-like growth factor-I in myogenesis and its therapeutic effect on muscular dystrophy. Acta Myol. 2005; 24:115-8![]()
89.
McFarland DC, Pesall JE, Gilkerson KK. The influence of growth factors on turkey embryonic myoblasts and satellite cells in vitro. Gen Comp Endocrinol. 1993; 89:415-24![]()
![]()
![]()
90.
Duclos MJ, Wilkie RS, Goddard C. Stimulation of DNA synthesis in chicken muscle satellite cells by insulin and insulin-like growth factors: evidence for exclusive mediation by a type-I insulin-like growth factor receptor. J Endocrinol. 1991; 128:35-42![]()
![]()
![]()
91.
McPherron AC, Lawler AM, Lee SJ. Regulation of skeletal muscle mass in mice by a new TGF-p superfamily member. Nature. 1997; 387:83-90![]()
![]()
![]()
92.
Lee EJ, Ahmad SS, Lim JH, Ahmad K, Shaikh S, Lee YS, et al. Interaction of fibromodulin and myostatin to regulate skeletal muscle aging: an opposite regulation in muscle aging, diabetes, and intracellular lipid accumulation. Cells. 2021; 10:2083![]()
![]()
![]()
![]()
93.
Grobet L, Martin LJR, Poncelet D, Pirottin D, Brouwers B, Riquet J, et al. A deletion in the bovine myostatin gene causes the double–muscled phenotype in cattle. Nat Genet. 1997; 17:71-4![]()
![]()
![]()
94.
Lu J, Sun D, Xu L, Lu G, Zhao F, Wei C, et al. Selection of an effective small interference RNA to silence myostatin gene expression in sheep fibroblast cells. Biochem Genet. 2012; 50:838-47![]()
![]()
![]()
95.
Ahmad SS, Ahmad K, Lee EJ, Shaikh S, Choi I. Computational identification of dithymoquinone as a potential inhibitor of myostatin and regulator of muscle mass. Molecules. 2021; 26:5407![]()
![]()
![]()
![]()
96.
Ali S, Ahmad K, Shaikh S, Lim JH, Chun HJ, Ahmad SS, et al. Identification and evaluation of traditional Chinese medicine natural compounds as potential myostatin inhibitors: an in silico approach. Molecules. 2022; 27:4303![]()
![]()
![]()
![]()
97.
Lee EJ, Shaikh S, Ahmad K, Ahmad SS, Lim JH, Park S, et al. Isolation and characterization of compounds from Glycyrrhiza uralensis as therapeutic agents for the muscle disorders. Int J Mol Sci. 2021; 22:876![]()
![]()
![]()
![]()
98.
Baig MH, Ahmad K, Moon JS, Park SY, Ho Lim J, Chun HJ, et al. Myostatin and its regulation: a comprehensive review of myostatin inhibiting strategies. Front Physiol. 2022; 13:876078![]()
![]()
![]()
![]()
99.
Lee EJ, Shaikh S, Baig MH, Park SY, Lim JH, Ahmad SS, et al. MIF1 and MIF2 myostatin peptide inhibitors as potent muscle mass regulators. Int J Mol Sci. 2022; 23:4222![]()
![]()
![]()
![]()
100.
Delaney K, Kasprzycka P, Ciemerych MA, Zimowska M. The role of TGF-β1 during skeletal muscle regeneration. Cell Biol Int. 2017; 41:706-15![]()
![]()
![]()
101.
Rathbone CR, Yamanouchi K, Chen XK, Nevoret-Bell CJ, Rhoads RP, Allen RE. Effects of transforming growth factor-beta (TGF-β1) on satellite cell activation and survival during oxidative stress. J Muscle Res Cell Motil. 2011; 32:99-109![]()
![]()
![]()
102.
Krieger J, Park BW, Lambert CR, Malcuit C. 3D skeletal muscle fascicle engineering is improved with TGF-β1 treatment of myogenic cells and their co-culture with myofibroblasts. PeerJ. 2018; 6e4939![]()
![]()
![]()
![]()
103.
Ben-Arye T, Levenberg S. Tissue engineering for clean meat production. Front Sustain Food Syst. 2019; 3:46![]()
![]()
104.
Mandel JL, Pearson ML. Insulin stimulates myogenesis in a rat myoblast line. Nature. 1974; 251:618-20![]()
![]()
![]()
105.
Dodson MV, Allen RE, Hossner KL. Ovine somatomedin, multiplication-stimulating activity, and insulin promote skeletal muscle satellite cell proliferation in vitro. Endocrinology. 1985; 117:2357-63![]()
![]()
![]()
106.
Rhoads RP, Baumgard LH, El-Kadi SW, Zhao LD. PHYSIOLOGY AND ENDOCRINOLOGY SYMPOSIUM: roles for insulin-supported skeletal muscle growth. J Anim Sci. 2016; 94:1791-802![]()
![]()
![]()
107.
Kraemer WJ, Ratamess NA, Nindl BC. Recovery responses of testosterone, growth hormone, and IGF-1 after resistance exercise. J Appl Physiol. 2017; 122:549-58![]()
![]()
![]()
108.
Vingren JL, Kraemer WJ, Ratamess NA, Anderson JM, Volek JS, Maresh CM. Testosterone physiology in resistance exercise and training: the up-stream regulatory elements. Sports Med. 2010; 40:1037-53![]()
![]()
![]()
109.
Carson JA, Manolagas SC. Effects of sex steroids on bones and muscles: similarities, parallels, and putative interactions in health and disease. Bone. 2015; 80:67-78![]()
![]()
![]()
![]()
110.
Rossetti ML, Steiner JL, Gordon BS. Androgen-mediated regulation of skeletal muscle protein balance. Mol Cell Endocrinol. 2017; 447:35-44![]()
![]()
![]()
![]()
111.
Munck A, Guyre PM, Holbrook NJ. Physiological functions of glucocorticoids in stress and their relation to pharmacological actions. Endocr Rev. 1984; 5:25-44![]()
![]()
![]()
112.
Sheffield-Moore M, Urban RJ. An overview of the endocrinology of skeletal muscle. Trends Endocrinol Metab. 2004; 15:110-5![]()
![]()
![]()
113.
Boncompagni S, Arthurton L, Akujuru E, Pearson T, Steverding D, Protasi F, et al. Membrane glucocorticoid receptors are localised in the extracellular matrix and signal through the MAPK pathway in mammalian skeletal muscle fibres. J Physiol. 2015; 593:2679-92![]()
![]()
![]()
![]()
114.
Pérez MHA, Cormack J, Mallinson D, Mutungi G. A membrane glucocorticoid receptor mediates the rapid/non-genomic actions of glucocorticoids in mammalian skeletal muscle fibres. J Physiol. 2013; 591:5171-85![]()
![]()
![]()
![]()
115.
Lin JW, Huang YM, Chen YQ, Chuang TY, Lan TY, Liu YW, et al. Dexamethasone accelerates muscle regeneration by modulating kinesin-1-mediated focal adhesion signals. Cell Death Discov. 2021; 7:35![]()
![]()
![]()
![]()
116.
Syverud BC, VanDusen KW, Larkin LM. Effects of dexamethasone on satellite cells and tissue engineered skeletal muscle units. Tissue Eng Part A. 2016; 22:480-9![]()
![]()
![]()
![]()
117.
Guerriero V, Florini JR. Dexamethasone effects on myoblast proliferation and differentiation. Endocrinology. 1980; 106:1198-202![]()
![]()
![]()
118.
Lesmana R, Sinha RA, Singh BK, Zhou J, Ohba K, Wu Y, et al. Thyroid hormone stimulation of autophagy is essential for mitochondrial biogenesis and activity in skeletal muscle. Endocrinology. 2016; 157:23-38![]()
![]()
![]()
119.
Bloise FF, Cordeiro A, Ortiga-Carvalho TM. Role of thyroid hormone in skeletal muscle physiology. J Endocrinol. 2018; 236:R57-68![]()
![]()
![]()
120.
Bloise FF, Oliveira TS, Cordeiro A, Ortiga-Carvalho TM. Thyroid hormones play role in Sarcopenia and Myopathies. Front Physiol. 2018; 9:560![]()
![]()
![]()
![]()
121.
Salvatore D, Simonides WS, Dentice M, Zavacki AM, Larsen PR. Thyroid hormones and skeletal muscle—new insights and potential implications. Nat Rev Endocrinol. 2014; 10:206-14![]()
![]()
![]()
![]()
122.
Martín AI, Priego T, López-Calderón A. Hormones and muscle atrophy. Adv Exp Med Biol. 2018; 1088:207-33![]()
![]()
![]()
123.
Lee EJ, Shaikh S, Choi D, Ahmad K, Baig MH, Lim JH, et al. Transthyretin maintains muscle homeostasis through the novel shuttle pathway of thyroid hormones during myoblast differentiation. Cells. 2019; 8:1565![]()
![]()
![]()
![]()
124.
Bhat ZF, Kumar S, Bhat HF. In vitro meat: a future animal-free harvest. Crit Rev Food Sci Nutr. 2017; 57:782-9![]()
![]()
![]()
125.
Bhat ZF, Bhat H. Animal-free meat biofabrication. Am J Food Technol. 2011; 6:441-59![]()
![]()
126.
Bhatia S, Goli D. Introduction to pharmaceutical biotechnology, volume 1: basic techniques and concepts. Bristol: IOP. 2018![]()
![]()
127.
Verma A. Animal tissue culture: principles and applications.In In: Verma AS, Singh A, editors.editors Animal biotechnology: models in discovery and translation. Amsterdam: Academic Press. 2014; p p. 211-31![]()
128.
van der Valk J, Bieback K, Buta C, Cochrane B, Dirks WG, Fu J, et al. Fetal bovine serum (FBS): past – present – future. Altern Anim Exp. 2018; 35:99-118![]()
![]()
![]()
129.
Bauman E, Granja PL, Barrias CC. Fetal bovine serum-free culture of endothelial progenitor cells—progress and challenges. J Tissue Eng Regen Med. 2018; 12:1567-78![]()
![]()
![]()
130.
Venkatesan M, Semper C, Skrivergaar S, DiLeo R, Mesa N, Rasmussen MK, et al. Recombinant production of growth factors for application in cell culture. iScience. 2022; 25:105054![]()
![]()
![]()
![]()