Growth factors in skeletal muscle regeneration

Cytokine and Growth Factor Reviews

Volumn 7, Issue 3, 1996, Pages 249-258

  Husmann, Irene ^b   Soulet, Laurent ^b   Gautron, Jean ^b   Martelly, Isabelle ^b   Barritault, Denis ^a  

^a UNIVERSITÉ PARIS EST CRÉTEIL   (France)

^b NONE

Author keywords

Differentiation; Growth factor synergy; Growth factors; Regeneration; Skeletal muscle

Indexed keywords

CARRIER PROTEIN; CILIARY NEUROTROPHIC FACTOR; COLONY STIMULATING FACTOR; CYTOKINE; FIBROBLAST GROWTH FACTOR; FIBROBLAST GROWTH FACTOR RECEPTOR; GROWTH FACTOR; GROWTH PROMOTOR; LEUKEMIA INHIBITORY FACTOR; NERVE GROWTH FACTOR; NEUROTROPHIC FACTOR; PLASMINOGEN ACTIVATOR INHIBITOR; PLATELET DERIVED GROWTH FACTOR; PLEIOTROPHIN; PROTEOHEPARAN SULFATE; SCATTER FACTOR; SOMATOMEDIN; SOMATOMEDIN B; SOMATOMEDIN C; TRANSFORMING GROWTH FACTOR BETA;

ANIMAL; CELL DIFFERENTIATION; CELL PROLIFERATION; EXTRACELLULAR MATRIX; HUMAN; MUSCLE DEVELOPMENT; MUSCLE INJURY; MUSCLE REGENERATION; MYOTUBE; NEUROMUSCULAR SYNAPSE; PHYSIOLOGY; PRECURSOR CELL; REGENERATION; SATELLITE CELL; SHORT SURVEY; SKELETAL MUSCLE;

ANIMALS; CARRIER PROTEINS; CYTOKINES; FIBROBLAST GROWTH FACTORS; GROWTH SUBSTANCES; HUMANS; MUSCLE, SKELETAL; PLATELET-DERIVED GROWTH FACTOR; REGENERATION; SOMATOMEDINS;

EID: 0030265501     PISSN: 13596101     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1359-6101(96)00029-9     Document Type: Short Survey

References (108)

1. 1. Mauro A. Satellite cells of skeletal muscle fibres. J Biophys Biochem Cytol 1961, 9, 493-495.
2. 2. Carlson BR, The regeneration of skeletal muscle. A review. Am J Anat 1973, 137, 119-150.
3. 3. Tidball JG. Inflammatory cell response to acute muscle injury. Med Sci Sports Exerc 1995, 27, 1022-1032.
4. 4. Olson EN. Signal transduction pathways that regulate skeletal muscle gene expression. Mol Endocrinol 1993, 7, 1369-1378.
5. 5. Salminen A, Braun T, Jürs S, Winter B, Arnold HH. Transcription of the muscle regulatory gene myf-4 is regulated by serum components, peptide growth factors and signalling pathways involving G proteins. J Cell Biol 1991, 115, 905-917.
6. 6. Li L, Zhou J, James G, Heller-Harrison R, Czech M, Olson EN. FGF inactivates myogenic helix-loop-helix proteins through phosphorylation of a conserved protein kinase C site in their DNA binding domains. Cell 1992, 72, 1181-1194.
7. 7. Grounds MD, Yablonka-Reuveni Z. Molecular and cellular biology of skeletal muscle regeneration. In: Partridge T, ed. Molecular and Cellular Biology of Muscular Dystrophy. Chapman and Hall, London, 1993, pp. 210-257.
8. 8. Allen RE, Dodson MV, Luiten LS. Regulation of skeletal muscle satellite cell proliferation by bovine pituitary fibroblast growth factor. Exp Cell Res 1984, 152, 154-160.
9. 9. Yablonka-Reuveni Z, Rivera AJ. Temporal expression of regulatory and structural muscle proteins during myogenesis of satellite cells on isolated adult rat fibers. Devl Biol 1994, 164, 588-603.
10. 10. Olwin, BB, Rapraeger, A. Repression of myogenic differentiation by aFGF, bFGF, and K-FGF is dependent on cellular heparan sulfate. J Cell Biol 1992, 118, 631-639.
11. 11. Emoto N, Gonzalez AM, Walicke PA, Woda E, Simmons DM, Shimaski S, Baird A. Basic fibroblast growth factor (FGF) in the central nervous system: identification of specific loci of basic FGF expression in the rat brain. Growth Factors 1989, 2, 21-29.
12. 12. Flaumenhaft R, Moscatelli D, Saksela O, Rifkin DB. Role of extracellular matrix in the action of basic fibroblast growth factor: matrix as a source of growth factor for long term stimulation of plasminogen activator production and DNA synthesis. J Cell Physiol 1989, 140, 75-81.
13. 13. DiMario J, Strohmann RC. Satellite cells from dystrophic (mdx) mouse muscle are stimulated by fibroblast growth factor in vitro. Differentiation 1988, 39, 42-49.
14. 14. Anderson JE, Kakulas BA, Jacobsen PF, Johnsen RD, Kornegay JN, Grounds MD. Comparison of basic fibroblast growth factor in X-linked dystrophin-deficient myopathies of human, dog and mouse. Growth Factors 1993, 9, 107-121.
15. 15. Alterio J, Courtois Y, Robelin J, Bechet D, Martelly I. Acidic and basic fibroblast growth factor mRNAs are expressed by skeletal muscle satellite cells. Biochem Biophys Res Commun 1990, 166, 1205-1212.
16. 16. Groux-Muscatelli B, Bassaglia, Y, Barritault D, Caruelle JP, Gautron J. Proliferating satellite cells express acidic fibroblast growth factor during in vitro myogenesis. Devl Biol 1990, 142, 380-385.
17. 17. Grounds MD. Towards understanding skeletal muscle regeneration. Pathol Res Pract 1991, 118, 1-22.
18. 18. Baird A, Ling N. Fibroblast growth factors are present in the extracellular matrix produced by endothelial cells in vitro: implication for a role of heparinase-like enzymes in the neovascular response. Biochem Biophys Res Commun 1987, 142, 428-435.
19. 19. Anderson JE, Liu L, Kardami E. Distinctive patterns of basic fibroblast growth factor (bFGF) distribution in degenerating and regenerating areas of dystrophic (mdx) striated muscles. Devl Biol 1991, 147, 96-109.
20. 20. McLennan I. Localization of transforming growth factor β1 in developing muscles: implications for connective tissue and fiber type pattern formation. Devl Dynamics 1993, 197, 281-290.
21. 21. Joseph-Silverstein J, Consigli SA, Lyser KM, Ver Pault C. Basic fibroblast growth factor in the chick embryo: immunolocalization to striated muscle cells and their precursors. J Cell Biol 1989, 108, 2459-2466.
22. 22. DiMario J, Buffinger N, Yamada S, Strohman RC. Fibroblast growth factor in the extracellular matrix of dystrophic (mdx) mouse muscle. Science 1989, 244, 688-690.
23. 23. Lefaucheur JP, Sébille A. Muscle regeneration following injury can be modified in vivo by immune neutralization of basic fibroblast growth factor, transforming growth factor β1 or insulin-like growth factor I. J Neuroimmunol 1995, 57, 85-91.
24. 24. Rosenthal SM, Brown EJ, Brunetti A, Goldfine JD. Fibroblast growth factor inhibits insulin-like growth factor-II (IGF-II) gene expression and increases IGF-I receptor abundance in BC3H-1 muscle cells. Mol Endocrinol 1991, 5, 678-684.
25. 25. Baird A. Fibroblast growth factors: activities and significance of non-neurotrophin neurotrophic growth factors. Curr Op Neurobiol 1994, 4, 78-86.
26. 26. Yoshida K, Gage FH. Cooperative regulation of nerve growth factor synthesis and secretion in fibroblasts and astrocytes by fibroblast growth factor and other cytokines. Brain Res 1992, 569, 14-25.
27. 27. Unsicker K, Reichert-Preibsch H, Wewetzer K. Stimulation of neuron survival by basic FGF and CNTF is a direct effect and not mediated by non-neuronal cells: Evidence from single cell cultures. Devl Brain Res 1992, 62, 285-288.
28. 28. Gömez-Pinilla F, Cotman CW. Distribution of fibroblast growth factor-5 messenger RNA in the rat brain: an in situ hybridization study. Brain Res 1993, 606, 79-86.
29. 29. Hughes RA, Sendtner M, Goldfarb M, Lindholm D, Thoenen H. Evidence that fibroblast growth factor 5 is a major muscle-derived survival factor for cultured spinal motoneurons. Neuron 1993, 10, 369-377.
30. 30. deLapeyrière O, Rosnet O, Benharroch D, Raybaud F, Marchetto S, Planche J, Galland F, Mattéi MG, Copeland NG, Jenkins NA, Coulier F, Birnbaum D. Structure, chromosome mapping and expression of the murine FGF-6 gene. Oncogene 1990, 5, 823-831.
31. 31. deLapeyrière O, Ollendorff V, Planche J, Ott MO, Pizette S, Coulier F, Birnbaum D. Expression of the FGF6 gene is restricted to developing skeletal muscle in the mouse embryo. Development 1993, 118, 601-611.
32. 32. Mason IJ, Fuller-Pace F, Smith R, Dickson C, FGF-7 (keratinocyte growth factor) expression during mouse development suggests roles in myogenesis, forebrain regionalisation and epithelial-mesenchymal interactions. Mech Dev 1994, 45, 15-30.
33. 33. Johnson DE, Williams LT. Structural and functional diversity in the FGF receptor multigene family. Adv Cancer Res 1993, 60, 1-41.
34. 34. Klagsbrun M, Baird A. A dual receptor system is required for basic fibroblast growth factor activity. Cell 1991, 67, 229-231.
35. 35. Bernfield M, Kokenyesi R, Kato M, Hinkes MT, Spring J, Gallo RL, Lore EJ. Biology of the syndecans: a family of transmembrane heparan sulfate proteoglycans. Ann Rev Cell Biol 1992, 8, 365-393.
36. 36. Burrus LW, Zuber ME, Lueddecke BA, Olwin BB. Identification of a cysteine-rich receptor for fibroblast growth factor. Mol Cell Biol 1992, 12, 156-159.
37. 37. Perderiset M, Courty J, Mereau A, Chevet E, Barritault D. Purification of a heparin binding FGF receptor (HB-FGFR) from adult bovine brain membranes. Biochimie 1992, 74, 1091-1096.
38. 38. Olwin BB, Hauschka SD. Cell surface fibroblast growth factor and epidermal growth factor receptors are permanently lost during skeletal muscle terminal differentiation in culture. J Cell Biol 1988, 107, 761-769.
39. 39. Vaidya TB, Rhodes SJ, Taparowsky EJ, Konieczny SF. Fibroblast growth factor and transforming growth factor β repress transcription of the myogenic regulatory gene MyoD1. Mol Cell Biol 1989, 10, 3934-3944.
40. 40. Yutzey KE, Rhodes SJ, Konieczny SF. Differential transactivation associated with the muscle regulatory factors MyoD1, myogenin, and MRF4. Mol Cell Biol 1990, 10, 3934-3944.
41. 41. Claesson-Welsh L. Platelet-derived growth factor signals. J Biol Chem 1994, 269, 32023-32026.
42. 42. Raines EW, Ross R. Platelet-derived growth factor. I. High yield purification and evidence for multiple forms. J Biol Chem 1982, 257, 5154-5160.
43. 43. Yablonka-Reuveni Z, Balestri 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, 1623-1629.
44. 44. Jin P, Rahm M, Claesson-Wesh L, Heldin C-H, Sejerson T. Expression of PDGF A chain and β-receptor genes during rat myoblast differentiation. J Cell Biol 1990, 110, 1665-1672.
45. 45. Kudla AJ, John ML, Bowen-Pop DF, Rainish B, Olwin BB. A requirement for fibroblast growth factor in regulation of skeletal muscle growth and differentiation cannot be replaced by activation of platelet-derived growth factor signalling pathways. Mol Cell Biol 1995, 15, 3238-3246.
46. 46. Noble M, Murray K, Stroobant P, Waterfield MD, Riddle P. Platelet-derived growth factor promotes division and motility and inhibits premature differentiation of the oligodendrocyte/type 2-astrocyte progenitor cell. Nature 1988, 333, 560-562.
47. 47. Ross R, Raines EW, Bowen-Pope DF. The biology of platelet-derived growth factor. Cell 1986, 46, 156-169.
48. 48. Shimokado K, Raines EW, Madtes DK, Barrett TB, Benditt EP, Ross RA. A significant part of macrophage derived growth factors consists of at least two forms of PDGF. Cell 1985, 43, 277-286.
49. 49. Jodczyk KJ, Bankowski E, Borys A. Stimulatory effect of platelet-breakdown products on muscle regeneration. Zentralbl Allg pathol Anat 1986, 131, 357-361.
50. 50. Assoian R, Sporn MB. Type β transforming growth factors in human platelets: release during platelet granulation and action on vascular smooth muscle cells. J Cell Biol 1986, 102, 1217-1223.
51. 51. Lafyatis R, Lechleider R, Roberts AB, Sporn MB. Secretion and transcriptional regulation of transforming growth factor-beta 3 during myogenesis. Mol Cell Biol 1991, 11, 3795-3803.
52. 52. Wahl SM, Hunt DA, Wakefield LM, McCartney-Francis N, Wahl LM, Roberts AB, Sporn MB. Transforming growth factor β (TGFβ) induces monocyte chemotaxis and growth factor production. Proc Natl Acad Sci USA 1987, 84, 5788-5792.
53. 53. Ignotz RA, Massague J. Transforming growth factor β stimulates the expression of fibronectin and collagen and their incorporation into the extracellular matrix. J Biol Chem 1986, 26, 4337-4345.
54. 54. Roberts AB, Sporn MB, Assoian RK, Smith JM, Roche NS, Wakefield LM, Heine UI, Liotta LA, Falange V, Kehrl JH, Fauci AS. Transforming growth factor: rapid induction of fibrosis and angiogenesis in vivo and stimulation of collagen formation in vitro. Proc Natl Acad Sci USA 1986, 83, 4167-4171.
55. 55. Wisemann DM, Polverini PJ, Kamp DW, Leibovich SJ. Transforming growth factor-beta (TGFβ) is chemotactic for human monocytes and induces their expression of angiogenic activity. Biochem Biophys Res Commun 1988, 157, 793-800.
56. 56. Roberts AB, Joyce ME, Bolander ME, Sporn MB. Transforming growth factor β (TGFβ): a multifunctional effector of both soft and hard tissue regeneration. In: Westermark B, Betsholtz C, Hökfelt B, eds. Growth Factors in Health and Disease: Basic and Clinical Aspects. Exerpta Medica, Amsterdam, 1990, 89-101.
57. 57. Roberts AB, Sporn MB. The transforming growth factor βs. In: Sporn MB, Roberts AB, eds. Peptide Growth Factors and their Receptors I. Basel, Springer, 1990, 419-472.
58. 58. Laiho M, Saksela O, Andreasen PA, Keski-Oja J. Enhanced production and extracellular deposition of the endothelial-type plasminogen activator inhibitor in cultured human lung fibroblasts by transforming growth factor-β. J Cell Biol 1986, 103, 2403-2410.
59. 59. Streuli CH, Schmidhauser C, Kokrin M, Bissel MJ, Derynck R. Extracellular matrix regulates expression of the TGF-betal gene. J Cell Biol 1993, 120, 253-260.
60. 60. Nilsen-Hamilton M. Transforming growth factor-beta and its actions on cellular growth and differentiation. Curr Top Dev Biol 1990, 24, 95-136.
61. 61. Edwards DR, Murphy G, Reynolds JJ, Whitman SE, Docherty AJP, Angel P, Heath JK. Transforming growth factor beta modulates the expression of collagenases and metallproteinase inhibitor. EMBO J 1987, 6, 1899-1914.
62. 62. Border WA, Ruoslahti E. Transforming growth factor β: The dark side of tissue repair. J Clin Invest 1992, 90, 1-7.
63. 63. Ruoslahti E, Yamaguchi Y. Proteoglycans as modulators of growth factor activities. Cell 1992, 64, 869-876.
64. 64. Shah M, Foreman DM, Ferguson MW. Control of scarring in adult wounds by neutralizing antibody to transforming growth factor beta. Lancet 1992, 339, 213-214.
65. 65. Olson EN, Sternberg E, Shan Hu J, Spizz G, Wilcox C. Regulation of myogenic differentiation by type β transforming growth factor. J Cell Biol 1986, 103, 1799-1805.
66. 66. Allen RE, Boxhorn LA. Regulation of skeletal muscle satellite cell proliferation by transforming growth factor β, insulin-like growth factor-I and fibroblast growth factor. J Cell Physiol 1989, 138, 311-315.
67. 67. Dodson MV, Allen RE, Hossner KL. Ovine somatomedin, multiplication-stimulating activity and insulin promote skeletal muscle satellite cell proliferation in vitro. Endocrinology 1985, 117, 2357-2363.
68. 68. Ewton DZ, Florini JR. Effects of the somatomedines and insulin on myoblast differentiation in vitro. Devl Biol 1981, 86, 31-39.
69. 69. Ewton DA, Florini JR. Relative effects of the somatomedins, multiplication-stimulating activity, and growth hormone on myoblast and myotubes in culture. Endocrinology 1980, 106, 577-583.
70. 70. Monier S, Le Marchand-Brustel Y. Effects of insulin and IGF-I on RNA synthesis in isolated soleus muscle. Mol Cell Endocrinol. 1984, 37, 109-114.
71. 71. Jennische E, Skottner A, Hansson HA. Satellite cells express the trophic factor IGF-I in regenerating skeletal muscle. Acta Physiol Scand 1987, 129, 9-15.
72. 72. Florini JR, Margri KA, Ewton DZ, James PL, Grindstaff K, Rotwein PS. "Spontaneous" differentiation of skeletal myoblasts is dependent upon autocrine secretion of insulin-like growth factor-II. J Biol Chem 1991, 266, 15917-15923.
73. 73. Tollefsen SE, Sadow JL, Rotwein PS. Coordinate expression of insulin-like growth factor-II and its receptor during muscle differentiation. Proc Natl Acad Sci USA 1989, 86, 1543-1547.
74. 74. Tollefsen SE, Lajara R, McCusker RH, Clemmons DR, Rotwein P. Insulin-like growth factor (IGF) in muscle development. J Biol Chem 1989, 264, 13810-13817.
75. 75. Livingston N, Pollare T, Lithell H, Arner P. Characterization of insulin-like growth factor-I receptor in skeletal muscles of normal and insulin resistant subjects. Diabetologia 1988, 31, 871-877.
76. 76. Rosenthal SM, Brunetti A, Brown EJ, Manuela PW, Goldfine JD. Regulation of insulin-like growth factor (IGF) I receptor expression during muscle cell differentiation. Potential autocrine role of IGF-II. J Clin Invest 1991, 87, 1212-1219.
77. 77. Ewton DZ, Roof SL, Magri KA, McWade FJ, Florini JR. IGF-II is more active than IGF-I in stimulating L6A1 myogenesis: greater mitogenic actions of IGF-I delay differentiation. J Cell Physiol 1994, 16, 277-284.
78. 78. Baxter RC, Martin LJ. Binding proteins for the insulin-like growth factors: structure, regulation and function. Prog Growth Factor Res 1989, 1, 49-68.
79. 79. Rauvala H. An 18-kd heparin binding protein of developing brain that is distinct from fibroblast growth factors. EMBO J 1989, 8, 2933-2941.
80. 80. Li Y-S, Milner PG, Chauhan AK, Watson MA, Hoffman RM, Kodner CM, Milbrandt J, Deuel TF. Cloning and expression of a developmentally regulated protein that induces mitogenic and neurite outgrowth activity. Science 1990, 250, 26011-26016.
81. 81. Laaroubi K, Delbé J, Vacherot F, Desgranges P, Tardieu M, Jaye M, Barritault D, Courty J. Mitogenic and in vitro angiogenic activity of human recombinant heparin affin regulatory peptide. Growth Factors 1994, 10, 89-98.
82. 82. Laaroubi K, Vacherot F, Delbé J, Caruelle D, Barritault D, Courty J. Biochemical and mitogenic properties of the heparin binding growth factor HARP. Prog Growth Factor Res 1995, 6, 25-34.
83. 83. Delbé J, Vacherot F, Laaroubi K, Barritault D, Courty J. Effect of heparin on bovine epithelial lens cell proliferation induced by heparin affin regulatory peptide. J Cell Physiol 1995, 164, 47-54.
84. 84. Courty J, Dauchel MC, Caruelle D, Perderiset M, Barritault D. Mitogenic properties of a new endothelial cell growth factor related to pleiotrophin. Biochem Biophys Res Commun 1991, 180, 145-151.
85. 85. Kadomatsu K, Tomomura M, Muramatsu T. cDNA cloning and sequencing of a new gene intensely expressed in early differentiation stages of embryonal carcinoma cells and in mid-gestation period of mouse embryogenesis. Biochem Biophys Res Commun 1988, 151, 1312-1318.
86. 86. Li YS, Gurrieri M, Deuel TF. Pleiotrophin gene expression is highly restricted and is regulated by platelet-derived growth factor. Biochem Biophys Res Commun 1992, 184, 427-432.
87. 87. Mitsiadis TA, Salmivirta M, Muramatsu T, Muramatsu H, Rauvala H, Lehtonen E, Jalkanan M, Thesleff I. Expression of the heparin-binding cytokines, midkine (MK) and HB-GAM (pleiotrophin) is associated with epithelial-mesenchymal interactions during fetal development and organogenesis. Development 1995, 121, 37-51.
88. 88. Muramatsu T. Midkine (MK), the product of a retinoic-acid responsive gene, and pelitrophin constitute a new protein family regulating growth and differentiation. Int J Devl Biol 1993, 37, 183-188.
89. 89. Merenmies J. Cell density-dependent expression of heparin-binding growth-associated molecule (HB-GAM, p18) and its down regulation by fibroblast growth factors. FEBS Lett 1992, 307, 297-300.
90. 90. Peng HB, Ali AA, Dai Z, Daggett DF, Raulo E, Rauvala H. The role of heparin-binding growth-associated molecule (HB-GAM) in the postsynaptic induction in cultured muscle cells. J Neurosci 1995, 15, 3027-3038.
91. 91. Rauvala H, Vanhala A, Castren E, Nolo R, Raulo E, Merenmies J, Panula P. Expression of HB-GAM (heparin-binding growth-associated molecule) in the pathways of developing axonal processes in vivo and neurite outgrowth in vitro induced by HB-GAM. Devl Brain Res 1994, 79, 157-176.
92. 92. Gough NM, Gearing DP, King JA, Willson TA, Hilton DJ, Nicola NA, Metcalf D. Molecular cloning and expression of the human homologue of the murine gene encoding myeloid leukemia-inhibitory factor. Proc Natl Acad Sci USA 1988, 85, 2623-2627.
93. 93. Rathjen PD, Nichols J, Toth S, Edwards DR, Heath JK, Smith AG. Developmentally programmed induction of differentiation inhibiting activity and the control of stem cell populations. Genes Devl 1990, 4, 2308-2318.
94. 94. Austin L, Burgess A. Stimulation of myoblast proliferation in culture by leukemia inhibitory factor and other cytokines. J Neurol Sci 1991, 101, 193-197.
95. 95. Austin L, Bower J, Kurek J, Vakakis N. Effects of leukemia inhibitory factor and other cytokines on murine and human myoblast proliferation. J Neurol Sci 1992, 112, 185-191.
96. 96. Bower J, Vakakis N, Nicola NA, Austin L. Specific binding of leukemia inhibitory factor to murine myoblasts in culture. J Cell Physiol 1995, 164, 93-98.
97. 97. Barnard W, Bower J, Brown M, Murphy M, Austin L. Leukemia inhibitory factor (LIF) infusion stimulates skeletal muscle regeneration after injury: Injured muscle expresses LIF mRNA. J Neurol Sci 1994, 123, 108-113.
98. 98. Rizzino A, Kaziakoff P, Raff E, Kuzynski C, Nebelsick J. Regulatory effects of cell density on the binding of transforming growth factor β, epidermal growth factor, platelet-derived growth factor and fibroblast growth factor. Cancer Res 1988, 48, 4266-4271.
99. 99. Richardson PM. Ciliary neurotrophic factor: a review. Pharmacol Ther 1994, 63, 187-198.
100. 100. Helgren ME, Squinto SP, Davis HL, Parry DJ, Boulton TG, Hech CS, Zhu Y, Yancopoulos GD, Lindsay RM, DiStefano PS. Trophic effect of ciliary neurotrophic factor on denervated skeletal muscle. Cell 1994, 76, 493-504.
101. 101. Piquet-Pellorce C, Grey L, Mereau A, Heath JK. Are LIF and related cytokines functionally equivalent? Exp Cell Res 1994, 213, 340-347.
102. 102. Sendtner M, Carroll P, Holtmann B, Hughes RA, Thoenen H. Ciliary neurotrophic factor. J Neurobiol 1994, 25, 1436-1453.
103. 103. English AW, Schwartz G. Both basic fibroblast growth factor and ciliary neurotrophic factor promote the retention of polyneuronal innervation of developing skeletal muscle fibers. Devl Biol 1995, 1698, 57-64.
104. 104. Borycki AG, Smadja F, Stanley R, Leibovitch SA. Colony-stimulating factor 1 (CSF-1) is involved in an autocrine growth control of rat myogenic cells. Exp Cell Res 1994, 218, 213-222.
105. 105. Allen RE, Shechan SM, Taylor RG, Kendall TG, Rice GM. Hepatocyte growth facotr activates quiescent skeletal muscle satellite cells in vitro. J Cell Physiol 1995, 165, 307-312.
106. 106. Matsumoto K, Okazaki H, Nakamura T. Novel function of prostaglandins as inducers of gene expression of HGF and putative mediators of tissue regeneration. J Biochem (Tokyo) 1995, 117, 458-464.
107. 107. Bassaglia Y, Gautron J. Fast and slow rat muscles degenerate and regenerate differently after whole muscle crush injury. J Muscle Res Cell Motil 1995, 16, 420-429.
108. 108. Gautron J, Kedzia C, Husmann I, Barritault D. Accélération de la régénération d'un muscle squelettique de rat adulte par des dérivés de dextranes. CR Acad Sci Paris 1995, 318, 671-676.