FGF6 in myogenesis

Biochimica et Biophysica Acta - Molecular Cell Research

Volumn 1763, Issue 8, 2006, Pages 773-778

  Armand, Anne Sophie ^a   Laziz, Iman ^b   Chanoine, Christophe ^b  

^a ROYAL NETHERLANDS ACADEMY OF ARTS AND SCIENCES   (Netherlands)

^b CNRS   (France)

Author keywords

Development; FGF6; Growth factor; Muscle regeneration; Myogenesis

Indexed keywords

AMINO ACID; FIBROBLAST GROWTH FACTOR; FIBROBLAST GROWTH FACTOR 6; GENE PRODUCT; MITOGEN ACTIVATED PROTEIN KINASE 1; MITOGEN ACTIVATED PROTEIN KINASE 3; SOMATOMEDIN B; UNCLASSIFIED DRUG;

CELL DIFFERENTIATION; CELL MIGRATION; CELL PROLIFERATION; FIBROBLAST GROWTH FACTOR 6 GENE; GENE; GENE EXPRESSION; GENE STRUCTURE; KNOCKOUT GENE; MOUSE STRAIN; MUSCLE DEVELOPMENT; MUSCLE HYPERTROPHY; MUSCLE REGENERATION; MYOBLAST; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN FUNCTION; REVIEW; SKELETAL MUSCLE; STEM CELL;

ANIMALS; CELL DIFFERENTIATION; FIBROBLAST GROWTH FACTOR 6; GENE EXPRESSION; HYPERTROPHY; MICE; MICE, KNOCKOUT; MUSCLE DEVELOPMENT; MUSCLES; PHENOTYPE; PROTO-ONCOGENE PROTEINS; RECEPTORS, FIBROBLAST GROWTH FACTOR; REGENERATION; SIGNAL TRANSDUCTION; STEM CELLS;

EID: 33746986505     PISSN: 01674889     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbamcr.2006.06.005     Document Type: Review

References (60)

1. Ornitz D.M., and Itoh N. Fibroblast growth factors. Genome Biol. 2 (2001) 3005-3012
2. Szebenyi G., and Fallon J.F. Fibroblast growth factors as multifunctional signaling factors. Int. Rev. Cytol. 185 (1999) 45-106
3. deLapeyriere O., Ollendorff V., Planche J., Ott M.O., Pizette S., Coulier F., and Birnbaum D. Expression of the Fgf6 gene is restricted to developing skeletal muscle in the mouse embryo. Development 118 (1993) 601-611
4. Han J.K., and Martin G.R. Embryonic expression of FGF6 is restricted to the skeletal muscle lineage. Dev. Biol. 158 (1993) 549-554
5. Grass S., Arnold H.H., and Braun T. Alterations in somite patterning of Myf-5-deficient mice: a possible role for FGF-4 and FGF6. Development 122 (1996) 141-150
6. Pizette S., Coulier F., Birnbaum D., and deLapeyriere O. FGF6 modulates the expression of fibroblast growth factor receptors and myogenic genes in muscle cells. Exp. Cell Res. 224 (1996) 143-151
7. Floss T., Arnold H.H., and Braun T. A role for FGF6 in skeletal muscle regeneration. Genes Dev. 11 (1997) 2040-2051
8. Fiore F., Sebille A., and Birnbaum D. Skeletal muscle regeneration is not impaired in Fgf6-/- mutant mice. Biochem. Biophys. Res. Commun. 272 (2000) 138-143
9. Fiore F., Planche J., Gibier P., Sebille A., de Lapeyriere O., and Birnbaum D. Apparent normal phenotype of Fgf6-/- mice. Int. J. Dev. Biol. 41 (1997) 639-642
10. Armand A.S., Pariset C., Laziz I., Launay T., Fiore F., Della Gaspera B., Birnbaum D., Charbonnier F., and Chanoine C. FGF6 regulates muscle differentiation through a calcineurin-dependent pathway in regenerating soleus of adult mice. J. Cell. Physiol. 204 (2005) 297-308
11. de Lapeyriere O., Rosnet O., Benharroch D., Raybaud F., Marchetto S., Planche J., Galland F., Mattei M.G., Copeland N.G., Jenkins N.A., et al. Structure, chromosome mapping and expression of the murine Fgf-6 gene. Oncogene 5 (1990) 823-831
12. Katoh Y., and Katoh M. Comparative genomics on mammalian Fgf6-Fgf23 locus. Int. J. Mol. Med. 16 (2005) 355-358
13. Coulier F., Pizette S., Ollendorff V., deLapeyriere O., and Birnbaum D. The human and mouse fibroblast growth factor 6 (FGF6) genes and their products: possible implication in muscle development. Prog. Growth Factor Res. 5 (1994) 1-14
14. Rescan P.Y. Identification of a fibroblast growth factor 6 (FGF6) gene in a non-mammalian vertebrate: continuous expression of FGF6 accompanies muscle fiber hyperplasia. Biochim. Biophys. Acta 1443 (1998) 305-314
15. Terova G., Bernardini G., Binelli G., Gornati R., and Saroglia M. cDNA encoding sequences for myostatin and FGF6 in sea bass (Dicentrarchus labrax, L.) and the effect of fasting and refeeding on their abundance levels. Domest. Anim. Endocrinol. 30 (2006) 304-319
16. Sakuma K., Watanabe K., Sano M., Uramoto I., and Totsuka T. Differential adaptation of growth and differentiation factor 8/myostatin, fibroblast growth factor 6 and leukemia inhibitory factor in overloaded, regenerating and denervated rat muscles. Biochim. Biophys. Acta 1497 (2000) 77-88
17. Armand A.S., Launay T., Pariset C., Della Gaspera B., Charbonnier F., and Chanoine C. Injection of FGF6 accelerates regeneration of the soleus muscle in adult mice. Biochim. Biophys. Acta 1642 (2003) 97-105
18. Zhao P., and Hoffman E.P. Embryonic myogenesis pathways in muscle regeneration. Dev. Dyn. 229 (2004) 380-392
19. Garrett K.L., and Anderson J.E. Colocalization of bFGF and the myogenic regulatory gene myogenin in dystrophic mdx muscle precursors and young myotubes in vivo. Dev. Biol. 169 (1995) 596-608
20. Hebert J.M., Basilico C., Goldfarb M., Haub O., and Martin G.R. Isolation of cDNAs encoding four mouse FGF family members and characterization of their expression patterns during embryogenesis. Dev. Biol. 138 (1990) 454-463
21. Mason I.J., Fuller-Pace F., Smith R., and Dickson C. FGF-7 (keratinocyte growth factor) expression during mouse development suggests roles in myogenesis, forebrain regionalisation and epithelial-mesenchymal interactions. Mech. Dev. 45 (1994) 15-30
22. Sheehan S.M., and Allen R.E. Skeletal muscle satellite cell proliferation in response to members of the fibroblast growth factor family and hepatocyte growth factor. J. Cell. Physiol. 181 (1999) 499-506
23. Kästner S., Elias M.C., Rivera A.J., and Yablonka-Reuveni Z. Gene expression patterns of the fibroblast growth factors and their receptors during myogenesis of rat satellite cells. J. Histochem. Cytochem. 48 (2000) 1079-1096
24. Israeli D., Benchaouir R., Ziaei S., Rameau P., Gruszczynski C., Peltekian E., Danos O., and Garcia L. FGF6 mediated expansion of a resident subset of cells with SP phenotype in the C2C12 myogenic line. J. Cell Physiol. 201 (2004) 409-419
25. Johnson D.E., and Williams L.T. Structural and functional diversity in the FGF receptor multigene family. Adv. Cancer Res. 60 (1993) 1-41
26. Vainikka S., Partanen J., Bellosta P., Coulier F., Birnbaum D., Basilico C., Jaye M., and Alitalo K. Fibroblast growth factor receptor-4 shows novel features in genomic structure, ligand binding and signal transduction. EMBO J. 11 (1992) 4273-4280
27. Ornitz D.M., Xu J., Colvin J.S., McEwen D.G., MacArthur C.A., Coulier F., Gao G., and Goldfarb M. Receptor specificity of the fibroblast growth factor family. J. Biol. Chem. 271 (1996) 15292-15297
28. Deng C.X., Wynshaw-Boris A., Shen M.M., Daugherty C., Ornitz D.M., and Leder P. Murine FGFR-1 is required for early postimplantation growth and axial organization. Genes Dev. 8 (1994) 3045-3057
29. Deng C., Bedford M., Li C., Xu X., Yang X., Dunmore J., and Leder P. Fibroblast growth factor receptor-1 (FGFR-1) is essential for normal neural tube and limb development. Dev. Biol. 185 (1997) 42-54
30. Yamaguchi T.P., Harpal K., Henkemeyer M., and Rossant J. FGFR-1 is required for embryonic growth and mesodermal patterning during mouse gastrulation. Genes Dev. 8 (1994) 3032-3044
31. Weinstein M., Xu X., Ohyama K., and Deng C.X. FGFR-3 and FGFR-4 function cooperatively to direct alveogenesis in the murine lung. Development 125 (1998) 3615-3623
32. Wang Z.Q., Fung M.R., Barlow D.P., and Wagner E.F. Regulation of embryonic growth and lysosomal targeting by the imprinted Igf2/Mpr gene. Nature 372 (1994) 464-467
33. Vainikk S., Joukov V., Wennstrom S., Bergman M., Pelicci P.G., and Alitalo K. Signal transduction by fibroblast growth factor receptor-4 (FGFR-4), comparison with FGFR-1. J. Biol. Chem. 269 (1994) 18320-18326
34. Jones N.C., Fedorov Y.V., Rosenthal R.S., and Olwin B.B. ERK1/2 is required for myoblast proliferation but is dispensable for muscle gene expression and cell fusion. J. Cell. Physiol. 186 (2001) 104-115
35. Marics I., Padilla F., Guillemot J.F., Scaal M., and Marcelle C. FGFR4 signaling is a necessary step in limb muscle differentiation. Development 129 (2002) 4559-4569
36. Neuhaus P., Oustanina S., Loch T., Kruger M., Bober E., Dono R., Zeller R., and Braun T. Reduced mobility of fibroblast growth factor (FGF)-deficient myoblasts might contribute to dystrophic changes in the musculature of FGF2/FGF6/mdx triple-mutant mice. Mol. Cell Biol. 23 (2003) 6037-6048
37. Doetschman T. Interpretation of phenotype in genetically engineered mice. Lab. Anim. Sci. 49 (1999) 137-143
38. Valenti P., Cozzio A., Nishida N., Wolfer D.P., Sakaguchi S., and Lipp H.P. Similar target, different effects: late-onset ataxia and spatial learning in prion protein-deficient mouse lines. Neurogenetics 3 (2001) 173-184
39. Mansour S.L., Goddard J.M., and Capecchi M.R. Mice homozygous for a targeted disruption of the proto-oncogene int-2 have developmental defects in the tail and inner ear. Development 117 (1993) 13-28
40. Lefaucheur J.P., and Sebille A. Basic fibroblast factor promotes in vivo muscle regeneration in murine muscular dystrophy. Neurosci. Lett. 202 (1995) 121-124
41. Menetrey J., Kasemkijwattana C., Day C.S., Bosch P., Vogt M., Fu F.H., Moreland M.S., and Huard J. Growth factors improve muscle healing in vivo. J. Bone Joint Surg. Br. 82 (2000) 131-137
42. Doukas J., Blease K., Craig D., Ma C., Chandler L.A., Sosnowski B.A., and Pierce G.F. Delivery of FGF genes to wound repair cells enhances arteriogenesis and myogenesis in skeletal muscle. Mol. Ther. 5 (2002) 517-527
43. Webb S.E., Lee K.K., Tang M.K., and Ede D.A. Fibroblast growth factors 2 and 4 stimulate migration of mouse embryonic limb myogenic cells. Dev. Dyn. 209 (1997) 206-216
44. Itoh N., Mima T., and Mikawa T. Loss of fibroblast growth factor receptors is necessary for terminal differentiation of embryonic limb muscle. Development 122 (1996) 291-300
45. Bunting K.D. ABC transporters as phenotypic markers and functional regulators of stem cells. Stem. Cells 20 (2002) 11-20
46. Decraene C., Benchaouir R., Dillies M.A., Israeli D., Bortoli S., Rochon C., Rameau P., Pitaval A., Tronik-Le Roux D., Danos O., Gidrol X., Garcia L., and Pietu G. Global transcriptional characterization of SP and MP cells from the myogenic C2C12 cell line: effect of FGF6. Physiol. Genomics 23 (2005) 132-149
47. Friday B.B., Horsley V., and Pavlath G.K. Calcineurin activity is required for the initiation of skeletal muscle differentiation. J. Cell Biol. 149 (2000) 657-666
48. Chin E.R., Olson E.N., Richardson J.A., Yang Q., Humphries C., Shelton J.M., Wu H., Zhu W., Bassel-Duby R., and Williams R.S. A calcineurin-dependent transcriptional pathway controls skeletal muscle fiber type. Genes Dev. 12 (1998) 2499-2509
49. Naya F.J., Mercer B., Shelton J., Richardson J.A., Williams R.S., and Olson E.N. Stimulation of slow skeletal muscle fiber gene expression by calcineurin in vivo. J. Biol. Chem. 275 (2000) 4545-4548
50. McCullagh K.J., Calabria E., Pallafacchina G., Ciciliot S., Serrano A.L., Argentini C., Kalhovde J.M., Lomo T., and Schiaffino S. NFAT is a nerve activity sensor in skeletal muscle and controls activity-dependent myosin switching. Proc. Natl. Acad. Sci. U. S. A. 101 (2004) 10590-10595
51. Armand AS., Lecolle S., Launay T., Pariset C., Fiore F., Della Gaspera B., Birnbaum D., Chanoine C., and Charbonnier F. IGF-II is up-regulated and myofibres are hypertrophied in regenerating soleus of mice lacking FGF6. Exp. Cell Res. 297 (2004) 27-38
52. Florini J.R., Ewton D.Z., and Coolican S.A. Growth hormone and the insulin-like growth factor system in myogenesis. Endocr. Rev. 17 (1996) 481-517
53. Seale P., and Rudnicki M.A. A new look at the origin, function, and "stem-cell" status of muscle satellite cells. Dev. Biol. 218 (2000) 115-124
54. De Meyts P., Wallach B., Christoffersen C.T., Urso B., Gronskov K., Latus L.J., Yakushiji F., Ilondo M.M., and Shymko R.M. The insulin-like growth factor-I receptor. Structure, ligand-binding mechanism and signal transduction. Horm. Res. 42 (1994) 152-169
55. Kornfeld S. Structure and function of the mannose 6-phosphate/insulinlike growth factor II receptors. Annu. Rev. Biochem. 61 (1992) 307-330
56. Wang Z.Q., Fung M.R., Barlow D.P., and Wagner E.F. Regulation of embryonic growth and lysosomal targeting by the imprinted Igf2/Mpr gene. Nature 372 (1994) 464-467
57. Huang C.Y., Hao L.Y., and Buetow D.E. Insulin-like growth factor-induced hypertrophy of cultured adult rat cardiomyocytes is L-type calcium-channel-dependent. Mol. Cell. Biochem. 231 (2002) 51-59
58. Ikezu T., Okamoto T., Giambarella U., Yokota T., and Nishimoto I. In vivo coupling of insulin-like growth factor II/mannose 6-phosphate receptor to heteromeric G proteins. Distinct roles of cytoplasmic domains and signalsequestration by the receptor. J. Biol. Chem. 270 (1995) 29224-29228
59. McPherron A.C., Lawler A.M., and Lee S.J. Regulation of skeletal muscle mass in mice by a new TGF-beta superfamily member. Nature 387 (1997) 83-90
60. Kocamis H., Gahr S.A., Batelli L., Hubbs A.F., and Killefer J. IGF-I, IGF-II, and IGF-receptor-1 transcript and IGF-II protein expression in myostatin knockout mice tissues. Muscle Nerve 26 (2002) 55-63