FGF receptor availability regulates skeletal myogenesis

Experimental Cell Research

Volumn 250, Issue 1, 1999, Pages 10-21

  Scata, Kimberly A ^a   Bernard, David W ^a   Fox, Jonathan ^a   Swain, Judith L ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

FGF; FGF receptor; Myogenesis; Signal transduction; Skeletal muscle

Indexed keywords

CELL SURFACE RECEPTOR; FIBROBLAST GROWTH FACTOR; FIBROBLAST GROWTH FACTOR RECEPTOR; TYROSINE KINASE RECEPTOR;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; AUTOCRINE EFFECT; CELL DIFFERENTIATION; CELL PROLIFERATION; EMBRYO DEVELOPMENT; LIGAND BINDING; MOUSE; MUSCLE CELL; MUSCLE DEVELOPMENT; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; REGULATORY MECHANISM; SIGNAL TRANSDUCTION; SKELETAL MUSCLE;

EID: 0033542791     PISSN: 00144827     EISSN: None     Source Type: Journal    
DOI: 10.1006/excr.1999.4506     Document Type: Article

References (39)

1. Emerson C. P. Jr. Embryonic signals for skeletal myogenesis: Arriving at the beginning. Curr. Opin. Cell Biol. 5:1993;1057-1064.
2. Olson E. N. Signal transduction pathways that regulate skeletal muscle gene expression. Mol. Endocrinol. 7:1993;1369-1378.
3. Clegg C. H., Linkhart T. A., Olwin B. B., Hauschka S. D. Growth factor control of skeletal muscle differentiation: Commitment to terminal differentiation occurs in G1 phase and is repressed by fibroblast growth factor. J. Cell Biol. 105:1987;949-956.
4. Spizz G., Hu J. S., Olson E. N. Inhibition of myogenic differentiation by fibroblast growth factor or type beta transforming growth factor does not require persistent c-myc expression. Dev. Biol. 123:1987;500-507.
5. Groux-Muscatelli B., Bassaglia Y., Barritault D., Caruelle J. P., Gautron J. Proliferating satellite cells express acidic fibroblast growth factor during in vitro myogenesis. Dev. Biol. 142:1990;380-385.
6. Moore J. W., Dionne C., Jaye M., Swain J. L. The mRNAs encoding acidic FGF, basic FGF and FGF receptor are coordinately downregulated during myogenic differentiation. Development. 111:1991;741-748.
7. Fox J. C., Hsu A. Y., Swain J. L. Myogenic differentiation triggered by antisense acidic fibroblast growth factor RNA. Mol. Cell. Biol. 14:1994;4244-4250.
8. Soulet L., Chevet E., Lemaitre G., Blanquaert F., Meddahi A., Barritault D. FGFs and their receptors, in vitro and in vivo studies: New FGF receptor in the brain, FGF-1 in muscle, and the use of functional analogues of low-affinity heparin-binding growth factor receptors in tissue repair. Mol. Reprod. Dev. 39:1994;49-54.
9. Fantl W. J., Johnson D. E., Williams L. T. Signalling by receptor tyrosine kinases. Annu. Rev. Biochem. 62:1993;453-481.
10. Jaye M., Schlessinger J., Dionne C. A. Fibroblast growth factor receptor tyrosine kinases: Molecular analysis and signal transduction. Biochim. Biophys. Acta. 1135:1992;185-199.
11. Johnson D. E., Williams L. T. Structural and functional diversity in the FGF receptor multigene family. Adv. Cancer Res. 60:1993;1-41.
12. Partanen J., Makela T. P., Eerola E., Korhonen J., Hirvonen H., Claesson W. L., Alitalo K. FGFR-4, a novel acidic fibroblast growth factor receptor with a distinct expression pattern. EMBO J. 10:1991;1347-1354.
13. Stark K. L., McMahon J. A., McMahon A. P. FGFR-4, a new member of the fibroblast growth factor receptor family, expressed in the definitive endoderm and skeletal muscle lineages of the mouse. Development. 113:1991;641-651.
14. Templeton T. J., Hauschka S. D. FGF-mediated aspects of skeletal muscle growth and differentiation are controlled by a high affinity receptor, FGFR1. Dev. Biol. 154:1992;169-181.
15. Bellot F., Crumley G., Kaplow J. M., Schlessinger J., Jaye M., Dionne C. A. Ligand-induced transphosphorylation between different FGF receptors. EMBO J. 10:1991;2849-2854.
16. Ueno H., Gunn M., Dell K., Tseng A. J., Williams L. T. A truncated form of fibroblast growth factor receptor 1 inhibits signal transduction by multiple types of fibroblast growth factor receptor. J. Biol. Chem. 267:1992;1470-1476.
17. Amaya E., Musci T. J., Kirschner M. W. Expression of a dominant negative mutant of the FGF receptor disrupts mesoderm formation in Xenopus embryos. Cell. 66:1991;257-270.
18. Amaya E., Stein P. A., Musci T. J., Kirschner M. W. FGF signalling in the early specification of mesoderm in Xenopus. Development. 118:1993;477-487.
19. Shi E., Kan M., Xu J., Wang F., Hou J., McKeehan W. L. Control of fibroblast growth factor receptor kinase signal transduction by heterodimerization of combinatorial splice variants. Mol. Cell. Biol. 13:1993;3907-3918.
20. Peters K., Werner S., Liao X., Wert S., Whitsett J., Williams L. T. Targeted expression of a dominant negative FGF receptor blocks branching morphogenesis and epithelial differentiation of the mouse lung. EMBO J. 13:1994;3296-3301.
21. Werner S., Weinberg W., Liao X., Peters K. G., Blessing M., Yuspa S. H., Weiner R. L., Williams L. T. Targeted expression of a dominant-negative FGF receptor mutant in the epidermis of transgenic mice reveals a role of FGF in keratinocyte organization and differentiation. EMBO J. 12:1993;2635-2643.
22. Mima T., Ueno H., Fischman D. A., Williams L. T., Mikawa T. Fibroblast growth factor receptor is required for in vivo cardiac myocyte proliferation at early embryonic stages of heart development. Proc. Natl. Acad. Sci. USA. 92:1995;467-471.
23. Kunkel T. A. Rapid and efficient site-specific mutagenesis without phenotypic selection. Proc. Natl. Acad. Sci. USA. 82:1985;488-492.
24. Takebe Y., Seiki M., Fujisawa J., Hoy P., Yokota K., Arai K., Yoshida M., Arai N. SR alpha promoter: An efficient and versatile mammalian cDNA expression system composed of the simian virus 40 early promoter and the R-U5 segment of human T-cell leukemia virus type 1 long terminal repeat. Mol. Cell. Biol. 8:1988;466-472.
25. Evan G. I., Lewis G. K., Ramsay G., Bishop J. M. Isolation of monoclonal antibodies specific for human c-myc proto-oncogene product. Mol. Cell. Biol. 5:1985;3610-3616.
26. Montarras D., Pinset C., Chelly J., Kahn A., Gros F. Expression of MyoD1 coincides with terminal differentiation in determined but inducible muscle cells. EMBO J. 8:1989;2203-2207.
27. Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162:1987;156-159.
28. Dionne C. A., Modi W. S., Crumley G., O'Brien S. J., Schlessinger J., Jaye M. BEK, a receptor for multiple members of the fibroblast growth factor (FGF) family, maps to human chromosome 10q25.3 - - q26. Cytol. Cell Genet. 60:1992;34-36.
29. Feige J. J., Baird A. Glycosylation of the basic fibroblast growth factor receptor. The contribution of carbohydrate to receptor function. J. Biol. Chem. 263:1988;14023-14029.
30. Johnson D. E., Williams L. T. Structural and functional diversity in the FGF receptor multigene family. Adv. Cancer Res. 60:1993;1-41.
31. Olson E. N., Caldwell K. L., Gordon J. I., Glaser L. Regulation of creatine phosphokinase expression during differentiation of BC3H1 cells. J. Biol. Chem. 258:1983;2644-2652.
32. Spizz G., Roman D., Strauss A., Olson E. N. Serum and fibroblast growth factor inhibit myogenic differentiation through a mechanism dependent on protein synthesis and independent of cell proliferation. J. Biol. Chem. 261:1986;9483-9488.
33. Vainikka S., Joukov V., Wennstrom S., Bergman M., Pelicci P. G., Alitalo K. Signal transduction by fibroblast growth factor receptor-4 (FGFR-4): Comparison with FGFR-1. J. Biol. Chem. 269:1994;18320-18326.
34. Wang J. K., Gao G., Goldfarb M. Fibroblast growth factor receptors have different signaling and mitogenic potentials. Mol. Cell. Biol. 14:1994;181-188.
35. Itoh N., Mima T., Mikawa T. Loss of fibroblast growth factor receptors is necessary to terminal differentiation of embryonic limb muscle. Development. 122:1996;291-300.
36. Zhou M., Sutliff R. L., Paul R. J., Lorenz J. N., Hoying J. B., Haudenschild C. C., Yin M., Coffin J. D., Kong L., Kranias E. G., Luo W., Boivin G. P., Duffy J. J., Pawlowski S. A., Doetschman T. Fibroblast growth factor 2 control of vascular tone. Nature Med. 4:1998;201-207.
37. Lindsell C. E., Shawber C. J., Boulter J., Weinmaster G. Jagged: A mammalian ligand activates Notch 1. Cell. 80:1995;909-917.
38. Shawber C., Nofziger D., Hsieh J. J., Lindsell C., Bogler O., Hayward D., Weinmaster G. Notch signaling inhibits muscle cell differentiation through a CBF-1-independent pathway. Development. 122:1996;3765-3773.
39. Zimrin A. B., Pepper M. S., McMahon G. A., Nguyen F., Montesano R., Maciag T. An antisense oligonucleotide to the Notch ligand Jagged enhances Fibroblast Growth Factor-induced angiogenesis in vitro. J. Biol. Chem. 271:1996;32499-32502.