Dynamic expression of proteoglycans during chicken skeletal muscle development and maturation

Poultry Science

Volumn 78, Issue 5, 1999, Pages 769-777

  Carrino, David A ^a   Sorrell, J Michael ^a   Caplan, Arnold I ^a  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Chondroitin sulfate; Development; Glycosaminoglycan; Muscle; Proteoglycan

Indexed keywords

GALLUS GALLUS;

PROTEOGLYCAN;

ANIMAL; ARTICLE; BIOSYNTHESIS; CHICKEN; CYTOLOGY; GENE EXPRESSION REGULATION; GROWTH, DEVELOPMENT AND AGING; MEAT; MUSCLE CELL; MUSCLE DEVELOPMENT; SKELETAL MUSCLE;

ANIMALS; CHICKENS; GENE EXPRESSION REGULATION, DEVELOPMENTAL; MEAT; MUSCLE DEVELOPMENT; MUSCLE FIBERS; MUSCLE, SKELETAL; PROTEOGLYCANS;

EID: 0033124220     PISSN: 00325791     EISSN: None     Source Type: Journal    
DOI: 10.1093/ps/78.5.769     Document Type: Article

References (65)

1. Ahrens, P. B., M. Solursh, and S. Meier, 1977. The synthesis and localization of glycosaminoglycans in striated muscle differentiating in cell culture. J. Exp. Zool. 202:375-388.
2. Angello, J. C., and S. D. Hauschka, 1979. Hyaluronic acid synthesis and turnover by myotubes in culture. Dev. Biol. 73:322-337.
3. Binette, F., J. Cravens, B. Kahoussi, D. R. Haudenschild, and P. F. Goetinck, 1994. Link protein is ubiquitously expressed in non-cartilaginous tissues where it enhances and stabilizes the interactions of proteoglycans with hyaluronic acid. J. Biol. Chem. 269:19116-19122.
4. Bober, E., T. Franz, H.-H. Arnold, P. Gruss, and P. Tremblay, 1994. Pax-3 is required for the development of limb muscles: a possible role for the migration of dermomyotomal muscle progenitor cells. Development 120: 603-612.
5. Bode-Lesniewska, B., M. T. Dours-Zimmermann, B. F. Odermatt, J. Briner, P. U. Heitz, and D. R. Zimmermann, 1996. Distribution of the large aggregating proteoglycan versican in adult human tissues. J. Histochem. Cytochem. 44: 303-312.
6. Bourin, M.-C., and U. Lindahl, 1993. Glycosaminoglycans and the regulation of blood coagulation. Biochem. J. 289: 313-330.
7. Caplan, A. I., 1976. A simplified procedure for preparing myogenic cells for culture. J. Embryol. Exp. Morphol. 36: 175-181.
8. Caplan, A. I., E. Zwilling, and N. O. Kaplan, 1968. 3-Acetylpyridine: effects in vitro related to teratogenic activity in chicken embryos. Science 160:1009-1010.
9. 35S-labeled proteoglycans on polyacrylamide-agarose composite gels and their visualization by fluorography. Anal. Biochem. 156:38-44.
10. Carrino, D. A., 1998. Dynamic expression of proteoglycans during skeletal muscle development. Basic Appl. Myol. 8: 95-106.
11. Carrino, D. A., and A. I. Caplan, 1982. Isolation and preliminary characterization of proteoglycans synthesized by skeletal muscle. J. Biol. Chem. 257:14145-14154.
12. Carrino, D. A., and A. I. Caplan, 1984. Isolation and partial characterization of high-buoyant-density proteoglycans synthesized in ovo by embryonic chick skeletal muscle and heart. J. Biol. Chem. 259:12419-12430.
13. Carrino, D. A., and A. I. Caplan, 1989. Structural characterization of chick embryonic skeletal muscle chondroitin sulfate proteoglycan. Conn. Tissue Res. 19:35-50.
14. Carrino, D. A., J. E. Dennis, R. F. Drushel, S. E. Haynesworth, and A. I. Caplan, 1994. Identity of the core proteins of the large chondroitin sulfate proteoglycans synthesized by skeletal muscle and prechondrogenic mesenchyme. Biochem. J. 298:51-60.
15. Carrino, D. A., U. Oron, D. G. Pechak, and A. I. Caplan, 1988. Reinitiation of chondroitin sulfate proteoglycan synthesis in regenerating skeletal muscle. Development 103:641-656.
16. Casu, B., 1985. Structure and biological activity of heparin. Adv. Carbohydrate Chem. Biochem. 43:51-134.
17. Chalepakis, G., A. Stoykova, J. Wijnholds, P. Tremblay, and P. Gruss, 1993. Pax: gene regulators in the developing nervous system. J. Neurobiol. 24:1367-1384.
18. Danielson, K. G., H. Baribault, D. F. Holmes, H. Graham, K. E. Kadler, and R. V. Iozzo, 1997. Targeted disruption of decorin leads to abnormal collagen fibril morphology and skin fragility. J. Cell Biol. 136:729-743.
19. Drushel, R. F., and A. I. Caplan, 1991. Three-dimensional reconstruction and cross-sectional anatomy of the thigh musculature of the developing chick embryo (Gallus gallus). J. Morphol. 208:293-309.
20. Fannon, M., and M. A. Nugent, 1996. Basic fibroblast growth factor binds its receptors, is internalized, and stimulates DNA synthesis in Balb/c3T3 cells in the absence of heparan sulfate. J. Biol. Chem. 271:17949-17956.
21. Fernandez, M. S., J. E. Dennis, R. F. Drushel, D. A. Carrino, K. Kimata, M. Yamagata, and A. I. Caplan, 1991. The dynamics of compartmentalization of embryonic muscle by extracellular matrix molecules. Dev. Biol. 147:46-61.
22. Gallagher, J. T., J. E. Turnbull, and M. Lyon, 1992. Patterns of sulfation in heparan sulfate: polymorphism based on a common structural theme. Int. J. Biochem. 24:553-560.
23. Goulding, M., A. Lumsden, and A. J. Paquette, 1994. Regulation of Pax-3 expression in the dermomyotome and its role in muscle development. Development 120:957-971.
24. Henderson, D. J., P. Ybot-Gonzalez, and A. J. Copp, 1997. Over-expression of the chondroitin sulfate proteoglycan versican is associated with defective neural crest migration in the Pax-3 mutant mouse (splotch). Mech. Dev. 69:39-51.
25. Henke, C. A., U. Roongta, D. J. Mickelson, J. R. Knutson, J. B. McCarthy, 1996. CD44-related chondroitin sulfate proteoglycan, a cell surface receptor implicated with tumor cell invasion, mediates endothelial cell migration on fibrinogen and invasion into a fibrin matrix. J. Clin. Invest. 11:2541-2552.
26. Iozzo, R. V., and A. D. Murdoch, 1996. Proteoglycans of the extracellular environment: clues from the gene and protein side offer novel perspectives in molecular diversity and function. FASEB J. 10:598-614.
27. Kieny, M., A. Mauger, A. Chevallier, and M.-P. Pautou, 1988. Origin and development of avian skeletal musculature. Reprod. Nutr. Dev. 28:673-686.
28. Kieny, M., M.-P. Pautou, A. Chevallier, and A. Mauger, 1986. Spatial organization of the developing limb musculature in birds and mammals. Bibl. Anat. 29:65-90.
29. Kimata, K., Y. Oike, K. Tani, T. Shinomura, M. Yamagata, M. Uritani, and S. Suzuki, 1986. A large chondroitin sulfate proteoglycan (PG-M) synthesized before chondrogenesis in the limb bud of chick embryo. J. Biol. Chem. 261: 13517-13525.
30. Laemmli, U. K., 1970. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 680-685.
31. Landolt, R. M., L. Vaughan, K. H. Winterhalter, and D. R. Zimmermann, 1995. Versican is selectively expressed in embryonic tissues that act as barriers to neural crest cell migration and axon outgrowth. Development 121: 2303-2312.
32. Lane, M. C., and M. Solursh, 1988. Dependence of sea urchin primary mesenchyme cell migration on xyloside- and sulfate-sensitive cell surface-associated components. Dev. Biol. 127:78-87.
33. Laurent, C., G. Johnson-Wells, S. Hellström, A. Engström-Laurent, and A. F. Wells, 1991. Localization of hyaluronan in various muscular tissues: a morphological study in the rat. Cell Tissue Res. 263:201-205.
34. Lennon, D. P., D. A. Carrino, M. A. Baber, and A. I. Caplan, 1991. Generation of a monoclonal antibody against avian small dermatan sulfate proteoglycan: immunolocalization and tissue distribution of PG-II (decorin) in embryonic tissues. Matrix 11:412-427.
35. Lohmander, L. S., V. C. Hascall, and A. I. Caplan, 1979. Effects of 4-methyl umbelliferyl-β-D-xylopyranoside on proteoglycan synthesis in chick limb bud mesenchymal cell cultures. J Biol Chem 254:10551-10561.
36. Lyon, M., J. A. Deakin, H. Rahmoune, D. G. Fernig, T. Nakamura, and J. T. Gallagher, 1998. Hepatocyte growth factor/scatter factor binds with high affinity to dermatan sulfate. J. Biol. Chem. 273:271-278.
37. Markwald, R. R., R. B. Runyan, G. T. Kitten, F. M. Funderburg, D. H. Bernanke, and P. R. Brauer, 1984. Use of collagen gel cultures to study heart development: proteoglycan and glycoprotein interactions during the formation of endocardial cushion tissue. Pages 323-350 in: The Role of Extracellular Matrix in Development. R. L. Trelstad, ed. Alan R. Liss, New York, NY.
38. Mason, R. M., J. H. Kimura, and V. C. Hascall, 1982. Biosynthesis of hyaluronic acid in cultures of chondrocytes from the Swarm rat chondrosarcoma. J. Biol. Chem. 257: 2236-2245.
39. Dike, Y., K. Kimata, T. Shinomura, K. Nakazawa, and S. Suzuki, 1980. Structural analysis of chick-embryo cartilage proteoglycan by selective degradation with chondroitin lyases (chondroitinases) and endo-β-D-galactosidase (keratanase). Biochem. J. 191:193-207.
40. Olwin, B. B., and A. Rapraeger, 1992. Repression of myogenic differentiation by aFGF, bFGF, and K-FGF is dependent on cellular heparan sulfate. J. Cell. Biol. 118:631-639.
41. Orkin, R. W., W. Knudson, and B. P. Toole, 1985. Loss of hyaluronate-dependent coat during myoblast fusion. Dev. Biol. 107:527-530.
42. Osdoby, P., and A. I. Caplan, 1976. The possible differentiation of osteogenic elements in vitro from chick limb mesodermal cells. Dev. Biol. 52:283-299.
43. Pacifici, M., and M. Molinaro, 1980. Developmental changes in glycosaminoglycans during skeletal muscle cell differentiation in culture. Exp. Cell Res. 126:143-152.
44. Pechak, D. G., D. A. Carrino, and A. I. Caplan, 1985. Electron microscopic characterization of chick embryonic skeletal muscle proteoglycans. J. Cell Biol. 100:1767-1776.
45. Perris, R., and S. Johanson, 1987. Amphibian neural crest cell migration on purified extracellular matrix components: a chondroitin sulfate proteoglycan inhibits locomotion on fibronectin substrates. J. Cell Biol. 105:2511-2521.
46. Rapraeger, A. C., A. Krufka, and B. B. Olwin, 1991. Requirement of heparan sulfate for bFGF-mediated fibroblast growth and myoblast differentiation. Science 252: 1705-1708.
47. Schlessinger, J., I. Lax, and M. Lemmon, 1995. Regulation of growth factor activation by proteoglycans: what is the role of low affinity receptors? Cell 83:357-360.
48. Shinomura, T., Y. Nishida, K. Ito, and K. Kimata, 1993. cDNA cloning of PG-M, a large chondroitin sulfate proteoglycan expressed during chondrogenesis in chick limb buds: alternative spliced multiforms of PG-M and their relationship to versican. J. Biol. Chem. 268:14461-14469.
49. Sorrell, J. M., D. A. Carrino, M. A. Baber, and A. I. Caplan, 1998. Developmental expression and distribution of versican in human fetal skin. Anat. Embryol. (in press.)
50. Sorrell, J. M., D. A. Carrino, and A. I. Caplan, 1993. Structural domains in chondroitin sulfate identified by antichondroitin sulfate monoclonal antibodies. Immunosequencing of chondroitin sulfates. Matrix 13:351-361.
51. Sorrell, J. M., D. A. Carrino, and A. I. Caplan, 1996. Regulated expression of chondroitin sulfates at sites of epithelialmesenchymal interaction: spatio-temporal patterning identified with anti-chondroitin sulfate monoclonal antibodies. Int. J. Dev. Neurosci. 14:233-248.
52. Sorrell, J. M., F. Mahmoodian, I. A. Schafer, B. Davis, and B. Caterson, 1990. Identification of monoclonal antibodies that recognize novel epitopes in native chondroitin/ dermatan sulfate glycosaminoglycan chains: their use in mapping functionally distinct domains of human skin. J. Histochem. Cytochem. 38:393-402.
53. Stockdale, F. E., and H. Holtzer, 1961. DNA synthesis and myogenesis. Exp. Cell Res. 24:508-520.
54. Tucker, R. P., and C. A. Erickson, 1984. Morphology and behavior of quail neural crest cells in artificial three-dimensional extracellular matrices. Dev. Biol. 104:390-405.
55. Wasserman, L., A. Ber, and D. Allalouf, 1977. Use of thin-layer chromatography in the separation of disaccharides resulting from digestion of chondroitin sulfates with chondroitinases. J. Chromatogr. 136:342-347.
56. Wight, T. N., D. K. Heinegård, and V. C. Hascall, 1991. Proteoglycans: structure and function. Pages 45-78 in: Cell Biology of Extracellular Matrix. 2nd ed. E. D. Hay, ed. Plenum Press, New York, NY.
57. Wight, T. N., M. G. Kinsella, and E. E. Qwarnström, 1992. The role of proteoglycans in cell adhesion, migration and proliferation. Curr. Opin. Cell Biol. 4:793-801.
58. Yamagata, M., and K. Kimata, 1994. Repression of a malignant cell-substratum adhesion phenotype by inhibiting the production of the anti-adhesive proteoglycan, PG-M/ versican. J. Cell Sci. 107:2581-2590.
59. Yamagata, M., S. Saga, M. Kato, M. Bernfield, and K. Kimata 1993. Selective distributions of proteoglycans and their ligands in pericellular matrix of cultured fibroblasts: implications for their roles in cell-substratum adhesion. J. Cell Sci. 106:55-65.
60. Yamagata, M., S. Suzuki, S. K. Akiyama, K. M. Yamada, and K. Kimata, 1989. Regulation of cell-substrate adhesion by proteoglycans immobilized on extracellular substrates. J. Biol. Chem. 264:8012-8018.
61. Yanagishita, M., and V. C. Hascall, 1984. Proteoglycans synthesized by rat ovarian granulosa cells in culture: isolation, fractionation, and characterization of proteoglycans associated with the cell layer. J. Biol. Chem. 259: 10260-10269.
62. Yayon, A., M. Klagsburn, J. D. Esko, P. Leder, and D. M. Ornitz, 1991. Cell surface heparin-like molecules are required for binding of bFGF to its high affinity receptor. Cell 64:841-848.
63. Young, H. E., D. A. Carrino, and A. I. Caplan, 1990. Change in synthesis of sulfated glycoconjugates during muscle development, maturation and aging in embryonic to senescent CBF-1 mouse. Mech. Ageing Dev. 53:179-193.
64. Young, H. E., D. A. Carrino, and A. I. Caplan, 1989. Histochemical analysis of newly synthesized and accumulated sulfated glycosaminoglycans during musculogenesis in the embryonic chick leg. J. Morphol. 201:85-103.
65. Zimmermann, D. R., and E. Ruoslahti, 1989. Multiple domains of the large fibroblast proteoglycan, versican. EMBO J. 8: 2975-2981.