The influence of extracellular matrix derived from skeletal muscle tissue on the proliferation and differentiation of myogenic progenitor cells ex vivo

Biomaterials

Volumn 30, Issue 12, 2009, Pages 2393-2399

  Stern, Matthew M ^a   Myers, Regina L ^a   Hammam, Nevin ^a   Stern, Kathryn A ^a   Eberli, Daniel ^a   Kritchevsky, Stephen B ^a   Soker, Shay ^a   Van Dyke, Mark ^a  

^a WAKE FOREST SCHOOL OF MEDICINE   (United States)

Author keywords

Cell culture; Cell proliferation; Extracellular matrix; Muscle; Progenitor cell

Indexed keywords

CELL POPULATIONS; EX-VIVO; EXTRACELLULAR MATRIX; GROWTH SURFACES; MICROENVIRONMENT; MODEL SYSTEMS; MUSCLE FIBERS; MUSCLE PROGENITOR CELLS; MUSCLE REGENERATIONS; MYOBLASTS; MYOGENIC CELLS; PROGENITOR CELL; SKELETAL MUSCLES; STEM CELLS; SURFACE COATINGS;

BIOLOGICAL MATERIALS; CELL CULTURE; CELL PROLIFERATION; ELECTRIC DISCHARGE MACHINING; ENZYME ACTIVITY;

MUSCLE;

BIOMATERIAL;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL DIFFERENTIATION; CELL POPULATION; CELL PROLIFERATION; CONTROLLED STUDY; EX VIVO STUDY; EXTRACELLULAR MATRIX; HAMSTRING; MUSCLE CELL; MUSCLE MASS; MUSCLE REGENERATION; MUSCLE TISSUE; NONHUMAN; PRIORITY JOURNAL; QUADRICEPS FEMORIS MUSCLE; RAT; SKELETAL MUSCLE; STEM CELL;

ANIMALS; CELL DIFFERENTIATION; CELL PROLIFERATION; CELLS, CULTURED; EXTRACELLULAR MATRIX; MICE; MITOGEN-ACTIVATED PROTEIN KINASE 1; MITOGEN-ACTIVATED PROTEIN KINASE 3; MUSCLE CELLS; MUSCLE, SKELETAL; PHOSPHORYLATION; RATS; STEM CELLS;

RATTUS;

EID: 60549087344     PISSN: 01429612     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2008.12.069     Document Type: Article

References (50)

1. Mayer U. Integrins: redundant or important players in skeletal muscle?. J Biol Chem 278 17 (2003) 14587-14590
2. Baeg G.H., and Perrimon N. Functional binding of secreted molecules to heparan sulfate proteoglycans in Drosophila. Curr Opin Cell Biol 12 5 (2000) 575-580
3. Clark K.A., McElhinny A.S., Beckerle M.C., and Gregorio C.C. Striated muscle cytoarchitecture: an intricate web of form and function. Annu Rev Cell Dev Biol 18 (2002) 637-706
4. Sanes J.R. The basement membrane/basal lamina of skeletal muscle. J Biol Chem 278 15 (2003) 12601-12604
5. Cohn R.D., and Campbell K.P. Molecular basis of muscular dystrophies. Muscle Nerve 23 10 (2000) 1456-1471
6. Gamble H.J., Fenton J., and Allsopp G. Electron microscope observations on human fetal striated muscle. J Anat 126 Pt 3 (1978) 567-589
7. Mauro A. Satellite cell of skeletal muscle fibers. J Biophys Biochem Cytol 9 (1961) 493-495
8. Campion D.R. The muscle satellite cell: a review. Int Rev Cytol 87 (1984) 225-251
9. Grounds M.D., White J.D., Rosenthal N., and Bogoyevitch M.A. The role of stem cells in skeletal and cardiac muscle repair. J Histochem Cytochem 50 5 (2002) 589-610
10. Charge S.B., and Rudnicki M.A. Cellular and molecular regulation of muscle regeneration. Physiol Rev 84 1 (2004) 209-238
11. Blaschuk K.L., Guerin C., and Holland P.C. Myoblast alpha v beta3 integrin levels are controlled by transcriptional regulation of expression of the beta3 subunit and down-regulation of beta3 subunit expression is required for skeletal muscle cell differentiation. Dev Biol 184 2 (1997) 266-277
12. Boettiger D., Enomoto-Iwamoto M., Yoon H.Y., Hofer U., Menko A.S., and Chiquet-Ehrismann R. Regulation of integrin alpha 5 beta 1 affinity during myogenic differentiation. Dev Biol 169 1 (1995) 261-272
13. Buck C.A., and Horwitz A.F. Cell surface receptors for extracellular matrix molecules. Annu Rev Cell Biol 3 (1987) 179-205
14. Eklund L., Piuhola J., Komulainen J., Sormunen R., Ongvarrasopone C., Fassler R., et al. Lack of type XV collagen causes a skeletal myopathy and cardiovascular defects in mice. Proc Natl Acad Sci U S A 98 3 (2001) 1194-1199
15. Menko A.S., and Boettiger D. Occupation of the extracellular matrix receptor, integrin, is a control point for myogenic differentiation. Cell 51 1 (1987) 51-57
16. Nandan D., Clarke E.P., Ball E.H., and Sanwal B.D. Ethyl-3,4-dihydroxybenzoate inhibits myoblast differentiation: evidence for an essential role of collagen. J Cell Biol 110 5 (1990) 1673-1679
17. Osses N., and Brandan E. ECM is required for skeletal muscle differentiation independently of muscle regulatory factor expression. Am J Physiol Cell Physiol 282 2 (2002) C383-C394
18. Beach R.L., Burton W.V., Hendricks W.J., and Festoff B.W. Extracellular matrix synthesis by skeletal muscle in culture: proteins and effect of enzyme degradation. J Biol Chem 257 19 (1982) 11437-11442
19. Foster R.F., Thompson J.M., and Kaufman S.J. A laminin substrate promotes myogenesis in rat skeletal muscle cultures: analysis of replication and development using antidesmin and anti-BrdUrd monoclonal antibodies. Dev Biol 122 1 (1987) 11-20
20. Hauschka S.D., and Konigsberg I.R. The influence of collagen on the development of muscle clones. Proc Natl Acad Sci U S A 55 1 (1966) 119-126
21. Li A.A., MacDonald N.C., and Chang P.L. Effect of growth factors and extracellular matrix materials on the proliferation and differentiation of microencapsulated myoblasts. J Biomater Sci Polym Ed 14 6 (2003) 533-549
22. Lyles J.M., Amin W., and Weill C.L. Matrigel enhances myotube development in a serum-free defined medium. Int J Dev Neurosci 10 1 (1992) 59-73
23. Maley M.A., Davies M.J., and Grounds M.D. Extracellular matrix, growth factors, genetics: their influence on cell proliferation and myotube formation in primary cultures of adult mouse skeletal muscle. Exp Cell Res 219 1 (1995) 169-179
24. Bekoff A., and Betz W. Properties of isolated adult rat muscle fibres maintained in tissue culture. J Physiol 271 2 (1977) 537-547
25. Bischoff R. Proliferation of muscle satellite cells on intact myofibers in culture. Dev Biol 115 1 (1986) 129-139
26. Bischoff R. Analysis of muscle regeneration using single myofibers in culture. Med Sci Sports Exerc 21 5 Suppl. (1989) S164-S172
27. Yaffe D., and Saxel O. Serial passaging and differentiation of myogenic cells isolated from dystrophic mouse muscle. Nature 270 5639 (1977) 725-727
28. Robinson M.J., and Cobb M.H. Mitogen-activated protein kinase pathways. Curr Opin Cell Biol 9 2 (1997) 180-186
29. Campbell J.S., Wenderoth M.P., Hauschka S.D., and Krebs E.G. Differential activation of mitogen-activated protein kinase in response to basic fibroblast growth factor in skeletal muscle cells. Proc Natl Acad Sci U S A 92 3 (1995) 870-874
30. Gredinger E., Gerber A.N., Tamir Y., Tapscott S.J., and Bengal E. Mitogen-activated protein kinase pathway is involved in the differentiation of muscle cells. J Biol Chem 273 17 (1998) 10436-10444
31. 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 1 (2001) 104-115
32. Berkes C.A., and Tapscott S.J. MyoD and the transcriptional control of myogenesis. Semin Cell Dev Biol 16 4-5 (2005) 585-595
33. Fuchtbauer E.M., and Westphal H. MyoD and myogenin are coexpressed in regenerating skeletal muscle of the mouse. Dev Dyn 193 1 (1992) 34-39
34. Smith II C.K., Janney M.J., and Allen R.E. Temporal expression of myogenic regulatory genes during activation, proliferation, and differentiation of rat skeletal muscle satellite cells. J Cell Physiol 159 2 (1994) 379-385
35. Yablonka-Reuveni Z., and Rivera A.J. Temporal expression of regulatory and structural muscle proteins during myogenesis of satellite cells on isolated adult rat fibers. Dev Biol 164 2 (1994) 588-603
36. Conconi M.T., Bellini S., Teoli D., de Coppi P., Ribatti D., Nico B., et al. In vitro and in vivo evaluation of acellular diaphragmatic matrices seeded with muscle precursors cells and coated with VEGF silica gels to repair muscle defect of the diaphragm. J Biomed Mater Res A (2008)
37. De Coppi P., Bellini S., Conconi M.T., Sabatti M., Simonato E., Gamba P.G., et al. Myoblast-acellular skeletal muscle matrix constructs guarantee a long-term repair of experimental full-thickness abdominal wall defects. Tissue Eng 12 7 (2006) 1929-1936
38. Gamba P.G., Conconi M.T., Lo Piccolo R., Zara G., Spinazzi R., and Parnigotto P.P. Experimental abdominal wall defect repaired with acellular matrix. Pediatr Surg Int 18 5-6 (2002) 327-331
39. Fawcett J.W., and Keynes R.J. Muscle basal lamina: a new graft material for peripheral nerve repair. J Neurosurg 65 3 (1986) 354-363
40. Ide C. Nerve regeneration through the basal lamina scaffold of the skeletal muscle. Neurosci Res 1 (1984) 379-391
41. Fansa H., and Keilhoff G. Comparison of different biogenic matrices seeded with cultured Schwann cells for bridging peripheral nerve defects. Neurol Res 26 2 (2004) 167-173
42. Fansa H., Keilhoff G., Wolf G., Schneider W., and Gold B.G. Tissue engineering of peripheral nerves: a comparison of venous and acellular muscle grafts with cultured Schwann cells. Plast Reconstr Surg 107 2 (2001) 495-496
43. Feneley M.R., Fawcett J.W., and Keynes R.J. The role of Schwann cells in the regeneration of peripheral nerve axons through muscle basal lamina grafts. Exp Neurol 114 3 (1991) 275-285
44. Keilhoff G., Pratsch F., Wolf G., and Fansa H. Bridging extra large defects of peripheral nerves: possibilities and limitations of alternative biological grafts from acellular muscle and Schwann cells. Tissue Eng 11 7-8 (2005) 1004-1014
45. Mligiliche N., Kitada M., and Ide C. Grafting of detergent-denatured skeletal muscles provides effective conduits for extension of regenerating axons in the rat sciatic nerve. Arch Histol Cytol 64 1 (2001) 29-36
46. Mligiliche N., Tabata Y., Endoh K., and Ide C. Peripheral nerve regeneration through a long detergent-denatured muscle autografts in rabbits. Neuroreport 12 8 (2001) 1719-1722
47. Freytes D.O., Martin J., Velankar S.S., Lee A.S., and Badylak S.F. Preparation and rheological characterization of a gel form of the porcine urinary bladder matrix. Biomaterials 29 11 (2008) 1630-1637
48. Lan M.A., Gersbach C.A., Michael K.E., Keselowsky B.G., and Garcia A.J. Myoblast proliferation and differentiation on fibronectin-coated self assembled monolayers presenting different surface chemistries. Biomaterials 26 22 (2005) 4523-4531
49. Langen R.C., Schols A.M., Kelders M.C., Wouters E.F., and Janssen-Heininger Y.M. Enhanced myogenic differentiation by extracellular matrix is regulated at the early stages of myogenesis. In Vitro Cell Dev Biol Anim 39 3-4 (2003) 163-169
50. Cronin E.M., Thurmond F.A., Bassel-Duby R., Williams R.S., Wright W.E., Nelson K.D., et al. Protein-coated poly(l-lactic acid) fibers provide a substrate for differentiation of human skeletal muscle cells. J Biomed Mater Res A 69 3 (2004) 373-381