Decorin modulates collagen I-stimulated, but not fibronectin-stimulated, migration of C2C12 myoblasts

Matrix Biology

Volumn 30, Issue 2, 2011, Pages 109-117

  Goetsch, K P ^a   Kallmeyer, K ^a,b   Niesler, C U ^a  

^a UNIVERSITY OF KWAZULU NATAL   (South Africa)

^b UNIVERSITY OF PRETORIA   (South Africa)

Author keywords

Collagen I; Decorin; Fibronectin; Migration; Myoblast; ROCK

Indexed keywords

CELL PROTEIN; COLLAGEN TYPE 1; DECORIN; FIBRONECTIN; PROTEIN ROCK 2; UNCLASSIFIED DRUG;

ARTICLE; CELL ADHESION; CELL MIGRATION; CONTROLLED STUDY; MYOBLAST; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; WOUND CLOSURE;

ANIMALS; CATTLE; CELL LINE; CELL MOVEMENT; COLLAGEN TYPE I; DECORIN; DOSE-RESPONSE RELATIONSHIP, DRUG; FIBRONECTINS; FOCAL ADHESIONS; MICE; MYOBLASTS, SKELETAL; RHO-ASSOCIATED KINASES; WOUND HEALING;

EID: 79952100305     PISSN: 0945053X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.matbio.2010.10.009     Document Type: Article

References (46)

1. Bonnemann C.G., Laing N.G. Myopathies resulting from mutations in sarcomeric proteins. Curr. Opin. Neurol. 2004, 17:529-537.
2. Brandan E., Cabello-Verrugio C., Vial C. Novel regulatory mechanisms for the proteoglycans decorin and biglycan during muscle formation and muscular dystrophy. Matrix Biol. 2008, 27:700-708.
3. Bretscher M.S. Moving membrane up to the front of migrating cells. Cell 1996, 85:465-467.
4. Chrzanowska-Wodnicka M., Burridge K. Rho-stimulated contractility drives the formation of stress fibers and focal adhesions. J. Cell Biol. 1996, 133:1403-1415.
5. Droguett R., Cabello-Verrugio C., Riquelme C., Brandan E. Extracellular proteoglycans modify TGF-beta bio-availability attenuating its signaling during skeletal muscle differentiation. Matrix Biol. 2006, 25:332-341.
6. Ehrhardt J., Morgan J. Regenerative capacity of skeletal muscle. Curr. Opin. Neurol. 2005, 18:548-553.
7. Fiedler L.R., Schonherr E., Waddington R., Niland S., Seidler D.G., Aeschlimann D., Eble J.A. Decorin regulates endothelial cell motility on collagen I through activation of insulin-like growth factor I receptor and modulation of alpha2beta1 integrin activity. J. Biol. Chem. 2008, 283:17406-17415.
8. Fortier M., Comunale F., Kucharczak J., Blangy A., Charrasse S., Gauthier-Rouviere C. RhoE controls myoblast alignment prior fusion through RhoA and ROCK. Cell Death Differ. 2008, 15:1221-1231.
9. Friedl P., Brocker E.B. The biology of cell locomotion within three-dimensional extracellular matrix. Cell. Mol. Life Sci. 2000, 57:41-64.
10. Friedl P., Zanker K.S., Brocker E.B. Cell migration strategies in 3-D extracellular matrix: differences in morphology, cell matrix interactions, and integrin function. Microsc. Res. Tech. 1998, 43:369-378.
11. Fukushima K., Badlani N., Usas A., Riano F., Fu F., Huard J. The use of an antifibrosis agent to improve muscle recovery after laceration. Am. J. Sports Med. 2001, 29:394-402.
12. Fukushima H., Ohsawa M., Ikura Y., Naruko T., Sugama Y., Suekane T., Kitabayashi C., Inoue T., Hino M., Ueda M. Mast cells in diffuse large B-cell lymphoma; their role in fibrosis. Histopathology 2006, 49:498-505.
13. Gatchalian C.L., Schachner M., Sanes J.R. Fibroblasts that proliferate near denervated synaptic sites in skeletal muscle synthesize the adhesive molecules tenascin (J1), N-CAM, fibronectin, and a heparan sulfate proteoglycan. J. Cell Biol. 1989, 108:1873-1890.
14. Gelse K., Poschl E., Aigner T. Collagens - structure, function, and biosynthesis. Adv. Drug Deliv. Rev. 2003, 55:1531-1546.
15. Heino J. Biology of tumor cell invasion: interplay of cell adhesion and matrix degradation. Int. J. Cancer 1996, 65:717-722.
16. Hocking D.C., Titus P.A., Sumagin R., Sarelius I.H. Extracellular matrix fibronectin mechanically couples skeletal muscle contraction with local vasodilation. Circ. Res. 2008, 102:372-379.
17. Humphries J.D., Byron A., Humphries M.J. Integrin ligands at a glance. J. Cell Sci. 2006, 119:3901-3903.
18. Jarvinen T.A., Jarvinen T.L., Kaariainen M., Aarimaa V., Vaittinen S., Kalimo H., Jarvinen M. Muscle injuries: optimising recovery. Best Pract. Res. Clin. Rheumatol. 2007, 21:317-331.
19. Kalamajski S., Aspberg A., Oldberg A. The decorin sequence SYIRIADTNIT binds collagen type I. J. Biol. Chem. 2007, 282:16062-16067.
20. Kawano Y., Fukata Y., Oshiro N., Amano M., Nakamura T., Ito M., Matsumura F., Inagaki M., Kaibuchi K. Phosphorylation of myosin-binding subunit (MBS) of myosin phosphatase by Rho-kinase in vivo. J. Cell Biol. 1999, 147:1023-1038.
21. Keene D.R., San Antonio J.D., Mayne R., McQuillan D.J., Sarris G., Santoro S.A., Iozzo R.V. Decorin binds near the C terminus of type I collagen. J. Biol. Chem. 2000, 275:21801-21804.
22. Kishioka Y., Thomas M., Wakamatsu J., Hattori A., Sharma M., Kambadur R., Nishimura T. Decorin enhances the proliferation and differentiation of myogenic cells through suppressing myostatin activity. J. Cell. Physiol. 2008, 215:856-867.
23. Kjaer M. Role of extracellular matrix in adaptation of tendon and skeletal muscle to mechanical loading. Physiol. Rev. 2004, 84:649-698.
24. Kresse H., Liszio C., Schonherr E., Fisher L.W. Critical role of glutamate in a central leucine-rich repeat of decorin for interaction with type I collagen. J. Biol. Chem. 1997, 272:18404-18410.
25. Lehto M., Jarvinen M. Collagen and glycosaminoglycan synthesis of injured gastrocnemius muscle in rat. Eur. Surg. Res. 1985, 17:179-185.
26. Miura T., Kishioka Y., Wakamatsu J., Hattori A., Hennebry A., Berry C.J., Sharma M., Kambadur R., Nishimura T. Decorin binds myostatin and modulates its activity to muscle cells. Biochem. Biophys. Res. Commun. 2006, 340:675-680.
27. Nobes C.D., Hall A. Rho, rac, and cdc42 GTPases regulate the assembly of multimolecular focal complexes associated with actin stress fibers, lamellipodia, and filopodia. Cell 1995, 81:53-62.
28. Olguin H.C., Santander C., Brandan E. Inhibition of myoblast migration via decorin expression is critical for normal skeletal muscle differentiation. Dev. Biol. 2003, 259:209-224.
29. Papusheva E., Heisenberg C.P. Spatial organization of adhesion: force-dependent regulation and function in tissue morphogenesis. EMBO J. 2010, 29:2753-2768.
30. Quintero A.J., Wright V.J., Fu F.H., Huard J. Stem cells for the treatment of skeletal muscle injury. Clin. Sports Med. 2009, 28:1-11.
31. Ranzato E., Balbo V., Boccafoschi F., Mazzucco L., Burlando B. Scratch wound closure of C2C12 mouse myoblasts is enhanced by human platelet lysate. Cell Biol. Int. 2009, 33:911-917.
32. Ricard-Blum S., Ruggiero F. The collagen superfamily: from the extracellular matrix to the cell membrane. Pathol. Biol. (Paris) 2005, 53:430-442.
33. Ridley A.J., Hall A. Distinct patterns of actin organization regulated by the small GTP-binding proteins Rac and Rho. Cold Spring Harb. Symp. Quant. Biol. 1992, 57:661-671.
34. Ridley A.J., Hall A. The small GTP-binding protein rho regulates the assembly of focal adhesions and actin stress fibers in response to growth factors. Cell 1992, 70:389-399.
35. Ruhland C., Schonherr E., Robenek H., Hansen U., Iozzo R.V., Bruckner P., Seidler D.G. The glycosaminoglycan chain of decorin plays an important role in collagen fibril formation at the early stages of fibrillogenesis. FEBS J. 2007, 274:4246-4255.
36. Sato M., Markiewicz M., Yamanaka M., Bielawska A., Mao C., Obeid L.M., Hannun Y.A., Trojanowska M. Modulation of transforming growth factor-beta (TGF-beta) signaling by endogenous sphingolipid mediators. J. Biol. Chem. 2003, 278:9276-9282.
37. Schmidt G., Hausser H., Kresse H. Interaction of the small proteoglycan decorin with fibronectin. Involvement of the sequence NKISK of the core protein. Biochem. J. 1991, 280(Pt 2):411-414.
38. Schmitz A.A., Govek E.E., Bottner B., Van Aelst L. Rho GTPases: signaling, migration, and invasion. Exp. Cell Res. 2000, 261:1-12.
39. Sheffer Y., Leon O., Pinthus J.H., Nagler A., Mor Y., Genin O., Iluz M., Kawada N., Yoshizato K., Pines M. Inhibition of fibroblast to myofibroblast transition by halofuginone contributes to the chemotherapy-mediated antitumoral effect. Mol. Cancer Ther. 2007, 6:570-577.
40. Sulochana K.N., Fan H., Jois S., Subramanian V., Sun F., Kini R.M., Ge R. Peptides derived from human decorin leucine-rich repeat 5 inhibit angiogenesis. J. Biol. Chem. 2005, 280:27935-27948.
41. Svensson L., Heinegard D., Oldberg A. Decorin-binding sites for collagen type I are mainly located in leucine-rich repeats 4-5. J. Biol. Chem. 1995, 270:20712-20716.
42. Thorrez L., Shansky J., Wang L., Fast L., VandenDriessche T., Chuah M., Mooney D., Vandenburgh H. Growth, differentiation, transplantation and survival of human skeletal myofibers on biodegradable scaffolds. Biomaterials 2008, 29:75-84.
43. Watanabe N., Kato T., Fujita A., Ishizaki T., Narumiya S. Cooperation between mDia1 and ROCK in Rho-induced actin reorganization. Nat. Cell Biol. 1999, 1:136-143.
44. Weber I.T., Harrison R.W., Iozzo R.V. Model structure of decorin and implications for collagen fibrillogenesis. J. Biol. Chem. 1996, 271:31767-31770.
45. Yaffe D., Saxel O. A myogenic cell line with altered serum requirements for differentiation. Differentiation 1977, 7:159-166.
46. Zhu J., Li Y., Shen W., Qiao C., Ambrosio F., Lavasani M., Nozaki M., Branca M.F., Huard J. Relationships between transforming growth factor-beta1, myostatin, and decorin: implications for skeletal muscle fibrosis. J. Biol. Chem. 2007, 282:25852-25863.