Laminin α4 and integrin α6 are upregulated in regenerating dy/dy skeletal muscle: Comparative expression of laminin and integrin isoforms in muscles regenerating after crush injury

Experimental Cell Research

Volumn 256, Issue 2, 2000, Pages 500-514

  Sorokin, Lydia M ^a   Maley, Moira A L ^b   Moch, Helga ^c   Von Der Mark, Helga ^c   Von Der Mark, Klaus ^c   Cadalbert, Laurence ^a   Karosi, Stefanie ^a   Davies, Marilyn J ^a   McGeachie, John K ^a   Grounds, Miranda D ^a  

^a Interdisciplinary Center for Clinical Research   (Germany)

^b UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^c UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA6 INTEGRIN; INTEGRIN; INTEGRIN ALPHA7BETA1; ISOPROTEIN; LAMA4 PROTEIN, MOUSE; LAMININ; LAMININ A; LAMININ ALPHA2; LAMININ ALPHA5; LEUKOCYTE ANTIGEN; VERY LATE ACTIVATION ANTIGEN 3; VERY LATE ACTIVATION ANTIGEN 6; MEMBRANE PROTEIN;

ANIMAL; ARTICLE; ENZYME IMMUNOASSAY; FLUORESCENT ANTIBODY TECHNIQUE; INJURY; METABOLISM; MOUSE; PHYSIOLOGY; REGENERATION; SKELETAL MUSCLE; UPREGULATION; ANIMAL EXPERIMENT; ANIMAL MODEL; BASEMENT MEMBRANE; CELL DIFFERENTIATION; CONTROLLED STUDY; CRUSH TRAUMA; ENDOTHELIUM CELL; FIBROBLAST; INFLAMMATORY CELL; MONONUCLEAR CELL; MUSCLE REGENERATION; MYOTUBE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; RECEPTOR UPREGULATION; SATELLITE CELL;

ANIMALS; ANTIGENS, CD; FLUORESCENT ANTIBODY TECHNIQUE; IMMUNOENZYME TECHNIQUES; INTEGRIN ALPHA3BETA1; INTEGRIN ALPHA6; INTEGRIN ALPHA6BETA1; INTEGRINS; LAMININ; MICE; MUSCLE, SKELETAL; PROTEIN ISOFORMS; REGENERATION; UP-REGULATION;

EID: 0034178263     PISSN: 00144827     EISSN: None     Source Type: Journal    
DOI: 10.1006/excr.2000.4842     Document Type: Article

References (58)

1. Grounds M. D. Towards understanding skeletal muscle regeneration. Pathol. Res. Pract. 187:1991;1-22.
2. Grounds M. D., McGeachie J. K., Davies M. J., Sorokin L. M., Maley M. A. L. The expression of extracellular matrix during adult skeletal muscle regeneration: How the basement membrane, interstitium and myogenic cells collaborate. Basic Appl. Myol. 8:1998;129-142.
3. Grounds M. Muscle regeneration: Molecular aspects and therapeutic implications. Curr. Opin. Neurol. 12:1999;535-543.
4. Kühl U., Ocalan M., Timpl R., von der Mark K. Role of laminin and fibronectin in selecting myogenic versusfibrogenic cells from skeletal muscle cells in vitro. Dev. Biol. 117:1986;628-635.
5. Schuler F., Sorokin L. M. Expression of laminin isoforms in mouse myogenic cells in vitro and in vivo. J. Cell Sci. 108:1995;3795-3805.
6. von der Mark K., Öcalan M. Antagonistic effects of laminin and fibronectin on the expression of the myogenic phenotype. Differentiation. 40:1989;150-157.
7. von der Mark H., Durr J., Sonneberg A., von der Mark K., Deutzmann R., Goodman S. L. Skeletal myoblasts utilize a novel β1-series integrin for binding to the E8 and T8 fragments of laminin. J. Biol. Chem. 266:1991;23593-23601.
8. Kramer R. H., Vu M. P., Cheng Y.-F., Ramos D. M., Timpl R., Waleh N. Laminin-binding integrin α7β1: Functional characterization and expression in normal and malignant melanocytes. Cell Regul. 2:1991;805-817.
9. Durbeej M., Henry M., Campbell K. P. Dystroglycan in development and disease. Curr. Opin. Cell Biol. 10:1998;594-601.
10. Straub V., Campbell K. P. Muscular dystrophies and the dystrophin-glycoprotein complex. Curr. Opin. Neurol. 10:1997;168-175.
11. Gee S. H., Blacher R. W., Douville P. J., Provost P. R., Yurchenco P. D., Carbonetto S. Laminin-binding protein 120 from brain is closely related to the dystrophin-associated glycoprotein, dystroglycan, and binds with high affinity to the major heparin binding domain of laminin. J. Biol. Chem. 268:1993;14972-14980.
12. Talts J. F., Andac Z., Göhring W., Brancaccio A., Timpl R. Binding of G domains of laminin alpha 1 and alpha 2 chains and perlecan to heparin, sulfatides, alpha-dystroglycan and several extracellular matrix proteins. EMBO J. 18:1999;863-870.
13. Grady R. M., Granger R. W., Lau K. S., Maimone M. M., Nichol M. C., Stull J. T., Sanes J. R. Role for α-dystrobrevin in the pathogenesis of dystrophin-dependent muscular dystrophies. Nature Cell Biol. 1:1999;215-220.
14. Lim L. E., Campbell K. P. The sarcoglycan complex in limb-girdle muscular dystrophy. Curr. Opin. Neurol. 11:1998;443-452.
15. Xu H., Wu X. R., Wewer U. M., Engvall E. Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene. Nature Genet. 8:1994;297-302.
16. Miyagoe Y., Hanaoka K., Nonaka I., Hayasaka M., Nabeshima Y., Arahata K., Nabeshima Y., Takeda S. Laminin alpha 2 chain-null mutant mice by targeted disruption of the LamA2 gene: A new model of merosin (laminin-2)-deficient congenital muscular dystrophy. FEBS Lett. 415:1997;33-39.
17. Arahata K., Ishii H., Hayashi Y. K. Congenital muscular dystrophies. Curr. Opin. Neurol. 8:1995;385-390.
18. Mayer U., Saher G., Fässler R., Bornemann A., Echtermeyer F., von der Mark H., Miosge N., Pöschl E., von der Mark K. Absence of integin alpha 7 causes a novel form of muscular dystrophy. Nature Genet. 17:1997;318-323.
19. Hayashi Y. K., Chou F.-L., Engvall E., Ogawa M., Matsuda C., Hirabayashi S., Yokochi K., Ziober B. L., Kramer R. H., Kaufman S. Mutations in the integrin α7 gene cause congenital myopathy. Nature Genet. 19:1998;94-97.
20. Frieser M., Nöckel H., Pausch F., Röder C., Hahn A., Deutzmann R., Sorokin L. M. Cloning of the mouse laminin alpha 4 gene: Expression in a subset of endothelium. Eur. J. Biochem. 246:1997;727-735.
21. Sorokin L. M., Frieser M., Pausch F., Kröger S., Ohage E., Deutzmann R. Developmental regulation of laminin alpha 5 implicates a role in epithelial and endothelial cell maturation. Dev. Biol. 189:1997;285-300.
22. Ringelmann B., Röder C., Hallmann R., Maley M., Davies M., Grounds M., Sorokin L. M. Expression of laminin α1, α2, α4 and α5 chains, fibronectin and tenascin-C in skeletal muscle of dystrophic 129ReJ dy/dy mice. Exp. Cell Res. 246:1999;165-182.
23. Patton B. L., Miner J. H., Chiu A. Y., Sanes J. R. Distribution and function of laminin in the neuromuscular system of the developing adult and mutant mice. J. Cell Biol. 139:1997;1507-1523.
24. Sewry C. A., Philpot J., Mahony D., Wilson L. A., Muntoni F., Dubowitz V. Expression of laminin subunits in congenital muscular dystrophy. Neuromusc. Disord. 5:1995;307-316.
25. Mitchell C. A., McGeachie J. K., Grounds M. D. Cellular differences in the regeneration of murine skeletal muscle-aquantitative histological study in SJL/J and BALB/c mice. Cell Tissue Res. 269:1992;159-166.
26. Lazarides E., Granger B. L. Fluorescent localization of membrane sites in glycerinated chicken skeletal muscle fibers and the relationship of these sites to the protein composition of the Z disc. Proc. Natl. Acad. Sci. USA. 75:1978;3683-3687.
27. Kaufman S. J., Foster R. F. Replicating myoblasts express a muscle-specific phenotype. Proc. Natl. Acad. Sci. USA. 85:1988;9606-9610.
28. Lawson M. J., McGeachie J. The identification of myogenic cells in skeletal muscle, with emphasis on the use of tritiated thymidine autoradiography and desmin antibodies. J. Anat. 192:1998;161-171.
29. Echtermeyer F., Schöber S., Pöschl E., von der Mark H., von der Mark K. Specific induction of cell motility on laminin by α7 integrin. J. Biol. Chem. 271:1996;2071-2075.
30. Cohn R. D., Mayer U., Saher G., Herrmann R., van der Flier A., Sonnenberg A., Sorokin L., Voit T. Secondary reduction of α7B integrin in laminin α2 deficient congenital muscular dystrophy supports an additional transmembrane link in skeletal muscle. J. Neurol. Sci. 163:1999;140-152.
31. Vecchi A., Garlanda C., Lampugnani M. G., Resnati M., Matteucci C., Stoppacciaro A., Schnürch H., Risau W., Ruco L., Mantovani A. Monoclonal antibodies specific for endothelial cells of mouse blood vessels. Their application in the identification of adult and embryonic endothelium. Eur. J. Cell Biol. 63:1994;247-254.
32. Maley M. A., Fan Y., Beilharz M. W., Grounds M. D. Intrinsic differences in MyoD and myogenin expression between primary cultures of SJL/J and BALB/C skeletal muscle. Exp. Cell Res. 211:1994;99-107.
33. Frieser M., Hallmann R., Johansson S., Vestweber D., Goodman S. L., Sorokin L. Mouse polymorphonuclear granulocyte binding to extracellular matrix molecules involves beta 1 integrins. Eur. J. Immunol. 26:1996;3127-3136.
34. Bornemann A., Schmalbruch H. Desmin and vimentin in regenerating muscles. Muscle Nerve. 15:1992;14-20.
35. Galliano M.-F., Aberdam D., Aguzzi A., Ortonne J.-P., Meneguzzi G. Cloning and complete primary structure of the mouse laminin α3 chain. J. Biol. Chem. 270:1995;21820-21826.
36. Song W. K., Wang W., Sato H., Bielser D. A., Kaufman S. J. Expression of α7 integrin cytoplasmic domains during skeletal muscle development: Alternative forms, confromational change and homologies with serine/threonine kinases and tyrosine phosphatases. J. Cell Sci. 106:1993;1139-1152.
37. Vachon P. H., Xu H., Loechel F., Hayashi Y., Arachata K., Reed J. C., Wewer U. M., Engvall E. Integrins (α7β1) in muscle function and survival. Disrupted expression in merosin-deficient congenital muscular dystrophy. J. Clin. Invest. 100:1997;1870-1881.
38. Bourke D. B., Ontell M. Modification of the phenotypic expression of murine dystrophy: A morphological study. Anat. Rec. 214:1986;17-24.
39. Bourke D. L., Ontell M., Taylor F. Spontaneous regeneration of older dystrophic muscle does not reflect its regenerative capacity. Am. J. Anat. 181:1988;1-11.
40. Martin H., Ontell M. Regeneration of dystrophic muscle following multiple injections of Bupivacaine. Muscle Nerve. 11:1988;588-596.
41. Grounds M. D., Davies M. J. Chemotaxis in myogenesis. Basic Appl. Myol. 6:1996;469-483.
42. Witkowski J. A. Tissue culture studies of muscle disorders. Part 2. Biochemical studies, nerve-muscle culture, metabolic myopathies, and animal models. Muscle Nerve. 9:1986;283-298.
43. Kuang W., Xu H., Vachon P. H., Engvall E. Disruption of the lama2 gene in embryonic stem cells: Laminin α2 is necessary for sustenance of mature muscle cells. Exp. Cell Res. 241:1998;117-125.
44. Ocalan M., Goodman S. L., Kuhl U., Hauschka S. D., von der Mark K. Laminin alters cell shape and stimulates motility and proliferation of murine skeletal myoblasts. Dev. Biol. 125:1988;158-167.
45. Goodman S. L., Risse G., von der Mark K. The E8 fragment of laminin promotes the locomotion of myoblasts over extracellular matrix. J. Cell Biol. 109:1989;799-809.
46. Delwel G. O., Sonnenberg A. Laminin isoforms and their integrin receptors. Horton M. A. Adhesion Receptors as Therapeutic Targets. 1996;CRC Press, London.
47. Yao C. C., Ziober B. L., Sutherland A. E., Mendrick D. L., Kramer R. H. Laminins promote the locomotion of skeletal myoblasts via the α7 integrin receptor. J. Cell Sci. 109:1996;3139-3150.
48. George-Weinstein M., Foster R. F., Gerhart J. V., Kaufman S. J. In vitro and in vivo expression of α7 integrin and desmin define the primary and secondary myogenic lineages. Dev. Biol. 156:1993;209-229.
49. Georges-Labouesse E., Messadeq N., Yehia G., Cadalbert L., Dierich A., Le Meur M. Absence of integrin α6 leads to epidermolysis bullosa and neonatal death in mice. Nature Genet. 13:1996;370-373.
50. Taverna D., Disatnik M. H., Rayburn H., Bronson R. T., Yang J., Rando T. A., Hynes R. O. Dystrophic muscle in mice chimeric for expression of alpha 5 integrin. J. Cell Biol. 143:1998;849-859.
51. Rosen G. D., Sanes J. R., LaChance R., Cunningham J. M., Roman J., Dean D. C. Roles for the integrin VLA-4 and its counter receptor VCAM-1 in myogenesis. Cell. 69:1992;1107-1119.
52. Palmer E. L., Rüegg C., Ferrando R., Pytela R., Sheppard D. Sequence and tissue distribution of the integrin α9 subunit, a novel partner of β1 that is widely distributed in epithelia and muscle. J. Cell Biol. 123:1993;1289-1297.
53. Gullberg D., Sjöberg G., Velling T., Sejersen T. Analysis of fibronectin and vitronectin receptors on human fetal skeletal muscle cells upon differentiation. Exp. Cell Res. 220:1995;112-123.
54. Velling T., Kusche-Gullberg M., Sejersen T., Gullberg D. cDNA cloning and chromosomal localization of human α11 integrin. J. Biol. Chem. 274:1999;25735-25742.
55. Sorokin L. M., Conzelmann S., Ekblom P., Aumailley M., Battaglia C., Timpl R. Monoclonal antibodies against laminin A chain fragment E3 and their effects on cell- and heparin-binding, and on kidney development. Exp. Cell Res. 201:1992;137-144.
56. Valles A. M., Boyer B., Tarone G., Thiery J.-P. Alpha 2 beta 1 integrin is required for the collagen and FGF-1 induced cell dispersion in a rat bladder carcinoma cell line. Cell Adhesion Commun. 4:1996;187-199.
57. Sonnenberg A., Modderman P. W., Hogervorst F. Laminin receptor on platelets is the integrin VLA-6. Nature. 336:1988;487-489.
58. Lenter M., Vestweber D. The integrin chain beta 1 and alpha 6 associate with the chaperone calnexin prior to integrin assembly. J. Biol. Chem. 269:1994;122263-122268.