Laminin chains in developing and adult human myotendinous junctions

Journal of Histochemistry and Cytochemistry

Volumn 48, Issue 2, 2000, Pages 201-209

  Pedrosa Domellöf, Fatima ^a,b   Tiger, Carl Fredrik ^d   Virtanen, Ismo ^c   Thornell, Lars Eric ^a,b   Gullberg, Donald ^d  

^a UMEÅ UNIVERSITY   (Sweden)

^b NATIONAL INSTITUTE FOR WORKING LIFE   (Sweden)

^c UNIVERSITY OF HELSINKI   (Finland)

^d UPPSALA UNIVERSITY   (Sweden)

Author keywords

Development; Human; Laminin 1 chain; Muscle; Myotendinous junction

Indexed keywords

LAMININ; MONOCLONAL ANTIBODY; POLYCLONAL ANTIBODY; TENASCIN;

ARTICLE; BASEMENT MEMBRANE; CONTROLLED STUDY; FETUS; HUMAN; HUMAN TISSUE; IMMUNOBLOTTING; IMMUNOCYTOCHEMISTRY; LEG MUSCLE; MUSCLE BIOPSY; MUSCLE DEVELOPMENT; PRIORITY JOURNAL; PROTEIN LOCALIZATION; SKELETAL MUSCLE;

EID: 0034000155     PISSN: 00221554     EISSN: None     Source Type: Journal    
DOI: 10.1177/002215540004800205     Document Type: Article

References (39)

1. Aumailley M, Smyth N (1998) The role of laminins in basement membrane function. J Anat 193:1-21
2. Baumeister A, Arber S, Caroni P (1997) Accumulation of muscle ankyrin repeat protein transcript reveals local activation of primary myotube endcompartments during muscle morphogenesis. J Cell Biol 139:1231-1242
3. Becker S, Pasca G, Strumpf D, Min L, Volk T (1997) Reciprocal signaling between Drosophila epidermal muscle attachment cells and their corresponding muscles. Development 124:2615-2622
4. Benjamin M, Ralphs JR (1997) Tendon and ligaments - an overview. Histol Histopathol 12:1135-1144
5. Campbell KP (1995) Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage. Cell 80:675-679
6. Chiquet M, Fambrough DM (1984) Chick myotendinous antigen. I. A monoclonal antibody as a marker for tendon and muscle morphogenesis. J Cell Biol 98:1926-1936
7. Durbeej M, Henry MD, Campbell KP (1998) Dystroglycan in development and disease. Curr Opin Cell Biol 10:594-601
8. Duxon MJ, Usson Y (1989) Cellular insertion of primary and secondary myotubes in embryonic rat muscles. Development 107: 243-251
9. Ekblom M, Klein G, Mugrauer G, Fecker L, Deutzmann R, Timpl R, Ekblom P (1990) Transiently and locally restricted expression of laminin A chain mRNA by developing epithelial cells during kidney organogenesis. Cell 60:337-346
10. Engvall E, Earwicker D, Haaparanta T, Ruoslahti E, Sanes JR (1990) Distribution and isolation of four laminin variants: tissue restricted distribution of heterotrimers assembled from five different subunits. Cell Regul 1:731-740
11. Gullberg D, Tiger CF, Velling T (1999) Laminins during muscle development and in muscular dystrophies. Cell Mol Life Sci 56:442-460
12. Gullberg D, Veiling T, Lohikangas L, Tiger CF (1998) Integrins during muscle development and in muscular dystrophies. Front Biosci 9:1028-1039
13. Gullberg D, Veiling T, Sjöberg G, Salmivirta K, Gaggero B, Edström L, Sejersen T (1997) Tenascin-C expression correlates to macrophage invasion in Duchenne muscular dystrophy and in myositis. Neuromusc Disord 7:39-54
14. Hauschka SD (1994) The embryonic origin of muscle. In Engel AG, Franzini-Armstrong C, eds. Myology. 2nd ed. New York, McGraw Hill, 3-73
15. Hayashi YK, Chou F-L, Engvall E, Ogawa M, Matsuda C, Hirabayashi S, Yokochi K, Ziober BL, Kramer RH, Kaufman SJ, Ozawa E, Goto Y, Nonaka I, Tsukahara T, Wang J-Z, Hoffman EP, Arahata K (1998) Mutations in the integrin α7 gene cause congenital myopathy. Nature Genet 19:94-97
16. Helbling-Leclerc A, Zhang X, Topaloglu H, Cruaud C, Tesson F, Weissenbach J, Tome FM, Schwartz K, Fardeau M, Tryggvason K, Guicheny P (1995) Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy. Nature Genet 11:216-218
17. Hillaire D, Leclerc A, Faure S, Topaloglu H, Chiannilkulchai N, Guicheney P, Grinas L, Legos P, Philpot J, Evangelista T, Routon MC, Mayer M, Pellissier JF, Estournet B, Barois A, Hentati F, Feingold N, Beckmann JS, Dubowitz V, Tome FMS, Fardeau M (1994) Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping. Hum Mol Genet 3:1657-1661
18. Hughes S, Cho M, Karsch-Mizrachi I, Travis M, Silberstein L, Leinwand LA, Blau HM (1993) Three slow myosin heavy chains sequentially expressed in developing mammalian skeletal muscle. Dev Biol 158:183-199
19. Hunter DD, Shah V, Merlie JP, Sanes JR (1989) A laminin-like adhesive protein concentrated in the synaptic cleft of the neuromuscular junction. Nature 338:229-234
20. Iivanainen A, Kortesmaa J, Sahlberg C, Morita T, Bergmann U, Thesleff I, Tryggvason K (1997) Primary structure, developmental expression, and immunolocalization of the murine laminin 4 chain. J Biol Chem 272:27862-27868
21. Jobsis GJ, Keizers H, Vreijling JP, de Visser M, Speer MC, Wolterman RA, Baas F, Bolhuis PA (1996) Type VI collagen mutations in Bethlehem myopathy, an autosomal dominant myopathy with contractures. Nature Genet 14:113-115
22. Koch M, Olson PF, Albus A, Jin W, Hunter DD, Brunken WJ, Burgeson RE, Champliaud MF (1999) Characterization and expression of the laminin γ3 chain: a novel, non-basement membrane-associated, laminin chain. J Cell Biol 145:605-618
23. Kühl U, Öcalan M, Timpl R, Mayne R, Hay E, von der Mark K (1984) Role of muscle fibroblasts in the deposition of type IV collagen in the basal lamina of myotubes. Differentiation 28: 164-172
24. Mayer U, Saher G, Fassler R, Bornemann A, Echtermeyer F, von der Mark H, Miosge N, Poschl E, von der Mark K (1997) Absence of integrin alpha 7 causes a novel form of muscular dystrophy. Nature Genet 17:318-323
25. Monical PL, Kefalides NA (1994) Coculture modulate laminin synthesis and mRNA levels in epidermal keratinocytes and dermal fibroblasts. Exp Cell Res 210:154-159
26. Patton BL, Miner JH, Chiu AY, Sanes JR (1997) Distribution and function of laminins in the neuromuscular system of developing, adult, and mutant mice. J Cell Biol 139:1507-1521
27. Richards A, Al-Imara L, Pope FM (1996) The complete cDNA sequence of laminin α4 and its relationship to the other human laminin α chains. Eur J Biochem 238:813-821
28. Rousselle P, Lunstrum GP, Keene DR, Burgeson RE (1991) Kalinin: an epithelium-specific basement membrane adhesion molecule that is a component of anchoring filaments. J Cell Biol 114:567-576
29. Sanderson RD, Fitch JM, Linsenmayer TR, Mayne R (1986) Fibroblasts promote the formation of a continous basal lamina during myogenesis in vitro. J Cell Biol 102:740-747
30. Schuler F, Sorokin L (1995) Expression of laminin isoforms in mouse myogenic cells in vitro and in vivo. J Cell Sci 108:3795-3805
31. Senga K, Kobayashi M, Hattori H, Yasue K, Mizutani H, Ueda M, Hoshino T (1995) Type VI collagen in mouse masseter tendon, from osseous attachment to myotendinous junction. Anat Rec 243:294-302
32. Song WK, Wang W, Foster RF, Bielser DA, Kaufman SJ (1992) H36-α7 is a novel integrin alpha chain that is developmentally regulated during skeletal myogenesis. J Cell Biol 117:643-657
33. Tidball JG, Lin C (1989) Structural changes at the myogenic cell surface during the formation of the myotendinous junction. Cell Tissue Res 257:77-84
34. Tiger CF, Champliaud MF, Pedrosa-Domellöf F, Thornell LE, Gullberg D (1997) Presence of laminin alpha5 chain and lack of laminin alpha1 chain during human muscle development and in muscular dystrophies. J Biol Chem 272:28590-28595
35. Tiitta O, Wahlström T, Paavonen J, Linnala A, Sharma S, Gould VE, Virtanen I (1992) Enhanced tenascin expression in cervical and vulvar koilocytic lesions. Am J Pathol 141:907-913
36. Timpl R (1996) Macromolecular organization of basement membranes. Curr Opin Cell Biol 8:618-624
37. Wewer UM, Thornell LE, Loechel F, Zhang X, Durkin ME, Amano S, Burgeson RE, Engvall E, Albrechtsen R, Virtanen I (1997) Extrasynaptic location of laminin beta 2 chain in developing and adult human skeletal muscle. Am J Pathol 151:621-631
38. Xu H, Christmas P, Wu XR, Wewer UM, Engvall E (1994a) Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse. Proc Natl Acad Sci USA 91:5572-5576
39. Xu H, Wu XR, Wewer UM, Engvall E (1994b) Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene. Nature Genet 8:297-302