Formation of triads without the dihydropyridine receptor subunits in cell lines from dysgenic skeletal muscle

Journal of Cell Biology

Volumn 134, Issue 2, 1996, Pages 375-387

  Powell, Jeanne A ^a   Petherbridge, Lee ^b   Flucher, Bernhard E ^c  

^a SMITH COLLEGE   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c UNIVERSITY OF INNSBRUCK   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM ION; DIHYDROPYRIDINE; RECEPTOR SUBUNIT; RYANODINE RECEPTOR; VIRUS LARGE T ANTIGEN;

ANIMAL CELL; ARTICLE; CALCIUM TRANSPORT; CELL FUSION; CELL MUTANT; CONTROLLED STUDY; DEPOLARIZATION; EXCITATION CONTRACTION COUPLING; GENETIC TRANSFECTION; MYOBLAST; MYOTUBE; NONHUMAN; PRIORITY JOURNAL; RAT; SARCOPLASMIC RETICULUM; SKELETAL MUSCLE; TRANSVERSE TUBULAR SYSTEM;

ANIMALS; CALCIUM CHANNELS; CALCIUM CHANNELS, L-TYPE; CELL LINE; MEMBRANE FUSION; MUSCLE PROTEINS; MUSCLE, SKELETAL; RATS; RYANODINE RECEPTOR CALCIUM RELEASE CHANNEL;

EID: 0029998336     PISSN: 00219525     EISSN: None     Source Type: Journal    
DOI: 10.1083/jcb.134.2.375     Document Type: Article

References (53)

1. Adams, B.A., and K.G. Beam. 1989. A novel calcium current in dysgenic skeletal muscle. J. Gen. Physiol. 94:429-444.
2. Adams, B.A., T. Tanabe, A. Mikami, S. Numa, and K.G. Beam. 1990. Intramembrane charge movement restored in dysgenic skeletal muscle by injection of dihydropyridine receptor cDNAs. Nature (Lond.). 346:569-572.
3. Banker, B.Q. 1977. Muscular dysgenesis in the mouse (mdg/mdg). I. Ultrastructural study of skeletal and cardiac muscle. J. Neuropathol. Exp. Neurol. 36: 100-127.
4. Beam, K.G., C.M. Knudson, and J.A. Powell. 1986. A lethal mutation in mice eliminates the slow calcium current in skeletal muscle cells. Nature (Lond). 320:168-170.
5. Brandt, N.R., A.H. Caswell, S.R. Wen, and J.A. Talvenheimo. 1990. Molecular interactions of the junctional foot protein and dihydropyridine receptor in skeletal muscle triads. J. Membr. Biol. 113:237-251.
6. Caswell, A.M., N.R. Brandt, J.P. Brunschwig, and S, Purkerson. 1991. Localization and partial characterization of the oligomeric disulfide-linked molecular weight 95,000 protein (triadin) which binds the ryanodine and dihydropyridine receptors in skeletal muscle triadic vesicles. Biochemistry. 30:7507-7513.
7. Chaudhari, N. 1992. A single nucleotide deletion in the skeletal muscle-specific calcium channel transcript of muscular dysgenesis (mag) mice. J. Biol. Chem. 267:25636-25639.
8. Chaudhari, N., and K.G. Beam 1990. Fibroblasts fuse with myotubes developing in culture. Adv. Exp. Med. Biol. 280:131-136.
9. Chaudhari, N., and K.G. Beam. 1993. mRNA for cardiac calcium channel is expressed during development of skeletal muscle. Dev. Biol. 155:507-515.
10. Corbett, A.M., A.H. Caswell, N.R. Brandt, and J.-P. Brunschwig. 1985. Determinants of triad junction reformation: identification and isolation of an endogenous promoter for junction reformation in skeletal muscle. J. Membr. Biol. 86:267-276.
11. Courbin, P., J. Koenig, A. Ressouches, K.G. Beam, and J.A. Powell. 1989. Rescue of excitation-contraction coupling in dysgenic muscle by addition of fibroblasts in vitro. Neuron. 2:1341-1350.
12. Fleischer, S., and M. Inui. 1989. Biochemistry and biophysics of excitation-contraction coupling. Annu. Rev. Biophys. Biophys. Chem. 18:333-364.
13. Flucher, B.E. 1992. Structural analysis of muscle development: transverse tubules, sarcoplasmic reticulum, and the triad. Dev. Biol. 154:245-260.
14. 2. J. Cell Biol. 115:1345-1356.
15. Flucher, B.E., M, Terasaki, H. Chin, T. Beeler, and M.P. Daniels. 1991b. Biogenesis of transverse tubules in skeletal muscle in vitro. Dev. Biol. 145:77-90.
16. Flucher, B.E., S.B. Andrews, S. Fleischer, A.R. Marks, A. Caswell, and J.A. Powell. 1993. Triad formation: organization and function of the sarcoplasmic reticulum calcium release channel and triadin in normal and dysgenic muscle in vitro. J. Cell Biol. 123:1161-1174.
17. Flucher, B.E., S.B. Andrews, and M.P. Daniels. 1994. Molecular organization of T-tubule/SR junctions during development of excitation-contraction coupling in skeletal muscle. Mol. Biol. Cell. 5:1105-1118.
18. Franzini-Armstrong, C. 1970. Studies of the triad. I. Structure of the junction in frog twitch fibers. J. Cell Biol. 47:488-499.
19. Franzini-Armstrong, C., M. Pinçon-Raymond, and F. Rieger. 1991. Muscle fibers from dysgenic mouse in vivo lack a surface component of peripheral couplings. Dev. Biol. 146:364-376.
20. Garcia, L., M. Pinçon-Raymond, G. Romey, J.-P. Changeux, M. Lazdunski, and F. Rieger. 1990. Induction of normal ultrastructure by CGRP treatment in dysgenic myotubes. FEBS Lett. 263:147-152.
21. Graham, F.L., and A.J. Van der Eb. 1973. A new technique for the assay of infectivity of human adenovirus 5 DNA. Virology. 52:456-467.
22. Isom, L.L., K.S. DeJongh, and W. A. Catterall. 1994. Auxiliary subunits of voltage-gated ion channels. Neuron. 12:1183-1194.
23. 2+-release channel/ryanodine receptor is localized in junctional and corbular sarcoplasmic reticulum in cardiac muscle. J. Cell Biol. 120:969-980.
24. Junker, J., J.R. Sommer, M. Sar, and G. Meissner. 1994, Extended junctional sarcoplasmic reticulum of avian cardiac muscle contains functional ryanodine receptors. J. Biol. Chem. 269:1627-1634.
25. 2+-ATPase in developing chick skeletal muscle. Dev. Biol. 124:490-503.
26. Kim, K.C., A.M. Caswell, J.A. Talvenheimo, and N.R. Brandt. 1990a. Isolation of a terminal cisterna protein which may link the dihydropyridine receptor to the junctional foot protein in skeletal muscle. Biochemistry. 29:9281-9289.
27. Kim, K.C., A.H. Caswell, J.-P. Brunschwig, and N.R. Brandt. 1990b. Identification of a new subpopulation of triad junctions isolated from skeletal muscle: morphological correlations with intact muscle. J. Membr. Biol. 113:221-235.
28. 2+ in excitation-contraction uncoupled dysgenic muscle. Dev. Biol. 99:152-165.
29. 1 subunit of the dihydropyridine receptor in mice with muscular dysgenesis. J. Biol. Chem. 264:1345-1348.
30. Knudson, C.M., K.K. Stang, C.R. Moomaw, C.A. Slaughter, and K.P. Campbell. 1993. Primary structure and topological analysis of a skeletal muscle-specific junctional sarcoplasmic reticulum glycoprotein (triadin). J. Biol. Chem. 268:12646-12654.
31. Lau, Y.H., A.H. Caswell, and J.-P. Brunschwig. 1977. Isolation of transverse tubules by fractionation of triad junctions of skeletal muscle. J. Biol. Chem. 252:5565-5574.
32. Lu, X., L. Xu, and G. Meissner. 1994. Activation of the skeletal muscle calcium release channel by a cytoplasmic loop of the dihydropyridine receptor. J. Biol. Chem. 269:6511-6516.
33. Morton, M.E., and S.C. Froehner. 1987. Monoclonal antibody identifies a 200-kDa subunit of the dihydropyridine-sensitive calcium. J. Biol. Chem. 262: 11904-11907.
34. Morton, M.E., and S.C. Froehner. 1989. The alpha-1 and alpha-2 polypeptides of the dihydropyridine-sensitive calcium-channel differ in developmental expression and tissue distribution. Neuron. 2:1499-1506.
35. Pai, A.C. 1965. Developmental genetics of a lethal mutation, muscular dysgenesis (mdg) in the mouse. 1. Genetic analysis and gross morphology. Dev. Biol. 11:82-92.
36. Pinçon-Raymond, M., L. Garcia, G. Romey, L. Houenou, M. Lazdunski, and F. Rieger. 1990. A genetic model for the study of abnormal nerve-muscle interactions at the level of excitation-contraction coupling: the mutation muscular dysgenesis. J. Physiol. (Paris). 84:82-87.
37. Pinçon-Raymond, M., V. Vicart, P. Bois, O. Chassande, G. Romey, G. Varadi, Z.L. Li, M. Lazdunski, R. Rieger, and D. Paulin. 1991. Conditional immortalization of normal and dysgenic mouse muscle cells by the SV40 Large T antigen under the vimentin promoter control. Dev. Biol. 148:517-528.
38. Platzer, A. 1979. Embryology of two murine muscle diseases: muscular dystrophy and muscular dysgenesis. Ann. N. Y. Acad. Sci. 317:94-113.
39. Platzer, A.C., and S. Gluecksohn-Waelsch. 1972. Fine structure of mutant (muscular dysgenesis) embryonic mouse muscle. Dev. Biol. 28:242-252.
40. Powell, J.A. 1990. Muscular dysgenesis: a model system for studying skeletal muscle development. FASEB (Fed. Am. Soc. Exp. Biol.) J. 4:2798-2808.
41. Powell, J.A., and D.M. Fambrough. 1973. Electrical properties of normal and dysgenic mouse skeletal muscle in culture. J. Cell. Physiol. 82:21-38.
42. Rieger, F., M. Pinçon-Raymond, A.M. Tassin, L. Garcia, G. Romey, M. Fosset, and M. Lazdunski. 1987. Excitation-contraction uncoupling in the developing skeletal muscle of the muscular dysgenesis mouse embryo. Biochimie (Paris). 69:411-417.
43. Rios, E., J.J. Ma, and A. Gonzalez. 1991. The mechanical hypothesis of excitation-contraction (E-C) coupling in skeletal muscle. J. Muscle Res. Cell Motil. 12:127-135.
44. Stockdale, F.E., and H. Holtzer. 1961. DNA synthesis and myogenesis. Exp. Cell Res. 24:508-520.
45. Sun, X.-H., F. Protasi, M. Takahasi, H. Takeshima, D.G. Ferguson, and C. Franzini-Armstrong. 1995. Molecular architecture of membranes involved in excitation-contraction coupling of cardiac muscle. J. Cell Biol. 129:659-671.
46. Takekura, H., X.-H. Sun, and C. Franzini-Armstrong. 1994. Development of the excitation-contraction coupling apparatus in skeletal muscle: peripheral and internal calcium release units are formed sequentially. J. Muscle Res. Cell Motil. 15:102-118.
47. Takekura, H., M. Nishi, T. Noda, H. Takeshima, and C. Franzini-Armstrong. 1995. Abnormal junctions between surface membrane and sarcoplasmic reticulum in skeletal muscle with a mutation targeted to the ryanodine receptor. Proc. Natl. Acad. Sci. USA. 92:3381-3385.
48. Takeshima, H., S. Nishimura, T. Matsumoto, H. Ishida, K. Kangawa, N. Minamino, H. Matsuo, M. Ueda, M. Hanaoka, T. Hirose, et al. 1989. Primary structure and expression from complementary DNA of skeletal muscle ryanodine receptor. Nature (Lond.). 339:439-445.
49. Takeshima, H., M. Iino, H. Takekura, M. Nishi, J. Kuno, O. Minowa, H. Takano, and T. Noda. 1994. Excitation-contraction uncoupling and muscular degeneration in mice lacking functional skeletal muscle ryanodine-receptor gene. Nature (Lond.). 369:556-559.
50. Tanabe, T., B.A. Adams, S. Numa, and K.G. Beam. 1991. Repeat I of the dihydropyridine receptor is critical in determining calcium channel activation kinetics. Nature (Lond). 352:800-803.
51. 2+ channels do not overcome the E-C coupling defect in immortalized dysgenic muscle cells: evidence for a missing link. FEBS Lett. 368:405-410.
52. Wagenknecht, T., R. Grassucci, J. Frank, A. Saito, M. Inui, and S. Fleischer. 1989. Three-dimensional architecture of the calcium channel/foot structure of sarcoplasmic reticulum. Nature (Lond.). 338:167-170.
53. Yuan, S.H., W. Arnold, and A.O. Jorgensen. 1991. Biogenesis of transverse tubules and triads: immunolocalization of the 1,4-dihydropyridine receptor, TS28, and the ryanodine receptor in rabbit skeletal muscle developing in situ. J. Cell Biol. 112:289-301.