User menu

Essential role of TRPV2 ion channel in the sensitivity of dystrophic muscle to eccentric contractions.

Bibliographic reference Zanou, Nadège ; Iwata, Yuko ; Schakman, Olivier ; Lebacq, Jean ; Wakabayashi, Shigeo ; et. al. Essential role of TRPV2 ion channel in the sensitivity of dystrophic muscle to eccentric contractions.. In: FEBS Letters, Vol. 583, no. 22, p. 3600-3604 (2009)
Permanent URL
  1. Blake, Physiol. Rev., 82, 291 (2002)
  2. Gillis J. M., 10.1023/a:1005545325254
  3. Monaco Anthony P., Neve Rachael L., Colletti-Feener Chris, Bertelson Corlee J., Kurnit David M., Kunkel Louis M., Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene, 10.1038/323646a0
  4. Hoffman Eric P., Brown Robert H., Kunkel Louis M., Dystrophin: The protein product of the duchenne muscular dystrophy locus, 10.1016/0092-8674(87)90579-4
  5. Ervasti James M., Campbell Kevin P., Membrane organization of the dystrophin-glycoprotein complex, 10.1016/0092-8674(91)90035-w
  6. Culligan, Int. J. Mol. Med., 2, 639 (1998)
  7. Ervasti J. M., A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin, 10.1083/jcb.122.4.809
  8. Carlson C. George, Acetylcholine receptor and calcium leakage activity in nondystrophic and dystrophic myotubes (MDX), 10.1002/(sici)1097-4598(199610)19:10<1258::aid-mus3>;2-d
  9. Haws C. M., Lansman J. B., Developmental Regulation of Mechanosensitive Calcium Channels in Skeletal Muscle from Normal and mdx Mice, 10.1098/rspb.1991.0105
  10. Franco Alfredo, Lansman Jeffry B., Calcium entry through stretch-inactivated ion channels in mdx myotubes, 10.1038/344670a0
  11. Franco-Obregon, J. Physiol., 481, 299 (1994)
  12. Ruegg Urs T, Gillis Jean-Marie, Calcium homeostasis in dystrophic muscle, 10.1016/s0165-6147(99)01377-2
  13. Gailly, Biochim. Biophys. Acta, 1600, 38 (2002)
  14. Turner Paul R., Westwood Tim, Regen Chester M., Steinhardt Richard A., Increased protein degradation results from elevated free calcium levels found in muscle from mdx mice, 10.1038/335735a0
  15. Badalamente Marie A., Stracher Alfred, Delay of muscle degeneration and necrosis in mdx mice by calpain inhibition, 10.1002/(sici)1097-4598(200001)23:1<106::aid-mus14>;2-d
  16. Gailly P., De Backer F., Van Schoor M., Gillis J. M., In situmeasurements of calpain activity in isolated muscle fibres from normal and dystrophin-lackingmdxmice : Calpain activity in single muscle fibres, normal and dystrophic, 10.1113/jphysiol.2007.132191
  17. Iyer Sushella L., Katyare S.S., Howland J.L., Elevated erythrocyte phospholipase A associated with Duchenne and myotonic muscular dystrophy, 10.1016/0304-3940(76)90032-x
  18. Boittin F.-X., Ca2+-independent phospholipase A2 enhances store-operated Ca2+ entry in dystrophic skeletal muscle fibers, 10.1242/jcs.03184
  19. Vandebrouck, FASEB J., 20, 136 (2006)
  20. Ragusa Robert J., Chow Ching K., Porter John D., Oxidative stress as a potential pathogenic mechanism in an animal model of Duchenne muscular dystrophy, 10.1016/s0960-8966(97)00096-5
  21. Shkryl Vyacheslav M., Martins Adriano S., Ullrich Nina D., Nowycky Martha C., Niggli Ernst, Shirokova Natalia, Reciprocal amplification of ROS and Ca2+ signals in stressed mdx dystrophic skeletal muscle fibers, 10.1007/s00424-009-0670-2
  22. Iwata, Hum. Mol. Genet., 18, 824 (2009)
  23. Damann Nils, Voets Thomas, Nilius Bernd, TRPs in Our Senses, 10.1016/j.cub.2008.07.063
  24. Muraki Katsuhiko, Iwata Yuko, Katanosaka Yuki, Ito Tomohiro, Ohya Susumu, Shigekawa Munekazu, Imaizumi Yuji, TRPV2 Is a Component of Osmotically Sensitive Cation Channels in Murine Aortic Myocytes, 10.1161/01.res.0000097263.10220.0c
  25. Iwata Yuko, Katanosaka Yuki, Arai Yuji, Komamura Kazuo, Miyatake Kunio, Shigekawa Munekazu, A novel mechanism of myocyte degeneration involving the Ca2+-permeable growth factor–regulated channel, 10.1083/jcb.200301101
  26. Moens P., Baatsen P. H. W. W., Mar�chal G., Increased susceptibility of EDL muscles from mdx mice to damage induced by contractions with stretch, 10.1007/bf00121296
  27. Brooks, J. Physiol., 404, 71 (1988)
  28. Bansal Dimple, Miyake Katsuya, Vogel Steven S., Groh Séverine, Chen Chien-Chang, Williamson Roger, McNeil Paul L., Campbell Kevin P., Defective membrane repair in dysferlin-deficient muscular dystrophy, 10.1038/nature01573
  29. Suchyna Thomas M., Johnson Janice H., Hamer Katherine, Leykam Joseph F., Gage Douglas A., Clemo Henry F., Baumgarten Clive M., Sachs Frederick, Identification of a Peptide Toxin fromGrammostola spatulataSpider Venom That Blocks Cation-Selective Stretch-Activated Channels, 10.1085/jgp.115.5.583
  30. Vandebrouck Clarisse, Martin Dominique, Schoor Monique Colson-Van, Debaix Huguette, Gailly Philippe, Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers, 10.1083/jcb.200203091
  31. Ducret Thomas, Vandebrouck Clarisse, Cao My Linh, Lebacq Jean, Gailly Philippe, Functional role of store-operated and stretch-activated channels in murine adult skeletal muscle fibres : Store-operated and stretch-activated channels in skeletal muscle fibres, 10.1113/jphysiol.2006.115154
  32. Suchyna Thomas M., Sachs Frederick, Mechanosensitive channel properties and membrane mechanics in mouse dystrophic myotubes : Mechanosensitive channel properties and membrane mechanics, 10.1113/jphysiol.2006.125021
  33. Putney, Mol. Interventions, 1, 84 (2001)
  34. Yeung Ella W., Whitehead Nicholas P., Suchyna Thomas M., Gottlieb Philip A., Sachs Frederick, Allen David G., Effects of stretch-activated channel blockers on [Ca2+]iand muscle damage in themdxmouse : Stretch-induced damage inmdxmuscle fibres, 10.1113/jphysiol.2004.075275
  35. Lynch Gordon S., Hinkle Richard T., Chamberlain Jeffrey S., Brooks Susan V., Faulkner John A., Force and power output of fast and slow skeletal muscles frommdxmice 6-28 months old, 10.1111/j.1469-7793.2001.00591.x
  36. Imbert Nathalie, Vandebrouck Clarissre, Constantin Bruno, Duport Gérard, Guillou Claire, Cognard Christian, Raymond Guy, Hypoosmotic shocks induce elevation of resting calcium level in duchenne muscular dystrophy myotubes contracting in vitro, 10.1016/0960-8966(96)00351-3
  37. Tutdibi O., Brinkmeier H., Rüdel R., Föhr K. J., Increased calcium entry into dystrophin-deficient muscle fibres of MDX and ADR-MDX mice is reduced by ion channel blockers, 10.1111/j.1469-7793.1999.859ab.x
  38. Mallouk, Am. J. Physiol. Cell Physiol., 278, C473 (2000)
  39. Gailly Ph., Boland B., Himpens B., Casteels R., Gillis J.M., Critical evaluation of cytosolic calcium determination in resting muscle fibres from normal and dystrophic (mdx) mice, 10.1016/0143-4160(93)90006-r
  40. Gailly Ph., Hermans E., Octave J.N., Gillis J.M., Specific increase of genetic expression of parvalbumin in fast skeletal muscles of mdx mice, 10.1016/0014-5793(93)81806-b
  41. Imbert Nathalie, Vandebrouck Clarisse, Duport Gérard, Raymond Guy, Hassoni Abdul A., Constantin Bruno, Cullen Michael J., Cognard Christian, Calcium currents and transients in co-cultured contracting normal and Duchenne muscular dystrophy human myotubes, 10.1111/j.1469-7793.2001.00343.x
  42. Rolland Jean-François, De Luca Annamaria, Burdi Rosa, Andreetta Francesca, Confalonieri Paolo, Conte Camerino Diana, Overactivity of exercise-sensitive cation channels and their impaired modulation by IGF-1 in mdx native muscle fibers: Beneficial effect of pentoxifylline, 10.1016/j.nbd.2006.08.010
  43. Kojima Itaru, Kanzaki Makoto, Zhang* You-Qing, Mashima* Hirosato, Li* Lu, Shibata* Hiroshi, 10.1038/11086
  44. KOWASE TAKANORI, NAKAZATO YOICHI, YOKO-O HIDEAKI, MORIKAWA AKIHIRO, KOJIMA ITARU, Immunohistochemical Localization of Growth Factor-Regulated Channel (GRC) in Human Tissues., 10.1507/endocrj.49.349
  45. Petrof B. J., Shrager J. B., Stedman H. H., Kelly A. M., Sweeney H. L., Dystrophin protects the sarcolemma from stresses developed during muscle contraction., 10.1073/pnas.90.8.3710
  46. Lynch, Am. J. Physiol. Cell Physiol., 279, C1290 (2000)
  47. Deconinck N., Rafael J.A., Beckers-Bleukx G., Kahn D., Deconinck A.E., Davies K.E., Gillis J.M., Consequences of the combined deficiency in dystrophin and utrophin on the mechanical properties and myosin composition of some limb and respiratory muscles of the mouse, 10.1016/s0960-8966(98)00048-0
  48. Law Douglas J., Tidball James G., Caputo Angelo, Site and mechanics of failure in normal and dystrophin-deficient skeletal muscle, 10.1002/mus.880180211
  49. Yeung E. W., Gadolinium reduces short-term stretch-induced muscle damage in isolated mdx mouse muscle fibres, 10.1113/jphysiol.2003.047373
  50. Yeung, J. Appl. Physiol., 94, 2475 (2003)
  51. Zhang B.-T., Yeung S. S., Allen D. G., Qin L., Yeung E. W., Role of the calcium-calpain pathway in cytoskeletal damage after eccentric contractions, 10.1152/japplphysiol.90320.2008