Skeletal muscle store-operated channels and Ca2+ handling in muscular dystrophy

Store-operated Ca2+ entry (SOCE) pathways: Emerging signaling concepts in human (patho)physiology

Volumn , Issue , 2012, Pages 449-460

  Ruegg, Urs T ^a   Shapovalov, George ^a   Jacobson, Karin ^a   Reutenauer Patte, Julie ^a   Ismail, Hesham ^a   Dorchies, Olivier M ^a   Avdonin, Pavel ^a  

^a UNIVERSITY OF GENEVA   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84930607375     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1007/978-3-7091-0962-5_28     Document Type: Chapter

References (73)

1. Alexander SPH, Mathie A, Peters JA (2005) Guide to receptors and channels: Ion channels. Br J Pharmacol 144(S1):73-94
2. Allard B (2006) Sarcolemmal ion channels in dystrophin-deficient skeletal muscle fibres. J Muscle Res Cell Motil 27(5):367-373
3. Allen D, Gervasio O, Yeung E, Whitehead N (2010) Calcium and the damage pathways in muscular dystrophy. Can J Physiol Pharmacol 88(2):83-91
4. Allen DG, Whitehead NP (2011) Duchenne muscular dystrophy -what causes the increased membrane permeability in skeletal muscle? Int J Biochem Cell Biol 43(3):290-294
5. 2+ exchange in intact single skeletal muscle fibers from the mouse. Am J Physiol Cell Physiol 274(4):C940-C946
6. Basset O, Boittin F, Dorchies OM, Chatton JY, van Breemen C, Ruegg UT (2004) Involvement of inositol 1,4,5-trisphosphate in nicotinic calcium responses in dystrophic myotubes assessed by near-plasma membrane calcium measurement. J Biol Chem 279(45):47092-47100
7. Beech DJ, Bahnasi YM, Dedman AM, Al-Shawaf E (2009) TRPC channel lipid specificity and mechanisms of lipid regulation. Cell Calcium 45(6):583-588
8. Berbey C, Weiss N, Legrand C, Allard B (2009) Transient receptor potential canonical type 1 (TRPC1) operates as a sarcoplasmic reticulum calcium leak channel in skeletal muscle. J Biol Chem 284(52):36387-36394
9. Blake DJ, Weir A, Newey SE, Davies KE (2002) Function and genetics of dystrophin and dystrophin-related proteins in muscle. Physiol Rev 82(2):291-329
10. 2+ entry in dystrophic skeletal muscle fibers. J Cell Sci 119(18):3733-3742
11. Brooke MH, Fenichel GM, Griggs RC, Mendell JR, Miller P, Moxley R (1984) A trial of nifedipine in Duchenne muscular dystrophy. Neurology 34:290
12. Buetler TM, Renard M, Offord EA, Schneider H, Ruegg UT (2002) Green tea extract decreases muscle necrosis in mdx mice and protects against reactive oxygen species. Am J Clin Nutr 75 (4):749-753
13. Constantin B, Sebille S, Cognard C (2006) New insights in the regulation of calcium transfers by muscle dystrophin-based cytoskeleton: implications in DMD. J Muscle Res Cell Motil 27 (5):375-386
14. De Luca A, Pierno S, Liantonio A, Cetrone M, Camerino C, Simonetti S, Papadia F, Camerino DC (2001) Alteration of excitation-contraction coupling mechanism in extensor digitorum longus muscle fibres of dystrophic mdx mouse and potential efficacy of taurine. Br J Pharmacol 132 (5):1047-1054
15. Dietrich A, Chubanov V, Kalwa H, Rost BR, Gudermann T (2006) Cation channels of the transient receptor potential superfamily: their role in physiological and pathophysiological processes of smooth muscle cells. Pharmacol Ther 112(3):744-760
16. 2+ entry in dystrophic mdx mouse muscle. Am J Physiol Cell Physiol 299(1):C42-C50
17. 2+ influx into dystrophic mdx cardiomyocytes. Cell Calcium 46 (2):114-121
18. Gailly P (2002) New aspects of calcium signaling in skeletal muscle cells: implications in Duchenne muscular dystrophy. Biochim Biophys Acta 1600(1-2):38-44
19. Gailly P, Boland B, Himpens B, Casteels R, Gillis JM (1993) Critical evaluation of cytosolic calcium determination in resting muscle fibres from normal and dystrophic (mdx) mice. Cell Calcium 14:473-483
20. Gervasio OL, Whitehead NP, Yeung EW, Phillips WD, Allen DG (2008) TRPC1 binds to caveolin-3 and is regulated by Src kinase -role in Duchenne muscular dystrophy. J Cell Sci 121(13):2246-2255
21. Gottlieb P, Folgering J, Maroto R, Raso A, Wood TG, Kurosky A, Bowman C, Bichet D, Patel A, Sachs F, Martinac B, Hamill OP, Honore E (2008) Revisiting TRPC1 and TRPC6 mechanosensitivity. Pflügers Archiv Eur J Physiol 455(6):1097-1103
22. He L-P, Hewavitharana T, Soboloff J, Spassova MA, Gill DL (2005) A Functional link between store-operated and TRPC channels revealed by the 3,5-bis(trifluoromethyl)pyrazole derivative, BTP2. J Biol Chem 280(12):10997-11006
23. Hidalgo C, Sanchez G, Barrientos G, Aracena-Parks P (2006) A transverse tubule NADPH oxidase activity stimulates calcium release from isolated triads via ryanodine receptor type 1 S -glutathionylation. J Biol Chem 281(36):26473-26482
24. Hoffman EP, Brown RHJ, Kunkel LM (1987) Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell 51:919-928
25. Hotchkiss RS, Karl IE (1994) Dantrolene ameliorates the metabolic hallmarks of sepsis in rats and improves survival in a mouse model of endotoxemia. Proc Natl Acad Sci USA 91 (8):3039-3043
26. Imbert N, Cognard C, Duport G, Guillou C, Raymond G (1995) Abnormal calcium homeostasis in Duchenne muscular dystrophy myotubes contracting in vitro. Cell Calcium 18(3):177-186
27. Iwata Y, Katanosaka Y, Arai Y, Komamura K, Miyatake K, Shigekawa M (2003) A novel mechanism of myocyte degeneration involving the Ca2+-permeable growth factor-regulated channel. J Cell Biol 161(5):957-967
28. 2+ influx via TRPV2 ameliorates muscular dystrophy in animal models. Hum Mol Genet 18(5):824-834
29. 2+ signalling and reactive oxygen species-generating pathways. Cardiovasc Res 77(4):766-773
30. Kamkin A, Kiseleva I, Wagner K, Bohm J, Theres H, Günther J, Scholz H (2003) Characterization of stretch-activated ion currents in isolated atrial myocytes from human hearts. Pflügers Archiv Eur J Physiol 446(3):339-346
31. Khurana TS, Prendergast RA, Alameddine HS, Tome FM, Fardeau M, Arahata K, Sugita H, Kunkel LM (1995) Absence of extraocular muscle pathology in Duchenne's muscular dystrophy: role for calcium homeostasis in extraocular muscle sparing. J Exp Med 182(2):467-475
32. Leijendekker WJ, Passaquin AC, Metzinger L, Ruegg UT (1996) Regulation of cytosolic calcium in skeletal muscle cells of the mdx mouse under conditions of stress. Br J Pharmacol 118 (3):611-616
33. Lindahl M, Backman E, Henriksson KG, Gorospe JR, Hoffman EP (1995) Phospholipase A2 activity in dystrophinopathies. Neuromuscul Disord 5(3):193-199
34. 2+ cycling and new therapeutic approaches for heart failure. Circulation 121(6):822-830
35. 2+ in mdx mouse skeletal muscle fibers detected with Ca2+-activated K+ channels. Proc Natl Acad Sci USA 97(9):4950-4955
36. Maroto R, Raso A, Wood TG, Kurosky A, Martinac B, Hamill OP (2005) TRPC1 forms the stretch-activated cation channel in vertebrate cells. Nat Cell Biol 7(2):179-185
37. Marx SO, Ondrias K, Marks AR (1998) Coupled gating between individual skeletal muscle Ca2+ release channels (ryanodine receptors). Science 281(5378):818-821
38. Millay DP, Goonasekera SA, Sargent MA, Maillet M, Aronow BJ, Molkentin JD (2009) Calcium influx is sufficient to induce muscular dystrophy through a TRPC-dependent mechanism. Proc Natl Acad Sci USA 106(45):19023-19028
39. Monet M, Gkika D, Lehen'kyi V, Pourtier A, Vanden Abeele F, Bidaux G, Juvin V, Rassendren F, Humez S, Prevarsakaya N (2009) Lysophospholipids stimulate prostate cancer cell migration via TRPV2 channel stimulation. Biochim Biophys Acta 1793(3):528-539
40. Moxley RT, Brooke MH, Fenichel GM, Mendell JR, Griggs RC, Miller JP, Province MA, Patterson V (1987) Clinical investigation in Duchenne dystrophy. VI. Double-blind controlled trial of nifedipine. Muscle Nerve 10:22-33
41. Muraki K, Iwata Y, Katanosaka Y, Ito T, Ohya S, Shigekawa M, Imaizumi Y (2003) TRPV2 is a component of osmotically sensitive cation channels in murine aortic myocytes. Circ Res 93(9):829-838
42. Nakamura TY, Iwata Y, Sampaolesi M, Hanada H, Saito N, Artman M, Coetzee WA, Shigekawa M (2001) Stretch-activated cation channels in skeletal muscle myotubes from sarcoglycandeficient hamsters. Am J Physiol Cell Physiol 281(2):C690-C699
43. Nilius B, Owsianik G, Voets T, Peters JA (2007) Transient receptor potential cation channels in disease. Physiol Rev 87(1):165-217
44. Orlandi V, Campieri C, Mosconi G, D'Arcangelo GL, Feliciangeli G, Scolari MP, Stefoni S (2004) Tacrolimus-associated myositis: a case report in a renal transplant patient. Transplant Proc 36 (3):708-710
45. Passaquin A, Renard M, Kay L, Challet C, Mokhtarian A, Wallimann T, Ruegg UT (2002) Creatine supplementation reduces skeletal muscle degeneration and enhances mitochondrial function in mdx mice. Neuromuscul Disord 12(2):174-182
46. Poteser M, Graziani A, Rosker C, Eder P, Derler I, Kahr H, Zhu MX, Romanin C, Groschner K (2006) TRPC3 and TRPC4 associate to form a redox-sensitive cation channel: evidence for expression of native trpc3-trpc4 heteromeric channels in endothelial cells. J Biol Chem 281 (19):13588-13595
47. Pressmar J, Brinkmeier H, Seewald MJ, Naumann T, Rudel R (1994) Intracellular Ca2+ concentrations are not elevated in resting cultured muscle from Duchenne (DMD) patients and in mdx mouse muscle fibres. Pflugers Arch 426(6):499-505
48. 2+ handling and survival in mdx skeletal muscle cells. FEBS Lett 439(3):357-362
49. Putney JW (2010) Pharmacology of store-operated calcium channels. Mol Interv 10(4):209-218
50. Rando TA (2002) Oxidative stress and the pathogenesis of muscular dystrophies. Am J Phys Med Rehabil 81(11 Suppl):S175-S186
51. Rando TA, Disatnik M-H, Yu Y, Franco A (1998) Muscle cells from mdx mice have an increased susceptibility to oxidative stress. Neuromuscul Disord 8(1):14-21
52. Robert V, Massimino ML, Tosello V, Marsault R, Cantini M, Sorrentino V, Pozzan T (2001) Alteration in calcium handling at the subcellular level in mdx myotubes. J Biol Chem 276 (7):4647-4651
53. Ruegg UT, Gillis J-M (1999) Calcium homeostasis in dystrophic muscle. Trends Pharmacol Sci 20 (9):351-352
54. Sharif-Naeini R, Dedman A, Folgering J, Duprat F, Patel A, Nilius B, Honore E (2008) TRP channels and mechanosensory transduction: insights into the arterial myogenic response. Pflügers Archiv Eur J Physiol 456(3):529-540
55. 2+ signals in stressed mdx dystrophic skeletal muscle fibers. Pflugers Arch 458(5):915-928
56. Shou W, Aghdasi B, Armstrong DL, Guo Q, Bao S, Charng MJ, Mathews LM, Schneider MD, Hamilton SL, Matzuk MM (1998) Cardiac defects and altered ryanodine receptor function in mice lacking FKBP12. Nature 391(6666):489-492
57. Singaravelu K, Lohr C, Deitmer JW (2006) Regulation of store-operated calcium entry by calciumindependent phospholipase A2 in rat cerebellar astrocytes. J Neurosci 26(37):9579-9592
58. Smani T, Zakharov SI, Csutora P, Leno E, Trepakova ES, Bolotina VM (2004) A novel mechanism for the store-operated calcium influx pathway. Nat Cell Biol 6(2):113-120
59. Spurney CF, Knoblach S, Pistilli EE, Nagaraju K, Martin GR, Hoffman EP (2008) Dystrophindeficient cardiomyopathy in mouse: expression of Nox4 and Lox are associated with fibrosis and altered functional parameters in the heart. Neuromuscul Disord 18(5):371-381
60. Turner PR, Fong PY, Denetclaw WF, Steinhardt RA (1991) Increased calcium influx in dystrophic muscle. J Cell Biol 115:1701-1712
61. Turner PR, Westwood T, Regen CM, Steinhardt RA (1988) Increased protein degradation results from elevated free calcium levels found in muscle from mdx mice. Nature 335:735-738
62. Tutdibi O, Brinkmeier H, Rudel R, Fohr KJ (1999) Increased calcium entry into dystrophindeficient muscle fibres of MDX and ADR-MDX mice is reduced by ion channel blockers. J Physiol 515(3):859-868
63. 2+ channels with different activation modes and molecular origin in LNCaP human prostate cancer epithelial cells. J Biol Chem 279 (29):30326-30337
64. Vig M, DeHaven WI, Bird GS, Billingsley JM, Wang H, Rao PE, Hutchings AB, Jouvin M-H, Putney JW, Kinet J-P (2008) Defective mast cell effector functions in mice lacking the CRACM1 pore subunit of store-operated calcium release-activated calcium channels. Nat Immunol 9(1):89-96
65. Wehrens XHT, Lehnart SE, Reiken S, van der Nagel R, Morales R, Sun J, Cheng Z, Deng S-X, de Windt LJ, Landry DW, Marks AR (2005) Enhancing calstabin binding to ryanodine receptors improves cardiac and skeletal muscle function in heart failure. Proc Natl Acad Sci USA 102(27):9607-9612
66. Wehrens XHT, Marks AR (2004) Novel therapeutic approaches for heart failure by normalizing calcium cycling. Nat Rev Drug Discov 3(7):565-574
67. Whitehead NP, Streamer M, Lusambili LI, Sachs F, Allen DG (2006) Streptomycin reduces stretch-induced membrane permeability in muscles from mdx mice. Neuromuscul Disord 16(12):845-854
68. Winstead MV, Balsinde J, Dennis EA (2000) Calcium-independent phospholipase A2: structure and function. Biochim Biophys Acta 1488(1-2):28-39
69. Yano M, Kobayashi S, Kohno M, Doi M, Tokuhisa T, Okuda S, Suetsugu M, Hisaoka T, Obayashi M, Ohkusa T, Matsuzaki M (2003) FKBP12.6-mediated stabilization of calcium-release channel (ryanodine receptor) as a novel therapeutic strategy against heart failure. Circulation 107(3):477-484
70. Yeung EW, Whitehead NP, Suchyna TM, Gottleib PA, Sachs F, Allen DG (2005) Effects of stretch-activated channel blockers on [Ca2+]i and muscle damage in the mdx mouse. J Physiol 562(2):367-380
71. Zanou N, Iwata Y, Schakman O, Lebacq J, Wakabayashi S, Gailly P (2009) Essential role of TRPV2 ion channel in the sensitivity of dystrophic muscle to eccentric contractions. FEBS Lett 583(22):3600-3604
72. Zanou N, Shapovalov G, Louis M, Tajeddine N, Gallo C, Van Schoor M, Anguish I, Cao ML, Schakman O, Dietrich A, Lebacq J, Ruegg U, Roulet E, Birnbaumer L, Gailly P (2010) Role of TRPC1 channel in skeletal muscle function. Am J Physiol Cell Physiol 298(1):C149-C162
73. 2+ channels and T-lymphocyte activation by the pyrazole derivative BTP2. J Biol Chem 279(13):12427-12437