The calcium channel α2/δ1 subunit interacts with ATP5b in the plasma membrane of developing muscle cells

American Journal of Physiology - Cell Physiology

Volumn 301, Issue 1, 2011, Pages

  García, Jesús ^a  

^a UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

Author keywords

Signaling; Skeletal muscle

Indexed keywords

1,4 DIHYDROPYRIDINE RECEPTOR; CALCIUM CHANNEL; CALCIUM CHANNEL ALPHA2; CALCIUM CHANNEL DELTA1; CELL MEMBRANE PROTEIN; PROTEIN ATP5B; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; BINDING KINETICS; CELL MATURATION; CELL MEMBRANE; CELLULAR DISTRIBUTION; CONTROLLED STUDY; FLUORESCENCE RESONANCE ENERGY TRANSFER; IMMUNOPRECIPITATION; INTRACELLULAR MEMBRANE; MOUSE; MUSCLE CELL; MUSCLE DEVELOPMENT; MYOTUBE; NEWBORN; NONHUMAN; PRIORITY JOURNAL; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; SIGNAL TRANSDUCTION; SKELETAL MUSCLE;

ANIMALS; CALCIUM CHANNELS; CALCIUM CHANNELS, L-TYPE; CELL DIFFERENTIATION; CELL MEMBRANE; CELLS, CULTURED; FLUORESCENCE RESONANCE ENERGY TRANSFER; IMMUNOPRECIPITATION; MASS SPECTROMETRY; MEMBRANE POTENTIALS; MICE; MITOCHONDRIA, MUSCLE; MITOCHONDRIAL PROTON-TRANSLOCATING ATPASES; MUSCLE FIBERS, SKELETAL; SIGNAL TRANSDUCTION;

EID: 79959815647     PISSN: 03636143     EISSN: 15221563     Source Type: Journal    
DOI: 10.1152/ajpcell.00405.2010     Document Type: Article

References (42)

1. Araya R, Riquelme MA, Brandan E, Saez JC. The formation of skeletal muscle myotubes requires functional membrane receptors activated by extracellular ATP. Brain Res Rev 47: 174-188, 2004.
2. Bangalore R, Mehrke G, Gingrich K, Hofmann F, Kass RS. Influence of L-type Ca channel α2/δ1-subunit on ionic and gating current in transiently transfected HEK 293 cells. Am J Physiol Heart Circ Physiol 270: H1521-H1528, 1996.
3. Christopherson KS, Ullian EM, Stokes CC, Mullowney CE, Hell JW, Agah A, Lawler J, Mosher DF, Bornstein P, Barres BA. Thrombospondins are astrocyte-secreted proteins that promote CNS synaptogenesis. Cell 120: 421-433, 2005.
4. Cseri J, Szappanos H, Szigeti GP, Csernatony Z, Kovacs L, Csernoch L. A purinergic signal transduction pathway in mammalian skeletal muscle cells in culture. Pflügers Arch 443: 731-738, 2002.
5. + transporting ATP synthase on the surface of tumor cell lines. J Exp Med 180: 273-281, 1994.
6. Davies A, Douglas L, Hendrich J, Wratten J, Tran Van Minh A, Foucault I, Koch D, Pratt WS, Saibil HR, Dolphin AC. The calcium channel α2/δ-2 subunit partitions with CaV2.1 into lipid rafts in cerebellum: implications for localization and function. J Neurosci 26: 8748-8757, 2006.
7. Deli T, Szappanos H, Szigeti GP, Cseri J, Kovacs L, Csernoch L. Contribution from P2X and P2Y purinoceptors to ATP-evoked changes in intracellular calcium concentration on cultured myotubes. Pflügers Arch 453: 519-529, 2007.
8. Dolphin AC. Calcium channel diversity: multiple roles of calcium channel subunits. Current Opinion Neurobiology 19: 237-244, 2009.
9. Erickson MG, Moon DL, Yue DT. DsRed as a Potential FRET Partner with CFP and GFP. Biophys J 85: 599-611, 2003.
10. Eroglu C, Allen NJ, Susman MW, O'Rourke NA, Park CY, Ozkan E, Chakraborty C, Mulinyawe SB, Annis DS, Huberman AD, Green EM, Lawler J, Dolmetsch R, Garcia KC, Smith SJ, Luo D, Rosenthal A, Mosher DF, Barres BA. Gabapentin receptor α2/δ1 is a neuronal thrombospondin receptor responsible for excitatory CNS synaptogenesis. Cell 139: 380-392, 2009.
11. Flucher BE, Phillips JL, Powell JA. Dihydropyridine receptor α subunits in normal and dysgenic muscle in vitro: expression of α 1 is required for proper targeting and distribution of α 2. J Cell Biol 115: 1345-1356, 1991.
12. Forrester T, Hassan MO. Appearance of adenosine triphosphate in the perfusate from active frog skeletal muscle. J Physiol 232: 86P-88P, 1973.
13. Gach MP, Cherednichenko G, Haarmann C, Lopez JR, Beam KG, Pessah IN, Franzini-Armstrong C, Allen PD. α2/δ1 dihydropyridine receptor subunit is a critical element for excitation-coupled calcium entry but not for formation of tetrads in skeletal muscle. Biophys J 94: 3023-3034, 2008.
14. García J, Beam KG. Measurements of calcium transients and slow calcium current in myotubes. J Gen Physiol 103: 107-123, 1994.
15. Garcia K, Nabhani T, García J. The Calcium Channel α2/δ1 Subunit is Involved in Extracellular Signaling. J Physiol 586.3: 727-738, 2008.
16. Hosey MM, Barhanin J, Schmid A, Vandaele S, Ptasienski J, O'Callahan C, Cooper C, Lazdunski M. Photoaffinity labeling and phosphorylation of a 165 kilodalton peptide associated with dihydropyridine and phenylalkylamine-sensitive calcium channels. Biochem Biophys Res Commun 147: 1137-1145, 1987.
17. Huang TC, Chang HY, Hsu CH, Kuo WH, Chang KJ, Juan HF. Targeting therapy for breast carcinoma by ATP synthase inhibitor aurovertin B. J Proteome Res 7: 1433-1444, 2008.
18. Jay SD, Sharp AH, Kahl SD, Vedvick TS, Harpold MM, Campbell KP. Structural characterization of the dihydropyridine-sensitive calcium channel alpha 2-subunit and the associated delta peptides. J Biol Chem 266: 3287-3293, 1991.
19. Kaczmarek LK. Non-conducting functions of voltage-gated ion channels. Nat Rev Neurosci 7: 761-71, 2006.
20. 2+ channel from rabbit skeletal muscle. Evidence for two distinct high molecular weight subunits. J Biol Chem 262: 7943-7946, 1987.
21. Li J, King N, Sinoway LI. ATP concentrations and muscle tension increase linearly with muscle contraction. J Appl Physiol 95: 577-583, 2003.
22. Martinez LO, Jacquet S, Esteve JP, Rolland C, Cabezon E, Champagne E, Pineau T, Georgeaud V, Walker JE, Terce F, Collet X, Perret B, Barbaras R. Ectopic β-chain of ATP synthase is an apolipoprotein A-I receptor in hepatic HDL endocytosis. Nature 421: 75-79, 2003.
23. Morton M, Froehner S. Monoclonal antibody identifies a 200-kDa subunit of the dihydropyridine-sensitive calcium channel. Neuron 2: 1499-1506, 1989.
24. Moser TL, Stack MS, Asplin I, Enghild JJ, Hojrup P, Everitt L, Hubchak S, Schnaper HW, Pizzo SV. Angiostatin binds ATP synthase on the surface of human endothelial cells. Proc Natl Acad Sci USA 96: 2811-2816, 1999.
25. 2+ current kinetics in skeletal muscle but not targeting of α 1s or excitation-contraction coupling. J Biol Chem 280: 2229-2237, 2005.
26. Osanai T, Magota K, Tanaka M, Shimada M, Murakai R, Sasaki S, Tomita H, Maeda N, Okumura K. Intracellular signaling for vasoconstrictor coupling factor 6. Novel function of β-subunit of ATP synthase as receptor. Hypertension 46: 1140-1146, 2005.
27. Rigault C, Bernard A, Georges B, Kandel A, Pfutzner E, LeBorgne F, DemarquoyJ. Extracellular ATP increases L-carnitine transport and content in C2C12 cells. Pharmacology 81: 246-250, 2008.
28. Ryten M, Yang SY, Dunn PM, Goldspink G, Burnstock G. Purinoceptor expression in regenerating skeletal muscle in the mdx mouse model of muscular dystrophy and in satellite cell cultures. FASEB J 18: 1404-1406, 2004.
29. Sandona D, Danieli-Betto D, Germinario E, Biral D, Martinello T, Lioy A, Tarricone E, Gastaldello S, Betto R. The T-tubule membrane ATP-operated P2X4 receptor influences contractility of skeletal muscle. FASEB J 19: 1184-1186, 2005.
30. Shagger H, vonJagow G. Blue native electrophoresis for isolation of membrane protein complexes in enzymatically active form. Anal Biochem 199: 223-231, 1991.
31. Shirokov R, Ferreira G, Yi J, Ríos E. Inactivation of the gating currents of L-type calcium channels. Specific role of the 2α/δ subunit. J Gen Physiol 111: 807-823, 1998.
32. Sieber M, Nastainczyk W, Zubor V, Wernet W, Hofmann F. The 165-KDa peptide of the purified skeletal muscle dihydropyridine receptor contains the known regulatory sites of the calcium channel. Eur J Biochem 167: 117-122, 1987.
33. Silinsky EM. On the association between transmitter secretion and the release of adenine nucleotides from mammalian motor nerve terminals. J Physiol 247: 145-162, 1975.
34. Swamy M, Siegers GM, Minguet S, Wollscheid B, Schamel WWA. Blue native polyacrylamide gel electrophoresis (BN-PAGE) for the identification and analysis of multiprotein complexes (Abstract). Sci STKE 345: l4, 2006.
35. Szigeti GP, Szappanos H, Deli T, Cseri J, Kovacs L, Csernoch L. Differentiation-dependent alterations in the extracellular ATP-evoked calcium fluxes of cultured skeletal muscle cells from mice. Pflügers Arch 453: 509-518, 2007.
36. Takahashi M, Seagar MJ, Jones JF, Reber BF, Catterall WA. Subunit structure of dihydropyridine-sensitive calcium channels from skeletal muscle. Proc Natl Acad Sci USA 84: 5478-5482, 1987.
37. Vandaele SF, Rieger F. Co-localization of 1,4-dihydropyridine receptor α2/δ subunit and N-CAM during early myogenesis in vitro. J Cell Sci 107: 1217-1227, 1994.
38. Varadi G, Orlowski J, Schwartz A. Developmental regulation of expression of the alpha 1 and alpha 2 subunits mRNAs of the voltagedependent calcium channel in a differentiating myogenic cell line. FEBS Lett 250: 515-518, 1989.
39. Wang T, Chen Z, Wang X, Shyy JYJ, Zhu Y. Cholesterol loading increases the translocation of ATP synthaseβ chain into membrane caveolae in vascular endothelial cells. Biochim Biophys Acta 1761: 1182-1190, 2006.
40. Wittig I, Braun HP, Schagger H. Blue native PAGE. Nature Protocols 1: 418-428, 2006.
41. Yamamoto K, Shimizu N, Obi S, Kumagaya S, Taketani Y, Kamiya A, Ando J. Involvement of cell surface ATP synthase in flow-induced ATP release by vascular endothelial cells. Am J Physiol Heart Circ Physiol 293: H1646-H1653, 2007.
42. Yeung D, Zablocki K, Lien CF, Jiang T, Arkle S, Brutkowski W, Brown J, Lochmuller H, Simon J, Barnard EA, Gorecki DC. Increased susceptibility to ATP via alteration of P2X receptor function in dystrophic mdx mouse muscle cells. FASEB J 20: 610-620, 2006.