Reduced expression and abnormal localization of the KATP channel subunit SUR2A in patients with familial hypokalemic periodic paralysis

Biochemical and Biophysical Research Communications

Volumn 391, Issue 1, 2010, Pages 974-978

  Kim, Sung Jo ^a   Lee, Yea Jin ^a   Kim, June Bum ^b  

^a Hoseo University   (South Korea)

^b Konyang University College of Medicine   (South Korea)

Author keywords

Depolarization; Hypokalemic periodic paralysis; Potassium channel; Sulfonylurea receptor

Indexed keywords

ADENOSINE TRIPHOSPHATE SENSITIVE POTASSIUM CHANNEL; MESSENGER RNA; POTASSIUM; SUR2A PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; CELL CULTURE; CELL LEVEL; CHANNEL GATING; CONTROLLED STUDY; CULTURE MEDIUM; CYTOSOLIC FRACTION; DEPOLARIZATION; GASTROCNEMIUS MUSCLE; GENE EXPRESSION REGULATION; GENE LOCATION; HUMAN; HUMAN CELL; MOLECULAR DYNAMICS; MUSCLE CELL; PERIODIC PARALYSIS; PRIORITY JOURNAL; PROTEIN CONTENT; PROTEIN EXPRESSION; PROTEIN LOCALIZATION;

ATP-BINDING CASSETTE TRANSPORTERS; CYTOSOL; HUMANS; HYPOKALEMIC PERIODIC PARALYSIS; MUSCLE, SKELETAL; POTASSIUM CHANNELS, INWARDLY RECTIFYING; RECEPTORS, DRUG; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER;

EID: 73149114379     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2009.11.177     Document Type: Article

References (27)

1. Kim J.B., Kim M.H., Lee S.J., Kim D.J., and Lee B.C. The genotype and clinical phenotype of Korean patients with familial hypokalemic periodic paralysis. J. Korean Med. Sci. 22 (2007) 946-951
2. Venance S.L., Cannon S.C., Fialho D., Fontaine B., Hanna M.G., Ptacek L.J., Tristani-Firouzi M., Tawil R., and Griggs R.C. The primary periodic paralyses: diagnosis, pathogenesis and treatment. Brain 129 (2006) 8-17
3. Cannon S.C. Pathomechanisms in channelopathies of skeletal muscle and brain. Annu. Rev. Neurosci. 29 (2006) 387-415
4. Gennari F.J. Disorders of potassium homeostasis: hypokalemia and hyperkalemia. Crit. Care Clin. 18 (2002) 273-288
5. Noma A. ATP-regulated K+ channels in cardiac muscle. Nature 305 (1983) 147-148
6. Raab-Graham K.F., Radeke C.M., and Vandenberg C.A. Molecular cloning and expression of a human heart inward rectifier potassium channel. Neuroreport 5 (1994) 2501-2505
7. Spruce A.E., Standen N.B., and Stanfield P.R. Voltage-dependent ATP-sensitive potassium channels of skeletal muscle membrane. Nature 316 (1985) 736-738
8. Inagaki N., Gonoi T., Clement J.P., Namba N., Inazawa J., Gonzalez G., Aguilar-Bryan L., Seino S., and Bryan J. Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor. Science 270 (1995) 1166-1170
9. Seino S. ATP-sensitive potassium channels: a model of heteromultimeric potassium channel/receptor assemblies. Annu. Rev. Physiol. 61 (1999) 337-362
10. Matsuo M., Tanabe K., Kioka N., Amachi T., and Ueda K. Different binding properties and affinities for ATP and ADP among sulfonylurea receptor subtypes, SUR1, SUR2A, and SUR2B. J. Biol. Chem. 275 (2000) 28757-28763
11. Vanoye C.G., MacGregor G.G., Dong K., Tang L., Buschmann A.S., Hall A.E., Lu M., Giebisch G., and Hebert S.C. The carboxyl termini of K(ATP) channels bind nucleotides. J. Biol. Chem. 277 (2002) 23260-23270
12. + channels. Neuron 16 (1996) 1011-1017
13. Ashcroft F.M., and Rorsman P. Electrophysiology of the pancreatic beta-cell. Prog. Biophys. Mol. Biol. 54 (1989) 87-143
14. + channels. Br. J. Pharmacol. 101 (1990) 531-540
15. ATP channels and basal coronary vascular tone. Cardiovasc. Res. 28 (1994) 811-817
16. Nichols C.G., and Lederer W.J. Adenosine triphosphate-sensitive potassium channels in the cardiovascular system. Am. J. Physiol. 261 (1991) H1675-H1686
17. Quayle J.M., Nelson M.T., and Standen N.B. ATP-sensitive and inwardly rectifying potassium channels in smooth muscle. Physiol. Rev. 77 (1997) 1165-1232
18. + depleted rat, an animal model of hypokalemic periodic paralysis. Mol. Pharmacol. 54 (1998) 197-206
19. + channels in patients with hypokalemic periodic paralysis. J. Clin. Invest. 103 (1999) 675-682
20. ATP deficiency in K+ depleted rats. Neuromuscul. Disord. 18 (2008) 74-80
21. Cottle D.L., McGrath M.J., Cowling B.S., Coghill I.D., Brown S., and Mitchell C.A. FHL3 binds MyoD and negatively regulates myotube formation. J. Cell Sci. 120 (2007) 1423-1435
22. Poole R.J., Briskin D.P., Kratky Z., and Johnstone R.M. Density gradient localization of plasma membrane and tonoplast from storage tissue of growing and dormant red beet: characterization of proton-transport and ATPase in tonoplast vesicles. Plant Physiol. 74 (1984) 549-556
23. Prinetti A., Chigorno V., Tettamanti G., and Sonnino S. Sphingolipid-enriched membrane domains from rat cerebellar granule cells differentiated in culture. A compositional study. J. Biol. Chem. 275 (2000) 11658-11665
24. Lapie P., Lory P., and Fontaine B. Hypokalemic periodic paralysis: an autosomal dominant muscle disorder caused by mutations in a voltage-gated calcium channel. Neuromusc. Disord. 7 (1997) 234-240
25. T.H. Kil, J.B. Kim, Severe respiratory phenotype caused by a de novo Arg528Gly mutation in the CACNA1S gene in a patient with hypokalemic periodic paralysis, Eur. J. Paediatr. Neurol. (2009), doi:10.1016/j.ejpn.2009.08.004, PMID: 19822448 (Epub ahead of print).
26. Kim J.B., Lee K.Y., and Hur J.K. A Korean family of hypokalemic periodic paralysis with mutation in a voltage-gated calcium channel (R1239G). J. Korean Med. Sci. 20 (2005) 162-165
27. Wang W., Jiang L., Ye L., Zhu N., Su T., Guan L., Li X., and Ning G. Mutation screening in Chinese hypokalemic periodic paralysis patients. Mol. Genet. Metab. 87 (2006) 359-363