KATP channels: From structure to disease

Biologicheskie Membrany

Volumn 23, Issue 2, 2006, Pages 101-110

  Nichols, C G ^a   Koster, J ^a   Enkvetchakul, D ^a   Flagg, T ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 33845428562     PISSN: 02334755     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (73)

1. ATP: an inward rectifier subunit plus the sulfonylurea receptor // Science. 1995. V. 270 (5239). P. 1166-1170.
2. ATP channel complex // J. Gen. Physiol. 1997. V. 110 (6). P. 655-664.
3. + channels in the absence of the sulphonylurea receptor // Nature. 1997. V. 387 (6629). P. 179-183.
4. Nichols C.G., Shyng S.L., Nestorowicz A., Glaser B., Clement J.P., Gonzalez G., Aguilarbryan L., Permutt M.A., Bryan J. Adenosine diphosphate as an intracellular regulator of insulin secretion // Science. 1996. V. 272 (5269). P. 1785-1787
5. Nishida M., MacKinnon R. Structural basis of inward rectification. Cytoplasmic pore of the G protein-gated inward rectifier GIRK1 at 1.8A resolution // Cell. 2002. V. 111 (7). P. 957-965.
6. Pegan S., Arrabit C., Zhou W., Kwiatkowski W., Collins A., Slesinger P.A., Choe S. Cytoplasmic domain structures of Kir2.1 and Kir3.1 show sites for modulating gating and rectification // Nature Neuroscience. 2005. V. 8 (3). P. (In press).
7. ATP channel by ATP // J. Physiol. 1999. V. 514 (Pt 1). P. 19-25.
8. ATP channels // J. Gen. Physiol. 2002. V. 120 (3). P. 437-446.
9. ATP channel inhibition by ATP // Biophys. J. 2000. V. 79 (2). P. 841-852.
10. ATP channel inhibition by ATP // EMBO J. 1998. V. 17 (12). P. 3290-3296.
11. ATP channels. Functional coupling of Kir6.2 and SUR1 subunits // J. Gen. Physiol. 1999. V. 114 (2). P. 203-213.
12. Cukras C.A., Jeliazkova I., Nichols C.G. Structural and functional determinants of conserved lipid interaction domains of inward rectifying Kir6.2 channels // J. Gen. Physiol. 2002. V. 119 (6). P. 581-591.
13. ATP channel inhibition by ATP requires distinct functional domains of the cytoplasmic C terminus of the pore-forming subunit // Proc. Nat. Acad. Sci. USA. 1998. V. 95 (23). P. 13953-13958.
14. ATP channels // Science. 1998. V. 282 (5391). P. 1138-1141.
15. ATP channels // J. Gen. Physiol. 2000. V. 116 (5). P. 599-608.
16. ATP channel Kir6.2 subunit // EMBO J. 2005. V. 24 (2). P. 229-239.
17. ATP channel gating: toward a unified molecular understanding // Biophys. J. 2000. V. 78 (5). P. 2334-2348.
18. ATP channel // Biophys. J. 2001. V. 80 (2). P. 719-728.
19. Jiang Y., Lee A., Chen J., Cadene M., Chait B.T., MacKinnon R. Crystal structure and mechanism of a calcium-gated potassium channel // Nature. 2002. V. 417 (6888). P. 515-522.
20. + channel pore // Proc. Nat. Acad. Sci. USA. 2001. V. 98 (7). P. 4227-4232.
21. + channels in isolated guinea pig cardiac myocytes // Science. 1987. V. 238 (4823). P. 67-69.
22. ATP channel: separate roles of Kir6.2 and SUR1 subunit phosphorylation // EMBO J. 1999. V. 18 (17). P. 4722-4732.
23. Light P.E., Bladen C., Winkfein R.J., Walsh, M.P., French R.J. Molecular basis of protein kinase C-induced activation of ATP-sensitive potassium channels // Proc. Nat. Acad. Sci. USA. 2000. V. 97 (16). P. 9058-9063.
24. Branstrom R., Leibiger I.B., Leibiger B., Corkey B.E., Berggren P.-O., Larsson O. Long chain coenzyme A esters activate the pore-forming subunit (Kir6.2) of the ATP-regulated potassium channel // J. Biol. Chem. 1998. V. 273 (47). P. 31395-31400.
25. ATP channel-deficient mice // Proc. Nat. Acad. Sci. USA. 1998. V. 95 (18). P. 10402-10406.
26. ATP channel // Proc. Nat. Acad. Sci. USA. 1997. V. 94 (22). P. 11969-11973.
27. ATP channels, [see comment] // J. Clinical Invest. 2002. V. 110 (2). P. 203-208.
28. Miki T., Suzuki M., Shibasaki T., Uemura H., Sato T., Yamaguchi K., Koseki H., Iwanaga T., Nakaya H., Seino S. Mouse model of Prinzmetal angina by disruption of the inward rectifier Kir6.1 // Nat. Med. 2002. V. 8 (5). P. 466-472.
29. Yamada K., Ji J.J., Yuan H., Miki T., Sato S., Horimoto N., Shimizu T., Seino S., Inagaki N. Protective role of ATP-sensitive potassium channels in hypoxia-induced generalized seizure // Science. 2001. V. 292 (5521). P. 1543-1546.
30. Suzuki M., Li R.A., Miki T., Uemura H., Sakamoto N., Ohmoto-Sekine Y., Tamagawa M., Ogura T., Seino S., Marban E., Nakaya H. Functional roles of cardiac and vascular ATP-sensitive potassium channels clarified by Kir6.2-knockout mice // Circ. Res. 2001. V. 88 (6). P. 570-577.
31. Li R.A., Leppo M., Miki T., Seino S., Marban E. Molecular basis of electrocardiographic ST-segment elevation // Circ. Res. 2000. V. 87 (10). P. 837-839.
32. ATP channel deficiency affects resting tension, not contractile force, during fatigue in skeletal muscle [In Process Citation] // Am. J. Physiol. Cell Physiol. 2000. V. 279 (5). P. C1351-C1358.
33. Miki T., Minami K., Zhang L., Morita M., Gonoi T., Shiuchi T., Minokoshi Y., Renaud J.M., Seino S. ATP-sensitive potassium channels participate in glucose uptake in skeletal muscle and adipose tissue // Am. J. Physiol. Endocrinol. Metab. 2002. V. 283 (6). P. E1178-E1184.
34. ATP channels and insulin secretion disorders // Am. J. Physiol. Endocrinol. Metab. 2002. V. 283 (2). P. E207-E216.
35. Nestorowicz A., Nestorowicz A., Glaser B., Wilson B.A., Shyng S.L., Nichols C.G., Stanley C.A., Thornton P.S., Permutt M.A. Genetic heterogeneity in familial hyperinsulinism [published erratum appears in Hum Mol Genet 1998 Sep;7(9):1527] // Hum. Mol. Genet. 1998. V. 7 (7). P. 1119-1128.
36. ATP channel-independent regulation of insulin secretion // J. Biol. Chem. 2000. V. 275 (13). P. 9270-9277.
37. ATP channels // Proc. Nat. Acad. Sci. USA. 2002. V. 99. P. 16992-16997.
38. ATP channels // Diabetes. 2004. V. 53. P. 3159-3167.
39. ATP? // Am. J. Physiol. Endocrinol. Metab. 2002. V. 283 (3). P. E403-E412.
40. ATP channels induces profound neonatal diabetes // Cell. 2000. V. 100 (6). P. 645-654.
41. Gloyn A.L., Pearson E.R., Antcliff J.F., Proks P., Bruining G.J., Slingerland A.S., Howard N., Srinivasan S., Silva J.M., Molnes J., Edghill E.L., Frayling T.M., Temple I.K., Mackay D., Shield J.P., Sumnik Z., van Rhijn A., Wales J.K., Clark P., Gorman S. Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes // New England Journal of Medicine. 2004. V. 350. P. 1838-1849.
42. + channel subunit Kir6.2 are rare in clinically defined type 1 diabetes diagnosed before 2 years // J. Clinical Endocrinol. Metab. 2004. V. 89 (8). P. 3932-3935.
43. Massa O., Iafusco D., D'Amato E., Gloyn A.L., Hattersley A.T., Pasquino B., Tonini G., Dammacco F., Zanette G., Meschi F., Porzio O., Bottazzo G., Crino A., Lorini R., Cerutti F., Vanelli M., Barbetti F. KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes // Human Mutation. 2005. V. 25. P. 22-27.
44. Vaxillaire M., Populaire C., Busiah K., Cave H., Gloyn A.L., Hattersley A.T., Czernichow P., Froguel P., Polak M. Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients // Diabetes. 2004. V. 53. P. 2719-2722.
45. Gloyn A.L., Reimann F., Girard C., Edghill E.L., Proks P., Pearson E.R., Temple I.K., Mackay D.J., Shield J.P.H., Freedenberg D., Noyes K., Ellard S., Ashcroft F.M., Gribble P.M., Hattersley A.T. Relapsing diabetes can result from moderately activating mutations in KCNJ11 // Hum. Mol. Genet. 2005. V. 14 (7). P. 925-934.
46. Yorifuji T., Nagashima K., Kurokawa K., Kawai M.O., Akazawa Y., Hosokawa M., Yamada Y., Inagaki N., Nakahata T. The C42R mutation in the Kir6.2 (KCNJ11) gene as a cause of transient neonatal diabetes, childhood diabetes, or later-onset, apparently type 2 diabetes mellitus // J. Clinical Endocrinol. Metab. 2005. V. 90 (6). P. 3174-3178.
47. ATP channels learned from Kir6.2 genetically engineered mice // Diabetes. 2000. V. 49 (3). P. 311-318.
48. ATP connection // Diabetes. 2005. V. 54. P. 3065-3072.
49. ATP channels: function fits form // J. Gen. Physiol. 2003. V. 122. P. 471-480.
50. Kuo A., Gulbis J.M., Antcliff J.F., Rahman T., Lowe E.D., Zimmer J., Cuthbertson J., Ashcroft F.M., Ezaki T., Doyle D.A. Crystal structure of the potassium channel KirBac1.1 in the closed state // Science. 2003. V. 300 (5627). P. 1922-1926.
51. + channel Kir6.2. // J. Physiol. 2003. V. 552 (Pt. 1). P. 23-34.
52. ATP channels // J. Biol. Chem. 2000. V. 275 (2). P. 1137-1144.
53. Proks P., Kuo A., Gulbis J.M., Antcliff J.F., Rahman T., Lowe E.D., Zimmer J., Cuthbertson J., Ashcroft F.M., Ezaki T., Doyle D.A. Molecular basis of Kir6.2 mutations associated with neonatal diabetes plus neurological features // Proc. Nat. Acad. Sci. USA. 2004. V. 101. P. 17539-17544.
54. + channels in neonatal diabetes: Implications for pharmacogenomic therapy // Diabetes. 2005. V. 54. P. 2645-2654.
55. Sagen J.V., Raeder H., Hathout E., Shehadeh N., Gudmundsson K., Baevre H., Abuelo D., Phornphutkul C., Molnes J., Bell G.I., Gloyn A.L., Hattersley A.T., Molven A., Sovik O., Njolstad P.R. Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy // Diabetes. 2004. V. 53. P. 2713-2718.
56. Zung A., Glaser B., Nimri R., Zadik Z. Glibenclamide treatment in permanent neonatal diabetes mellitus due to an activating mutation in Kir6.2 // J. Clinical Endocrinol. Metab. 2004. V. 89. P. 5504-5507.
57. Sakura H., Wat N., Horton V., Millns H., Turner R.C., Ashcroft F.M. Sequence variations in the human Kir6.2 gene, a subunit of the beta-cell ATP-sensitive K-channel: no association with NIDDM in while Caucasian subjects or evidence of abnormal function when expressed in vitro // Diabetologia. 1996. V. 39 (10). P. 1233-1236.
58. + channel Kir6.2 (Bir) gene: identification and lack of role in Caucasian patients with NIDDM // Diabetes. 1997. V. 46 (3). P. 502-507.
59. + channel gene (KIR6.2/BIR): a meta-analysis suggests a role in the polyaenic basis of Type II diabetes mellitus in Caucasians // Diabetologia. 1998. V. 41 (12). P. 1511-1515.
60. Love-Gregory L., Wasson J., Lin J., Skolnick G., Suarez B., Permutt M. A. E23K single nucleotide polymorphism in the islet ATP-sensitive potassium channel gene (Kir6.2) contributes as much to the risk of Type II diabetes in Caucasians as the PPARgamma Pro 12Ala variant // Diabetologia. 2003. V. 46 (1). P. 136-137.
61. + channels // Diabetes. 2002. V. 51 (3). P. 875-879
62. Schwanstecher C., Schwanstecher M. Nucleotide sensitivity of pancreatic ATP-sensitive potassium channels and type 2 diabetes // Diabetes. 2002. V. 51. Suppl. 3. P. S358-S362.
63. Florez J.C., Burtt N., de Bakker P.I., Almgren P., Tuomi T., Holmkvist J., Gaudet D., Hudson T.J., Schaffner S.F., Daly M.J., Hirschhorn J.N., Groop L., Altshuler D. Haplotype structure and genotype-phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region // Diabetes. 2004. V. 53 (5). P. 1360-1368.
64. Nichols C.G., Lederer W.J. Adenosine triphosphate-sensitive potassium channels in the cardiovascular system // Am. J. Physiol. 1991. V. 261 (6 Pt. 2). P. H1675-H1686.
65. ATP channels in cardioprotection against ischemia/reperfusion injury in mice // J. Clin. Invest. 2002. V. 109 (4). P. 509-516.
66. ATP channels in transgenic mice // Circ. Res. 2001. V. 89 (11). P. 1022-1029.
67. ATP channels // Am. J. Physiol. Heart Circul. Physiol. 2004. V. 286 (4). P. H1361-H1369.
68. ATP channels // Am. J. Physiol. Heart Circul. Physiol. 2002. V. 283 (2). P. H584-H590
69. ATP // J. Molec. Cellular Cardiol. 2005. V. 39. P. 647-656.
70. + channel activity in intact and permeabilized rat ventricular myocytes // J. Physiol. 1990. V. 423. P. 91-110.
71. Nichols C.G., Ripoll C., Lederer W.J. ATP-sensitive potassium channel modulation of the guinea pig ventricular action potential and contraction // Circ. Res. 1991. V. 68 (1). P. 280-287.
72. + loss in hypoxic and ischaemic mammalian ventricle // J. Physiol. 1992. V. 447. P. 649-673.
73. ATP channels by SUR1 and SUR2A // J. Molec. Cellular Cardiol. 2005. V. 39. P. 491-501.