Literature DB >> 9159640

Inwardly rectifying potassium channels: their molecular heterogeneity and function.

S Isomoto1, C Kondo, Y Kurachi.   

Abstract

A variety of cells including cardiac myocytes and neuronal cells possess inwardly rectifying K+ (Kir) channels through which currents flow more readily in the inward direction than outward. These K+ channels play pivotal roles in maintenance of the resting membrane potential, in regulation of the action potential duration, in receptor-dependent inhibition of cellular excitability, and in the secretion and absorption of K+ ions across cell membrane. Recent molecular biological dissection has shown that the DNAs encoding Kir channels constitute a new family of K+ channels whose subunits contain two putative transmembrane domains and a pore-forming region. So far, more than ten cDNAs of Kir channel subunits have been isolated and classified into four subfamilies: 1) IRK subfamily (IRK1-3/Kir1.1-1.3), 2) GIRK subfamily (GIRK1-4/Kir3.1-3.4), 3) ATP-dependent Kir subfamily (ROMK1/Kir1.1, K(AB)-2/Kir4.1), and 4) ATP-sensitive Kir subfamily (uKATP-1/Kir6.1, BIR/Kir6.2). Xenopus oocytes injected with the cRNAs of IRKs elicit classical Kir channel currents. GIRKs, as heteromultimers, compose the G protein-gated Kir (KG) channels, which are regulated by a variety of Gi/Go-coupled inhibitory neurotransmitter receptors such as m2-mus-carinic, serotonergic (5HT1A), GABAB, somatostatin and opioid (mu, delta, kappa) receptors. ROMK1 and KAB-2 are characterized with a Walker type-A ATP-binding motif in their carboxyl termini, and may be involved in K+ transport in renal epithelial and brain glial cells. uKATP-1 and BIR form with sulfonylurea receptors, the so-called ATP-sensitive K+ channels. Thus, it is a feature of the Kir channel family that each subfamily plays a specific physiological functional role. The (Na+)-activated Kir channels identified electrophysiologically in neurons and cardiac myocytes have not yet been cloned. In this review, we overviewed the current understandings of the features of the molecular structures and functions of the four main subfamilies of Kir channels.

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Year:  1997        PMID: 9159640     DOI: 10.2170/jjphysiol.47.11

Source DB:  PubMed          Journal:  Jpn J Physiol        ISSN: 0021-521X


  59 in total

1.  Expression and polarized distribution of an inwardly rectifying K+ channel, Kir4.1, in rat retinal pigment epithelium.

Authors:  S Kusaka; Y Horio; A Fujita; K Matsushita; A Inanobe; T Gotow; Y Uchiyama; Y Tano; Y Kurachi
Journal:  J Physiol       Date:  1999-10-15       Impact factor: 5.182

2.  Supralinear summation of synaptic inputs by an invertebrate neuron: dendritic gain is mediated by an "inward rectifier" K(+) current.

Authors:  R Wessel; W B Kristan; D Kleinfeld
Journal:  J Neurosci       Date:  1999-07-15       Impact factor: 6.167

3.  Regulation of ATP-sensitive potassium channel function by protein kinase A-mediated phosphorylation in transfected HEK293 cells.

Authors:  Y F Lin; Y N Jan; L Y Jan
Journal:  EMBO J       Date:  2000-03-01       Impact factor: 11.598

4.  Increased inwardly rectifying potassium currents in HEK-293 cells expressing murine transient receptor potential 4.

Authors:  Z Zhang; Y Tang; M X Zhu
Journal:  Biochem J       Date:  2001-03-15       Impact factor: 3.857

5.  G protein-activated inwardly rectifying K+ (GIRK) currents in dendrites of rat neocortical pyramidal cells.

Authors:  T Takigawa; C Alzheimer
Journal:  J Physiol       Date:  1999-06-01       Impact factor: 5.182

6.  Regulation of inwardly rectifying K+ channels in retinal pigment epithelial cells by intracellular pH.

Authors:  Yukun Yuan; Masahiko Shimura; Bret A Hughes
Journal:  J Physiol       Date:  2003-03-28       Impact factor: 5.182

Review 7.  Molecular substrates of potassium spatial buffering in glial cells.

Authors:  Paulo Kofuji; Nathan C Connors
Journal:  Mol Neurobiol       Date:  2003-10       Impact factor: 5.590

8.  Background and tandem-pore potassium channels in magnocellular neurosecretory cells of the rat supraoptic nucleus.

Authors:  Jaehee Han; Carmen Gnatenco; Celia D Sladek; Donghee Kim
Journal:  J Physiol       Date:  2003-02-01       Impact factor: 5.182

9.  Characterization of four types of background potassium channels in rat cerebellar granule neurons.

Authors:  Jaehee Han; Jeffrey Truell; Carmen Gnatenco; Donghee Kim
Journal:  J Physiol       Date:  2002-07-15       Impact factor: 5.182

10.  Influence of inhibitory serotonergic inputs to orexin/hypocretin neurons on the diurnal rhythm of sleep and wakefulness.

Authors:  Sawako Tabuchi; Tomomi Tsunematsu; Thomas S Kilduff; Shouta Sugio; Ming Xu; Kenji F Tanaka; Satoru Takahashi; Makoto Tominaga; Akihiro Yamanaka
Journal:  Sleep       Date:  2013-09-01       Impact factor: 5.849

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