Literature DB >> 26043299

PKC and AMPK regulation of Kv1.5 potassium channels.

Martin Nybo Andersen1, Lasse Skibsbye, Chuyi Tang, Frederic Petersen, Nanna MacAulay, Hanne Borger Rasmussen, Thomas Jespersen.   

Abstract

The voltage-gated Kv1.5 potassium channel, conducting the ultra-rapid rectifier K(+) current (IKur), is regulated through several pathways. Here we investigate if Kv1.5 surface expression is controlled by the 2 kinases PKC and AMPK, using Xenopus oocytes, MDCK cells and atrial derived HL-1 cells. By confocal microscopy combined with electrophysiology we demonstrate that PKC activation reduces Kv1.5 current, through a decrease in membrane expressed channels. AMPK activation was found to decrease the membrane expression in MDCK cells, but not in HL-1 cells and was furthermore shown to be dependent on co-expression of Nedd4-2 in Xenopus oocytes. These results indicate that Kv1.5 channels are regulated by both kinases, although through different molecular mechanisms in different cell systems.

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Year:  2015        PMID: 26043299      PMCID: PMC4594233          DOI: 10.1080/19336950.2015.1036205

Source DB:  PubMed          Journal:  Channels (Austin)        ISSN: 1933-6950            Impact factor:   2.581


  34 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-17       Impact factor: 11.205

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7.  AMP-activated protein kinase inhibits Kv 1.5 channel currents of pulmonary arterial myocytes in response to hypoxia and inhibition of mitochondrial oxidative phosphorylation.

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