Altered expression of genes for Kir ion channels in dilated cardiomyopathy.

Abstract:

:Dilated cardiomyopathy (DCM) is a multifactorial disease characterized by left ventricular dilation that is associated with systolic dysfunction and increased action potential duration. The Kir2.x K⁺ channels (encoded by KCNJ genes) regulate the inward rectifier current (IK1) contributing to the final repolarization in cardiac muscle. Here, we describe the transitions in the gene expression profiles of 4 KCNJ genes from healthy or dilated cardiomyopathic human hearts. In the healthy adult ventricles, KCNJ2, KCNJ12, and KCNJ4 (Kir2.1-2.3, respectively) genes were expressed at high levels, while expression of the KCNJ14 (Kir2.4) gene was low. In DCM ventricles, the levels of Kir2.1 and Kir2.3 were upregulated, but those of Kir2.2 channels were downregulated. Additionally, the expression of the DLG1 gene coding for the synapse-associated protein 97 (SAP97) anchoring molecule exhibited a 2-fold decline with increasing age in normal hearts, and it was robustly downregulated in young DCM patients. These adaptations could offer a new aspect for the explanation of the generally observed physiological and molecular alterations found in DCM.

authors

Szuts V,Ménesi D,Varga-Orvos Z,Zvara Á,Houshmand N,Bitay M,Bogáts G,Virág L,Baczkó I,Szalontai B,Geramipoor A,Cotella D,Wettwer E,Ravens U,Deák F,Puskás LG,Papp JG,Kiss I,Varró A,Jost N

doi

10.1139/cjpp-2012-0413

subject

Has Abstract

pub_date

2013-08-01 00:00:00

pages

648-56

issue

8

eissn

0008-4212

issn

1205-7541

journal_volume

91

pub_type

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