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Alterations in cardiac connexin expression in cardiomyopathies.

Severs, NJ, Dupont, E, Thomas, N, Kaba, R, Rothery, S, Jain, R, Sharpey, K and Fry, CH (2006) Alterations in cardiac connexin expression in cardiomyopathies. Adv Cardiol, 42. pp. 228-242.

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Gap junctions, assembled from connexins, form the cell-to-cell pathways for propagation of the precisely orchestrated patterns of current flow that govern the synchronized rhythm of the healthy heart. As in most tissues and organs, multiple connexin types are co-expressed in the heart; the connexins Cx43, Cx40 and Cx45 are found in distinctive combinations and relative quantities in different, functionally specialized subsets of cardiomyocytes. Alterations in connexin expression and gap junction organization, now a well-documented feature of human cardiomyopathies, potentially contribute to the pro-arrhythmic substrate. In the diseased ventricle, the most consistently reported quantitative alteration involves heterogeneous reduction in Cx43 expression and disruption of the normal ordered pattern of Cx43 gap junction distribution. Additional studies suggest that upregulation of Cx40 and Cx45 may also feature in the failing ventricle, the former restricted to ischemic cardiomyopathy and localized to the subendocardial region. By correlating data from studies on the human patient with those from animal and cell models, alterations in connexin expression and gap junction organization have emerged as important factors to be considered in understanding the pro-arrhythmic substrate found in human cardiomyopathies.

Item Type: Article
Authors :
Severs, NJ
Dupont, E
Thomas, N
Kaba, R
Rothery, S
Jain, R
Sharpey, K
Fry, CH
Date : 2006
DOI : 10.1159/000092572
Uncontrolled Keywords : Animals, Blotting, Western, Cardiomyopathies, Connexin 43, Connexins, Gap Junctions, Heart Ventricles, Humans, Myocardium, Myocytes, Cardiac, Up-Regulation, Ventricular Remodeling
Depositing User : Symplectic Elements
Date Deposited : 28 Mar 2017 15:50
Last Modified : 31 Oct 2017 14:25

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