连接蛋白
缝隙连接
心力衰竭
心源性猝死
基因亚型
线粒体
细胞生物学
肥厚性心肌病
缺血
生物
心功能曲线
心肌病
内科学
细胞内
神经科学
医学
生物化学
基因
作者
Michela Pecoraro,Verrilli Velia,Aldo Pinto,Ada Popolo
标识
DOI:10.1016/j.ejphar.2015.10.030
摘要
Gap junctions (GJs) channels provide the basis for intercellular communication in the cardiovascular system for maintenance of the normal cardiac rhythm, regulation of vascular tone and endothelial function as well as metabolic interchange between the cells. They allow the transfer of small molecules and may enable slow calcium wave spreading, transfer of "death" or of "survival" signals. In the cardiomyocytes the most abundant isoform is Connexin 43 (Cx43). Alterations in Cx43 expression and distribution were observed in myocardium disease; i.e. in hypertrophic cardiomyopathy, heart failure and ischemia. Recent reports suggest the presence of Cx43 in the mitochondria as well, at least in the inner mitochondrial membrane, where it plays a central role in ischemic preconditioning. In this review, the current knowledge on the relationship between the remodeling of cardiac gap junctions and cardiac diseases are summarized.
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