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发育中心肌细胞的钙信号传导:对模型系统和疾病的影响

Calcium signalling in developing cardiomyocytes: implications for model systems and disease.

作者信息

Louch William E, Koivumäki Jussi T, Tavi Pasi

机构信息

Institute for Experimental Medical Research, Oslo University Hospital and University of Oslo, 0424, Oslo, Norway; K. G. Jebsen Cardiac Research Center and Center for Heart Failure Research, University of Oslo, 0316, Oslo, Norway.

出版信息

J Physiol. 2015 Mar 1;593(5):1047-63. doi: 10.1113/jphysiol.2014.274712. Epub 2015 Feb 9.

Abstract

Adult cardiomyocytes exhibit complex Ca(2+) homeostasis, enabling tight control of contraction and relaxation. This intricate regulatory system develops gradually, with progressive maturation of specialized structures and increasing capacity of Ca(2+) sources and sinks. In this review, we outline current understanding of these developmental processes, and draw parallels to pathophysiological conditions where cardiomyocytes exhibit a striking regression to an immature state of Ca(2+) homeostasis. We further highlight the importance of understanding developmental physiology when employing immature cardiomyocyte models such as cultured neonatal cells and stem cells.

摘要

成年心肌细胞表现出复杂的钙(Ca2+)稳态,从而实现对收缩和舒张的严格控制。这种复杂的调节系统是逐渐发展起来的,伴随着特殊结构的逐步成熟以及钙(Ca2+)来源和汇的能力不断增强。在这篇综述中,我们概述了目前对这些发育过程的理解,并将其与病理生理状况进行对比,在这些病理生理状况下,心肌细胞表现出向钙(Ca2+)稳态不成熟状态的显著退化。我们还强调了在使用未成熟心肌细胞模型(如培养的新生细胞和干细胞)时理解发育生理学的重要性。

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