Louch William E, Koivumäki Jussi T, Tavi Pasi
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.
J Physiol. 2015 Mar 1;593(5):1047-63. doi: 10.1113/jphysiol.2014.274712. Epub 2015 Feb 9.
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.
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。