Medical Scientist Training Program, University of Pittsburgh and Carnegie Mellon University, Pittsburgh, PA 15219, USA.
Division of Cardiology, UPMC Children's Hospital of Pittsburgh and Department of Pediatrics, 4401 Penn Ave, Pittsburgh, PA 15224, USA.
Development. 2021 Jul 15;148(14). doi: 10.1242/dev.199401. Epub 2021 Jul 26.
Terminally differentiated cells are generally thought to have arrived at their final form and function. Many terminally differentiated cell types are polyploid, i.e. they have multiple copies of the normally diploid genome. Mammalian heart muscle cells, termed cardiomyocytes, are one such example of polyploid cells. Terminally differentiated cardiomyocytes are bi- or multi-nucleated, or have polyploid nuclei. Recent mechanistic studies of polyploid cardiomyocytes indicate that they can limit cellular proliferation and, hence, heart regeneration. In this short Spotlight, we present the mechanisms generating bi- and multi-nucleated cardiomyocytes, and the mechanisms generating polyploid nuclei. Our aim is to develop hypotheses about how these mechanisms might relate to cardiomyocyte proliferation and cardiac regeneration. We also discuss how these new findings could be applied to advance cardiac regeneration research, and how they relate to studies of other polyploid cells, such as cancer cells.
终末分化细胞通常被认为已经达到其最终的形态和功能。许多终末分化的细胞类型是多倍体的,即它们具有正常二倍体基因组的多个拷贝。哺乳动物心肌细胞,称为心肌细胞,就是多倍体细胞的一个例子。终末分化的心肌细胞是二倍体或多倍体的,或者具有多倍体核。最近对多倍体心肌细胞的机制研究表明,它们可以限制细胞增殖,从而限制心脏再生。在这个简短的焦点介绍中,我们介绍了产生双核和多核心肌细胞的机制,以及产生多倍体核的机制。我们的目的是提出关于这些机制如何与心肌细胞增殖和心脏再生相关的假设。我们还讨论了这些新发现如何应用于推进心脏再生研究,以及它们与其他多倍体细胞(如癌细胞)研究的关系。