| Literature DB >> 34897388 |
Anna Kirillova1, Lu Han2,3, Honghai Liu2,3, Bernhard Kühn2,3,4.
Abstract
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.Entities:
Keywords: Cardiomyocytes; Cytokinesis; Differentiation; Karyokinesis; Ploidy; Regeneration
Mesh:
Year: 2021 PMID: 34897388 PMCID: PMC8326922 DOI: 10.1242/dev.199401
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.862