Department of Development and Stem Cells, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), 1 Rue Laurent Fries, 67404, Illkirch, France.
Centre National de la Recherche Scientifique (CNRS), Illkirch, France UMR7104.
Development. 2019 Oct 1;146(20):dev151837. doi: 10.1242/dev.151837.
Cellular senescence is a state comprising an essentially irreversible proliferative arrest combined with phenotypic changes and pronounced secretory activity. Although senescence has long been linked with aging, recent studies have uncovered functional roles for senescence in embryonic development, regeneration and reprogramming, and have helped to advance our understanding of this process as a highly coordinated and programmed cellular state. In this Primer article, we summarize some of the key findings in the field and attempt to explain them in a simple model that reconciles the normal and pathological roles for senescence. We discuss how a primary role of cellular senescence is to contribute to normal development, cell plasticity and tissue repair, as a dynamic and tightly regulated cellular program. However, when this process is perturbed, the beneficial effects turn detrimental and can contribute to disease and aging.
细胞衰老(cellular senescence)是一种包含基本不可逆的增殖停滞、表型改变和明显分泌活性的状态。尽管衰老长期以来一直与衰老有关,但最近的研究揭示了衰老在胚胎发育、再生和重编程中的功能作用,并帮助我们理解了衰老作为一种高度协调和程序化的细胞状态。在这篇基础文章中,我们总结了该领域的一些关键发现,并试图在一个简单的模型中解释它们,该模型调和了衰老的正常和病理作用。我们讨论了细胞衰老的主要作用是作为一种动态的、严格调控的细胞程序,为正常发育、细胞可塑性和组织修复做出贡献。然而,当这个过程受到干扰时,有益的效果就会变成有害的,并导致疾病和衰老。