Department of Medicine, Università degli Studi di Udine. P.le Kolbe 4, 33100 Udine, Italy.
Cells. 2020 Feb 18;9(2):466. doi: 10.3390/cells9020466.
Senescence is the end point of a complex cellular response that proceeds through a set of highly regulated steps. Initially, the permanent cell-cycle arrest that characterizes senescence is a pro-survival response to irreparable DNA damage. The maintenance of this prolonged condition requires the adaptation of the cells to an unfavorable, demanding and stressful microenvironment. This adaptation is orchestrated through a deep epigenetic resetting. A first wave of epigenetic changes builds a dam on irreparable DNA damage and sustains the pro-survival response and the cell-cycle arrest. Later on, a second wave of epigenetic modifications allows the genomic reorganization to sustain the transcription of pro-inflammatory genes. The balanced epigenetic dynamism of senescent cells influences physiological processes, such as differentiation, embryogenesis and aging, while its alteration leads to cancer, neurodegeneration and premature aging. Here we provide an overview of the most relevant histone modifications, which characterize senescence, aging and the activation of a prolonged DNA damage response.
衰老(senescence)是细胞经历一系列高度调控的步骤而达到的终点状态。最初,永久性细胞周期阻滞是衰老的特征,它是对不可修复的 DNA 损伤的一种存活保护反应。维持这种长期状态需要细胞适应不利的、苛刻的和应激的微环境。这种适应是通过深刻的表观遗传重置(epigenetic resetting)来协调的。第一波表观遗传改变在不可修复的 DNA 损伤上建立了一道堤坝,维持着存活保护反应和细胞周期阻滞。后来,第二波表观遗传修饰允许基因组重排,以维持促炎基因的转录。衰老细胞的平衡的表观遗传动态影响着分化、胚胎发生和衰老等生理过程,而其改变则导致癌症、神经退行性变和早衰。在这里,我们提供了一个概述,介绍了与衰老、老化和长期 DNA 损伤反应激活相关的最相关的组蛋白修饰。