Brief Funct Genomics. 2022 Jan 25;21(1):24-34. doi: 10.1093/bfgp/elab012.
Cellular senescence is the irreversible cell cycle arrest in response to DNA damage. Because senescent cells accumulate with age and contribute to chronic inflammation, they are promising therapeutic targets for healthspan extension. The senescent phenotype can vary depending on cell type and on the specific insults that induce senescence. This variability is also reflected in the extensive remodeling of the genome organization within the nucleus of senescent cells. Here, we give an overview of the nuclear changes that occur in different forms of senescence, including changes to chromatin state and composition and to the three-dimensional organization of the genome, as well as alterations to the nuclear envelope and to the accessibility of repetitive genomic regions. Many of these changes are shared across all forms of senescence, implicating nuclear organization as a fundamental driver of the senescent state and of how senescent cells interact with the surrounding tissue.
细胞衰老(cellular senescence)是细胞对 DNA 损伤做出的不可逆性细胞周期停滞反应。由于衰老细胞会随着年龄的增长而积累,并导致慢性炎症,因此它们是延长健康寿命的有前途的治疗靶点。衰老表型可能因细胞类型和诱导衰老的特定损伤而异。这种可变性也反映在衰老细胞核内基因组组织的广泛重塑中。在这里,我们概述了不同形式的衰老中发生的核变化,包括染色质状态和组成的变化,以及基因组三维结构的变化,以及核膜的改变和重复基因组区域的可及性的改变。这些变化中有许多是所有形式的衰老所共有的,这表明核组织是衰老状态的一个基本驱动因素,也是衰老细胞如何与周围组织相互作用的一个基本驱动因素。