衰老
DNA损伤
生物
下调和上调
细胞生物学
趋化因子受体
趋化因子
癌症研究
受体
基因
DNA
遗传学
作者
Haiyang Guo,Zhaojian Liu,Bing Xu,Huili Hu,Wei Zhao,Qiao Li,Xiyu Zhang,Xuebin Ding,Yu Wang,Minnan Zhao,Yaoqin Gong,Changshun Shao
出处
期刊:Aging Cell
[Wiley]
日期:2013-09-08
卷期号:12 (6): 1110-1121
被引量:44
摘要
Summary Mammalian cells may undergo permanent growth arrest/senescence when they incur excessive DNA damage. As a key player during DNA damage response ( DDR ), p53 transactivates an array of target genes that are involved in various cellular processes including the induction of cellular senescence. Chemokine receptor CXCR 2 was previously reported to mediate replicative and oncogene‐induced senescence in a DDR and p53‐dependent manner. Here, we report that CXCR 2 is upregulated in various types of cells in response to genotoxic or oxidative stress. Unexpectedly, we found that the upregulation of CXCR 2 depends on the function of p53. Like other p53 target genes such as p21, CXCR 2 is transactivated by p53. We identified a p53‐binding site in the CXCR 2 promoter that responds to changes in p53 functional status. Thus, CXCR 2 may act downstream of p53. While the senescence‐associated secretory phenotype (SASP) exhibits a kinetics that is distinct from that of CXCR 2 expression and does not require p53, it reinforces senescence. We further showed that the cellular senescence caused by CXCR 2 upregulation is mediated by p38 activation. Our results thus demonstrate CXCR 2 as a critical mediator of cellular senescence downstream of p53 in response to DNA damage.
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