刺
内部收益率3
衰老
干扰素基因刺激剂
细胞生物学
DNA损伤
干扰素调节因子
ULK1
干扰素
信号转导
彪马
癌症研究
生物
先天免疫系统
激酶
免疫学
蛋白激酶A
免疫系统
遗传学
细胞凋亡
DNA
工程类
安普克
航空航天工程
作者
Qirou Wu,Xiaohong Leng,Qian Zhang,Yezhang Zhu,Ruyuan Zhou,Yutong Liu,Mei Chen,Dan Zhang,Shengduo Liu,S. Chen,Xiaojian Wang,Aifu Lin,Xia Lin,Tingbo Liang,Li Shen,Xin‐Hua Feng,Bing Xia,Pinglong Xu
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2024-03-01
卷期号:10 (9)
被引量:3
标识
DOI:10.1126/sciadv.adj2102
摘要
Cytosolic double-stranded DNA surveillance by cyclic GMP-AMP synthase (cGAS)-Stimulator of Interferon Genes (STING) signaling triggers cellular senescence, autophagy, biased mRNA translation, and interferon-mediated immune responses. However, detailed mechanisms and physiological relevance of STING-induced senescence are not fully understood. Here, we unexpectedly found that interferon regulatory factor 3 (IRF3), activated during innate DNA sensing, forms substantial endogenous complexes in the nucleus with retinoblastoma (RB), a key cell cycle regulator. The IRF3-RB interaction attenuates cyclin-dependent kinase 4/6 (CDK4/6)-mediated RB hyperphosphorylation that mobilizes RB to deactivate E2 family (E2F) transcription factors, thereby driving cells into senescence. STING-IRF3-RB signaling plays a notable role in hepatic stellate cells (HSCs) within various murine models, pushing activated HSCs toward senescence. Accordingly, IRF3 global knockout or conditional deletion in HSCs aggravated liver fibrosis, a process mitigated by the CDK4/6 inhibitor. These findings underscore a straightforward yet vital mechanism of cGAS-STING signaling in inducing cellular senescence and unveil its unexpected biology in limiting liver fibrosis.
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