衰老
自噬
关贸总协定
转录因子
DNA损伤
细胞生物学
炎症
生物
抑制器
表型
癌症研究
免疫学
DNA
遗传学
细胞凋亡
基因
作者
Chanhee Kang,Qikai Xu,Timothy D. Martin,Mamie Z. Li,Marco Demaria,Liviu Aron,Tao Lu,Bruce A. Yankner,Judith Campisi,Stephen J. Elledge
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2015-09-24
卷期号:349 (6255): aaa5612-aaa5612
被引量:938
标识
DOI:10.1126/science.aaa5612
摘要
Transcriptional control of cell senescence Senescent cells that have stopped proliferating secrete molecules that influence the cells around them. Prevention of this senescence-activated secretory phenotype seems to slow organismal aging. Kang et al. explored the regulatory process behind cell senescence and found that DNA damage led to stabilization of the transcription factor GATA4 (see the Perspective by Cassidy and Narita). Increased activity of GATA4 in senescent cells stimulated genes encoding secreted factors. GATA4 also accumulates in the brains of aging mice or humans. Science , this issue 10.1126/science.aaa5612 ; see also p. 1448
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