炎症
促炎细胞因子
功能(生物学)
转录组
寿命延长
细胞生物学
老年学
长寿
生物
癌症研究
生理学
医学
免疫学
遗传学
基因
基因表达
作者
Binsheng Wang,Lichao Wang,Nathan Gasek,Chia‐Ling Kuo,Jia Nie,Taewan Kim,Pengyi Yan,Junyu Zhu,Blake L. Torrance,Yueying Zhou,Lisa C. Flores,Colton Allen,Allison M. Andrade,Chun Guo,Rachel Cohn,Evan R. Jellison,Jenna M. Bartley,George A. Kuchel,Sheng Li,Tamar Pirtskhalava
出处
期刊:Cell Metabolism
[Cell Press]
日期:2024-08-01
卷期号:36 (8): 1795-1805.e6
被引量:9
标识
DOI:10.1016/j.cmet.2024.07.006
摘要
A key challenge in aging research is extending lifespan in tandem with slowing down functional decline so that life with good health (healthspan) can be extended. Here, we show that monthly clearance, starting from 20 months, of a small number of cells that highly express p21Cip1 (p21high) improves cardiac and metabolic function and extends both median and maximum lifespans in mice. Importantly, by assessing the health and physical function of these mice monthly until death, we show that clearance of p21high cells improves physical function at all remaining stages of life, suggesting healthspan extension. Mechanistically, p21high cells encompass several cell types with a relatively conserved proinflammatory signature. Clearance of p21high cells reduces inflammation and alleviates age-related transcriptomic signatures of various tissues. These findings demonstrate the feasibility of healthspan extension in mice and indicate p21high cells as a therapeutic target for healthy aging.
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