作者
Binsheng Wang,Lichao Wang,Nathan S. 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,Tamar Tchkonia,Sumit Yadav,Laura Haynes,James L. Kirkland,Yuji Ikeno,Ming Xu
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.