Cellular senescence and the skeleton: pathophysiology and therapeutic implications

被引:52
|
作者
Khosla, Sundeep
Farr, Joshua N.
Monroe, David G.
机构
[1] Mayo Clin, Kogod Ctr Aging, Rochester, MN 55905 USA
[2] Mayo Clin, Div Endocrinol & Metab, Rochester, MN 55905 USA
来源
JOURNAL OF CLINICAL INVESTIGATION | 2022年 / 132卷 / 03期
关键词
DEFICIENCY-INDUCED OSTEOPOROSIS; INHIBITING OXIDATIVE STRESS; SECRETORY PHENOTYPE; OSTEOBLAST DIFFERENTIATION; DIABETES-MELLITUS; BONE LOSS; CELLS; DNA; AGE; DETERMINANTS;
D O I
10.1172/JCI154888
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cellular senescence is a fundamental aging mechanism that is currently the focus of considerable interest as a pathway that could be targeted to ameliorate aging across multiple tissues, including the skeleton. There is now substantial evidence that senescent cells accumulate in the bone microenvironment with aging and that targeting these cells prevents age-related bone loss, at least in mice. Cellular senescence also plays important roles in mediating the skeletal fragility associated with diabetes mellitus, radiation, and chemotherapy. As such, there are ongoing efforts to develop "senolytic" drugs that kill senescent cells by targeting key survival mechanisms in these cells without affecting normal cells. Because senescent cells accumulate across tissues with aging, senolytics offer the attractive possibility of treating multiple age-related comorbidities simultaneously.
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页数:10
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