Maximizing Longevity and Healthspan: Multiple Approaches All Converging on Autophagy

被引:32
作者
Bareja, Akshay [1 ]
Lee, David E. [1 ]
White, James P. [1 ,2 ,3 ]
机构
[1] Duke Univ, Sch Med, Duke Mol Physiol Inst, Durham, NC 27708 USA
[2] Duke Univ, Sch Med, Dept Med, Div Hematol, Durham, NC 27706 USA
[3] Duke Univ, Sch Med, Duke Ctr Study Aging & Human Dev, Durham, NC 27708 USA
关键词
autophagy; longevity; aging; exercise; healthspan; ACTIVATED PROTEIN-KINASE; EXTENDS LIFE-SPAN; SKELETAL-MUSCLE; INSULIN-RESISTANCE; CALORIE RESTRICTION; EXERCISE; AMPK; HOMOCYSTEINE; RECEPTOR; SIRT1;
D O I
10.3389/fcell.2019.00183
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Our understanding of the molecular basis of aging has greatly increased over the past few decades. In this review, we provide an overview of the key signaling pathways associated with aging, and whose modulation has been shown to extend lifespan in a range of model organisms. We also describe how these pathways converge onto autophagy, a catabolic process that functions to recycle dysfunctional cellular material and maintains energy homeostasis. Finally, we consider various approaches of therapeutically modulating these longevity pathways, highlighting exercise as a potent geroprotector.
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页数:8
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