Stem cell rejuvenation and the role of autophagy in age retardation by caloric restriction: An update

被引:16
作者
Bi, Shanrong [1 ]
Wang, Hanyu [1 ]
Kuang, Weihong [1 ]
机构
[1] Guangzhou Univ Chinese Med, Affiliated Hosp 1, 12 Jichang Rd, Guangzhou 510405, Guangdong, Peoples R China
关键词
Autophagy; Caloric restriction; Stem cell aging; Age retardation; ROS; ACTIVATED PROTEIN-KINASE; OXYGEN SPECIES PRODUCTION; FOXO TRANSCRIPTION FACTORS; DIETARY RESTRICTION; LIFE-SPAN; DNA-DAMAGE; MITOCHONDRIAL DYSFUNCTION; AGING PROCESS; PROTON LEAK; MUSCLE;
D O I
10.1016/j.mad.2018.07.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Stem cells being pluripotent in nature can differentiate into a wide array of specific cells and asymmetrically divide to produce new ones but may undergo aging by themselves. Aging has both quantitative and qualitative effects on stem cells, and could eventually restrain them from replenishing into progenitor cells. Reactive oxygen species (ROS) accumulated in the aging cells could not only block the cell cycle but also affect autophagy by damaging the mitochondria. Autophagy could eliminate redundant production of ROS in aging stem cells and helps to maintain the proliferation capacity by restraining the expression of p16(INK4a). Current studies showed that improving autophagy could restore the regenerative ability of aging stem cells. Therefore, it is important for an organism to maintain the appropriate autophagy. Caloric restriction (CR) was shown to retard the stem cell aging by a certain basic level of autophagy, suggesting that CR was an effective way to extend longevity in mammals. However, little is known about the underlying mechanisms. In this review, we tried to explore the molecular mechanisms on how CR induces appropriate autophagy to restore aging stem cell regenerative ability.
引用
收藏
页码:46 / 54
页数:9
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