Mechanisms of enhanced quiescence in neural stem cell aging

被引:34
作者
Audesse, Amanda J. [1 ,2 ]
Webb, Ashley E. [2 ,3 ,4 ]
机构
[1] Brown Univ, Grad Program Neurosci, Providence, RI 02912 USA
[2] Brown Univ, Dept Mol Biol Cell Biol & Biochem, Providence, RI 02912 USA
[3] Brown Univ, Carney Inst Brain Sci, Providence, RI 02912 USA
[4] Brown Univ, Ctr Biol Aging, Providence, RI 02912 USA
关键词
Adult neurogenesis; Aging; Cognitive decline; Neural stem cell; NSC; Quiescence; AGE-RELATED DECREASE; HIPPOCAMPAL NEUROGENESIS; SUBVENTRICULAR ZONE; PROGENITOR CELLS; SELF-RENEWAL; DENTATE GYRUS; ADULT NEUROGENESIS; COGNITIVE FUNCTION; DNA DEMETHYLATION; OLFACTORY-BULB;
D O I
10.1016/j.mad.2020.111323
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The maintenance of neural stem cell function is vital to ensure neurogenesis throughout adulthood. During aging, there is a significant reduction in adult neurogenesis that correlates with a decline in cognitive function. Although recent studies have revealed novel extrinsic and intrinsic mechanisms that regulate the adult neural stem cell (NSC) pool and lineage progression, the precise molecular mechanisms that drive dysregulation of adult neurogenesis in the context of aging are only beginning to emerge. Recent studies have shed light on mechanisms that regulate the earliest step of adult neurogenesis, the activation of quiescent NSCs. Interestingly, the ability of NSCs to enter the cell cycle in the aged brain significantly declines suggesting a deepend state of quiescence. Given the likely contribution of adult neurogenesis to supporting cognitive function in humans, enhancing neurogenesis may be a strategy to combat age-related cognitive decline. This review highlights the mechanisms that regulate the NSC pool throughout adulthood and discusses how dysregulation of these processes may contribute to the decline in neurogenesis and cognitive function throughout aging.
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页数:7
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