神经发生
DNA去甲基化
生物
神经干细胞
海马结构
抗抑郁药
海马体
DNA甲基化
去甲基化
细胞生物学
内分泌学
干细胞
遗传学
基因表达
基因
作者
Le Zhang,Qingfeng Li,Huan Wang,Yuanfei Wu,Xiujuan Ye,Zhuo Gong,Qingqing Li,Aiguo Xuan
出处
期刊:Stem Cells
[Oxford University Press]
日期:2022-01-01
卷期号:40 (1): 59-73
被引量:16
标识
DOI:10.1093/stmcls/sxab001
摘要
Increased neurogenesis elicits antidepressive-like effects. The antidiabetic drug metformin (Met) reportedly promotes hippocampal neurogenesis, which ameliorates spatial memory deficits and depression-like behaviors. However, the precise molecular mechanisms underpinning Met-induced neuronal differentiation of neural stem cells (NSCs) remain unclear. We showed that Met enhanced neuronal differentiation of NSCs via Gadd45g but not Gadd45a and Gadd45b. We further found that Gadd45g increased demethylation of neurogenic differentiation 1 promoter by regulating the activity of passive and active DNA demethylation enzymes through an adenylate-activated protein kinase -independent mechanism in Met-treated NSCs. Importantly, genetic deficiency of Gadd45g decreased hippocampal neurogenesis, which could contribute to spatial memory decline, and depression-like behaviors in the adult mice, whereas forced expression of Gadd45g alleviated the depressive-like behaviors. Our findings provide a model that Gadd45g-mediated DNA demethylation contributes to Met-induced neuronal genesis and its antidepressant-like effects and propose the concept that targeting Gadd45g regulation of neurogenesis might serve as a novel antidepressant strategy.
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