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Gadd45g,一种新型抗抑郁靶点,通过 DNA 去甲基化介导二甲双胍诱导的神经干细胞神经元分化。

Gadd45g, A Novel Antidepressant Target, Mediates Metformin-Induced Neuronal Differentiation of Neural Stem Cells Via DNA Demethylation.

机构信息

Institute of Neuroscience and the Second Affiliated Hospital of Guangzhou Medical University, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou 510260, People's Republic of China.

Key Laboratory of Neurological Function and Health, School of Basic Medical Sciences, Guangzhou Medical University, Guangzhou 511436, People's Republic of China.

出版信息

Stem Cells. 2022 Mar 3;40(1):59-73. doi: 10.1093/stmcls/sxab001.

Abstract

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.

摘要

神经发生增加会产生抗抑郁样作用。据报道,抗糖尿病药物二甲双胍(Met)可促进海马神经发生,从而改善空间记忆缺陷和抑郁样行为。然而,Met 诱导神经干细胞(NSC)神经元分化的确切分子机制尚不清楚。我们发现 Met 通过 Gadd45g 而非 Gadd45a 和 Gadd45b 增强 NSC 的神经元分化。我们进一步发现,Gadd45g 通过调节被动和主动 DNA 去甲基化酶的活性,通过腺嘌呤激活蛋白激酶非依赖性机制,增加神经发生分化 1 启动子的去甲基化,从而增加 Met 处理后的 NSC 中的神经元分化。重要的是,Gadd45g 的遗传缺陷减少了海马神经发生,这可能导致成年小鼠空间记忆下降和抑郁样行为,而 Gadd45g 的强制表达则缓解了抑郁样行为。我们的研究结果提供了一个模型,即 Gadd45g 介导的 DNA 去甲基化有助于 Met 诱导的神经元发生及其抗抑郁样作用,并提出了靶向 Gadd45g 调节神经发生可能作为一种新的抗抑郁策略的概念。

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