The Mechanisms of Melatonin’s Regulatory Functions on Neural Stem Cells’ Survival, Proliferation and Differentiation

Asuku Abraham Olufemi, A. M. Tayo, Ajibare Ayodeji Johnson, Adeyemo Michael Bolaji, Adeyemo Racheal Oluremi, Olajide Tobiloba Samuel
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Abstract

Neural stem cells (NSCs) are cells that can self-replicate and differentiate in the central nervous system into neurons and glial cells. The sub granular zone (SGZ) in the hippocampal dentate gyrus (DG) and the sub ventricular zone (SVZ) are the two principal locations where NSCs are discovered in the adult brain. The recent identification of NSCs in adult mammalian brains has sparked a flurry of preclinical and translational research to examine brand-new strategies for treating neurodegenerative illnesses. Therefore, mobilizing endogenous NSCs has become a possible therapeutic strategy for brain repair. The main secretory substance produced and released by the pineal gland is melatonin, which has a wide range of biological functions. Melatonin has recently been shown to play a significant role in NSCs, including their proliferation, differentiation, and survival. These processes are regulated by a variety of factors such as the MAPK/ERK signaling pathway, histone acetylation, neurotrophic factors, and apoptotic genes that are discussed in this review.
褪黑素对神经干细胞存活、增殖和分化的调控机制
神经干细胞(NSCs)是一种在中枢神经系统中能够自我复制并分化为神经元和胶质细胞的细胞。海马齿状回(DG)的亚颗粒区(SGZ)和脑室下区(SVZ)是在成人大脑中发现NSCs的两个主要位置。最近在成年哺乳动物大脑中发现的NSCs引发了一系列临床前和转化研究,以研究治疗神经退行性疾病的新策略。因此,动员内源性NSCs已成为一种可能的脑修复治疗策略。松果体产生和释放的主要分泌物质是褪黑激素,具有广泛的生物学功能。褪黑素最近被证明在NSCs的增殖、分化和存活中起着重要作用。这些过程受到多种因素的调控,如MAPK/ERK信号通路、组蛋白乙酰化、神经营养因子和凋亡基因,本文将对这些因素进行讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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