Epigenetic Regulation of Neural Stem Cells in Developmental and Adult Stages

被引:0
|
作者
Kunoh, Shu [1 ]
Nakashima, Hideyuki [1 ]
Nakashima, Kinichi [1 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Stem Cell Biol & Med, Fukuoka 8128582, Japan
基金
日本学术振兴会;
关键词
neural stem cells; epigenetics; brain; development; neurogenesis; astrogenesis; chromatin; DNA METHYLATION; HIPPOCAMPAL NEUROGENESIS; HISTONE METHYLTRANSFERASE; NEURONAL DIFFERENTIATION; ALZHEIMERS-DISEASE; ALPHA-SYNUCLEIN; GENE-EXPRESSION; RETT-SYNDROME; SELF-RENEWAL; CHROMATIN MODIFICATIONS;
D O I
10.3390/epigenomes8020022
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The development of the nervous system is regulated by numerous intracellular molecules and cellular signals that interact temporally and spatially with the extracellular microenvironment. The three major cell types in the brain, i.e., neurons and two types of glial cells (astrocytes and oligodendrocytes), are generated from common multipotent neural stem cells (NSCs) throughout life. However, NSCs do not have this multipotentiality from the beginning. During cortical development, NSCs sequentially obtain abilities to differentiate into neurons and glial cells in response to combinations of spatiotemporally modulated cell-intrinsic epigenetic alterations and extrinsic factors. After the completion of brain development, a limited population of NSCs remains in the adult brain and continues to produce neurons (adult neurogenesis), thus contributing to learning and memory. Many biological aspects of brain development and adult neurogenesis are regulated by epigenetic changes via behavioral control of NSCs. Epigenetic dysregulation has also been implicated in the pathogenesis of various brain diseases. Here, we present recent advances in the epigenetic regulation of NSC behavior and its dysregulation in brain disorders.
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页数:20
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