Unraveling the epigenetic landscape of depression: focus on early life stress

被引:72
|
作者
Torres-Berrio, Angelica [1 ,2 ]
Issler, Orna [1 ,2 ]
Parise, Eric M. [1 ,2 ]
Nestler, Eric J. [1 ,2 ]
机构
[1] Icahn Sch Med Mt Sinai, Nash Family Dept Neurosci, One Gustave L Levy Pl,Box 1065, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Friedman Brain Inst, One Gustave L Levy Pl,Box 1065, New York, NY 10029 USA
关键词
chromatin remodeling; histone modification; DNA methylation; noncoding RNA; early life stress; MEDIAL PREFRONTAL CORTEX; DNA METHYLATION; MATERNAL-CARE; GLUCOCORTICOID-RECEPTOR; GENE-EXPRESSION; ADULT RATS; ADOLESCENT; ADVERSITY; VULNERABILITY; ALTERS;
D O I
10.31887/DCNS.2019.21.4/enestler
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Depression is a devastating psychiatric disorder caused by a combination of genetic predisposition and life events, mainly exposure to stress. Early life stress (ELS) in particular is known to "scar" the brain, leading to an increased susceptibility to developing depression later in life via epigenetic mechanisms. Epigenetic processes lead to changes in gene expression that are not due to changes in NA sequence, but achieved via modulation of chromatin modifications, NA methylation, and noncoding RNAs. Here we review common epigenetic mechanisms including the enzymes that take part in reading, writing, and erasing specific epigenetic marks. We then describe recent developments in understanding how ELS leads to changes in the epigenome that are manifested in increased susceptibility to depression-like abnormalities in animal models. We conclude with highlighting the need for future studies that will potentially enable the utilisation of the understanding of epigenetic changes linked to ELS for the development of much-needed novel therapeutic strategies and biomarker discovery. (C) 2019, AICH - Servier Group.
引用
收藏
页码:341 / 357
页数:17
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