Epigenetic modulation of gene expression governs the brain's response to injury
被引:15
作者:
Simon, Roger P.
论文数: 0引用数: 0
h-index: 0
机构:
Morehouse Sch Med, Inst Neurosci, Translat Stroke Program, Atlanta, GA 30310 USA
Grady Mem Hosp, Atlanta, GA USAMorehouse Sch Med, Inst Neurosci, Translat Stroke Program, Atlanta, GA 30310 USA
Simon, Roger P.
[1
,2
]
机构:
[1] Morehouse Sch Med, Inst Neurosci, Translat Stroke Program, Atlanta, GA 30310 USA
Ischemia;
Seizure;
Neuroprotection;
Epigenetic regulation;
PcG proteins;
DNA methylation;
POLYCOMB GROUP PROTEINS;
TRANSIENT ISCHEMIC ATTACKS;
FOCAL CEREBRAL-ISCHEMIA;
STATUS EPILEPTICUS;
DNA METHYLATION;
CELL FATE;
ENDOGENOUS NEUROPROTECTION;
DYNAMIC REGULATION;
X-CHROMOSOME;
TOLERANCE;
D O I:
10.1016/j.neulet.2015.12.024
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Mild stress from ischemia, seizure, hypothermia, or infection can produce a transient neuroprotected state in the brain. In the neuroprotected state, the brain responds differently to a severe stress and sustains less injury. At the genomic level, the response of the neuroprotected brain to a severe stress is characterized by widespread differential regulation of genes with diverse functions. This reprogramming of gene expression observed in the neuroprotected brain in response to a stress is consistent with an epigenetic model of regulation mediated by changes in DNA methylation and histone modification. Here, we summarize our evolving understanding of the molecular basis for endogenous neuroprotection and review recent findings that implicate DNA methylation and protein mediators of histone modification as epigenetic regulators of the brain's response to injury. (C) 2015 Elsevier Ireland Ltd. All rights reserved.