Epigenetic modulation of gene expression governs the brain's response to injury

被引:15
作者
Simon, Roger P. [1 ,2 ]
机构
[1] Morehouse Sch Med, Inst Neurosci, Translat Stroke Program, Atlanta, GA 30310 USA
[2] Grady Mem Hosp, Atlanta, GA USA
关键词
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.
引用
收藏
页码:16 / 19
页数:4
相关论文
共 54 条
  • [1] Effects of lipopolysaccharide priming on acute ischemic brain injury
    Ahmed, SH
    He, YY
    Nassief, A
    Xu, J
    Xu, XM
    Hsu, CY
    [J]. STROKE, 2000, 31 (01) : 193 - 199
  • [2] Cellular memory and dynamic regulation of polycomb group proteins
    Bantignies, F
    Cavalli, G
    [J]. CURRENT OPINION IN CELL BIOLOGY, 2006, 18 (03) : 275 - 283
  • [3] Ischemic preconditioning and brain tolerance - Temporal histological and functional outcomes, protein synthesis requirement, and interleukin-1 receptor antagonist and early gene expression
    Barone, FC
    White, RF
    Spera, PA
    Ellison, J
    Currie, RW
    Wang, XK
    Feuerstein, GZ
    [J]. STROKE, 1998, 29 (09) : 1937 - 1950
  • [4] MOVEMENT OF THE X-CHROMOSOME IN EPILEPSY
    BORDEN, J
    MANUELIDIS, L
    [J]. SCIENCE, 1988, 242 (4886) : 1687 - 1691
  • [5] Increase in endogenous brain superoxide dismutase as a potential mechanism of lipopolysaccharide-induced brain ischemic tolerance
    Bordet, R
    Deplanque, D
    Maboudou, P
    Puisieux, F
    Pu, Q
    Robin, E
    Martin, A
    Bastide, M
    Leys, D
    Lhermitte, M
    Dupuis, B
    [J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2000, 20 (08) : 1190 - 1196
  • [6] Prevention from hypoxia-induced apoptosis by pre-conditioning:: a mechanistic approach in cultured neurons from fetal rat forebrain
    Bossenmeyer-Pourié, C
    Daval, JL
    [J]. MOLECULAR BRAIN RESEARCH, 1998, 58 (1-2): : 237 - 239
  • [7] Genome-wide mapping of Polycomb target genes unravels their roles in cell fate transitions
    Bracken, AP
    Dietrich, N
    Pasini, D
    Hansen, KH
    Helin, K
    [J]. GENES & DEVELOPMENT, 2006, 20 (09) : 1123 - 1136
  • [8] Role of Bmi-1 and Ring1A in H2A ubiquitylation and Hox gene silencing
    Cao, R
    Tsukada, Y
    Zhang, Y
    [J]. MOLECULAR CELL, 2005, 20 (06) : 845 - 854
  • [9] The Polycomb Group Gene Bmi1 Regulates Antioxidant Defenses in Neurons by Repressing p53 Pro-Oxidant Activity
    Chatoo, Wassim
    Abdouh, Mohamed
    David, Jocelyn
    Champagne, Marie-Pier
    Ferreira, Jose
    Rodier, Francis
    Bernier, Gilbert
    [J]. JOURNAL OF NEUROSCIENCE, 2009, 29 (02) : 529 - 542
  • [10] Stress proteins and tolerance to focal cerebral ischemia
    Chen, J
    Graham, SH
    Zhu, RL
    Simon, RP
    [J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1996, 16 (04) : 566 - 577