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Signal transduction and epigenetic mechanisms in the control of microglia activation during neuroinflammation

机译:控制神经炎症过程中小胶质细胞活化的信号转导和表观遗传机制

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摘要

Activation of microglia is a common denominator and a pathophysiological hallmark of the central nervous system (CNS) disorders. Damage or CNS disorders can trigger inflammatory responses in resident microglia and initiate a systemic immune system response. Although a repertoire of inflammatory responses differs in those diseases, there is a spectrum of transcriptionally activated genes that encode various mediators such as growth factors, inflammatory cytokines, chemokines, matrix metalloproteinases, enzymes producing lipid mediators, toxic molocules, all of which contribute to neuroinflammation. The initiation, progression and termination of inflammation requires global activation of gene expression, postranscriptional regulation, epigenetic modifications, changes in chromatin structure and these processes are tightly regulated by specific signaling pathways. This review focuses on the function of "master regulators" and epigenetic mechanisms in microglia activation during neuroinflammation. We review studies showing impact of epigenetic enzyme inhibitors on microglia activation in vitro and in vivo, and critically discuss potential of such molecules to prevent/moderate pathological events mediated by microglia under brain pathologies. This article is part of a Special Issue entitled: Neuro Inflammation edited by Helga E. de Vries and Markus Schwaninger. (C) 2015 Elsevier B.V. All rights reserved.
机译:小胶质细胞的激活是中枢神经系统(CNS)疾病的共同点和病理生理学标志。损伤或中枢神经系统疾病可触发常驻小胶质细胞的炎症反应,并引发全身性免疫系统反应。尽管在这些疾病中炎症反应的方式有所不同,但仍有一系列转录激活的基因编码各种介质,例如生长因子,炎症细胞因子,趋化因子,基质金属蛋白酶,产生脂质介质的酶,毒性分子,所有这些都与神经炎症有关。 。炎症的发生,发展和终止需要基因表达的整体激活,转录后调控,表观遗传修饰,染色质结构改变,而这些过程受特定信号通路的严格调控。这篇综述集中在神经炎症过程中小胶质细胞活化中的“主调节剂”的功能和表观遗传机制。我们审查研究表明表观遗传酶抑制剂在体外和体内对小胶质细胞活化的影响,并严格讨论这种分子在脑病理学下预防/减轻由小胶质细胞介导的病理事件的潜力。本文是Helga E. de Vries和Markus Schwaninger编辑的题为:神经炎症的特刊的一部分。 (C)2015 Elsevier B.V.保留所有权利。

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