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Transcriptional and Epigenetic Regulation in Injury-Mediated Neuronal Dendritic Plasticity

机译:损伤介导的神经元树突可塑性的转录和表观遗传调控。

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摘要

Injury to the nervous system induces localized damage in neural structures and neuronal death through the primary insult, as well as delayed atrophy and impaired plasticity of the delicate dendritic fields necessary for interneuronal communication. Excitotoxicity and other secondary biochemical events contribute to morphological changes in neurons following injury. Evidence suggests that various transcription factors are involved in the dendritic response to injury and potential therapies. Transcription factors play critical roles in the intracellular regulation of neuronal morphological plasticity and dendritic growth and patterning. Mounting evidence supports a crucial role for epigenetic modifications via histone deacetylases, histone acetyltransferases, and DNA methyltransferases that modify gene expression in neuronal injury and repair processes. Gene regulation through epigenetic modification is of great interest in neurotrauma research, and an early picture is beginning to emerge concerning how injury triggers intracellular events that modulate such responses. This review provides an overview of injury-mediated influences on transcriptional regulation through epigenetic modification, the intracellular processes involved in the morphological consequences of such changes, and potential approaches to the therapeutic manipulation of neuronal epigenetics for regulating gene expression to facilitate growth and signaling through dendritic arborization following injury.
机译:对神经系统的损伤会通过原发性损伤引起神经结构的局部损伤和神经元死亡,以及延迟神经萎缩和削弱神经元间交流所必需的脆弱的树突状区域的可塑性。兴奋性毒性和其他继发性生化事件会导致损伤后神经元的形态变化。有证据表明,各种转录因子参与了对损伤和潜在疗法的树突反应。转录因子在细胞内调节神经元形态可塑性和树突状生长和模式中起关键作用。越来越多的证据表明,通过在神经元损伤和修复过程中修饰基因表达的组蛋白脱乙酰基酶,组蛋白乙酰基转移酶和DNA甲基转移酶,对表观遗传修饰起着至关重要的作用。通过表观遗传修饰进行基因调控在神经创伤研究中引起了极大的兴趣,关于损伤如何触发细胞内事件调节这些反应的早期研究开始浮出水面。这篇综述概述了损伤介导的通过表观遗传修饰对转录调控的影响,涉及这种变化的形态学后果的细胞内过程以及神经元表观遗传学治疗性调控基因表达以促进通过树突生长和信号传导的潜在治疗方法。受伤后进行乔装。

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