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Advanced glycation end products inhibit neural stem cell differentiation via upregualtion of HDAC3 expression.晚期糖基化终产物通过上调 HDAC3 表达抑制神经干细胞分化。
Brain Res Bull. 2020 Jun;159:1-8. doi: 10.1016/j.brainresbull.2020.03.001. Epub 2020 Mar 3.
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BDNF as a Promising Therapeutic Agent in Parkinson's Disease.BDNF 作为治疗帕金森病的有希望的治疗剂。
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Neuroprotective Effects of Selective Inhibition of Histone Deacetylase 3 in Experimental Stroke.选择性抑制组蛋白去乙酰化酶 3 在实验性脑卒中的神经保护作用。
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Regulation of Central Nervous System Development by Class I Histone Deacetylases.I 类组蛋白去乙酰化酶对中枢神经系统发育的调控。
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Pharmacological intervention of histone deacetylase enzymes in the neurodegenerative disorders.组蛋白去乙酰化酶在神经退行性疾病中的药物干预。
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Epigenetic mechanisms in schizophrenia and other psychotic disorders: a systematic review of empirical human findings.精神分裂症和其他精神病障碍中的表观遗传机制:对经验性人类研究结果的系统综述。
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Histone deacetylases 1, 2 and 3 in nervous system development.组蛋白去乙酰化酶 1、2 和 3 在神经系统发育中的作用。
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The Bdnf and Npas4 genes are targets of HDAC3-mediated transcriptional repression.Bdnf 和 Npas4 基因是 HDAC3 介导的转录抑制的靶标。
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The Impact of Kinases in Amyotrophic Lateral Sclerosis at the Neuromuscular Synapse: Insights into BDNF/TrkB and PKC Signaling.激酶在神经肌肉突触中的肌萎缩性侧索硬化症中的作用:对 BDNF/TrkB 和 PKC 信号的深入了解。
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Environmental enrichment prevents Aβ oligomer-induced synaptic dysfunction through mirna-132 and hdac3 signaling pathways.环境富集通过 mirna-132 和 hdac3 信号通路预防 Aβ 寡聚体诱导的突触功能障碍。
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组蛋白去乙酰化酶-3:大脑的朋友和敌人。

Histone deacetylase-3: Friend and foe of the brain.

机构信息

Neugeneron, Dallas, TX 75243, USA.

出版信息

Exp Biol Med (Maywood). 2020 Jul;245(13):1130-1141. doi: 10.1177/1535370220928278. Epub 2020 Jun 2.

DOI:10.1177/1535370220928278
PMID:32486848
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7400723/
Abstract

Brain development and degeneration are highly complex processes that are regulated by a large number of molecules and signaling pathways the identities of which are being unraveled. Accumulating evidence points to histone deacetylases and epigenetic mechanisms as being important regulators of these processes. In this review, we describe that histone deacetylase-3 (HDAC3) is a particularly crucial regulator of both neurodevelopment and neurodegeneration. In addition, HDAC3 regulates memory formation, synaptic plasticity, and the cognitive impairment associated with normal aging. Understanding how HDAC3 functions contributes to the normal development and functioning of the brain while also promoting neurodegeneration could lead to the development of therapeutic approaches for neurodevelopmental, neuropsychiatric, and neurodegenerative disorders.

摘要

大脑发育和退化是高度复杂的过程,受大量分子和信号通路的调控,这些分子和信号通路的特性正在被逐步揭示。越来越多的证据表明组蛋白去乙酰化酶和表观遗传机制是这些过程的重要调节因子。在这篇综述中,我们描述了组蛋白去乙酰化酶-3(HDAC3)是神经发育和神经退行性变的一个特别关键的调节因子。此外,HDAC3 还调节记忆形成、突触可塑性以及与正常衰老相关的认知障碍。了解 HDAC3 的功能不仅有助于大脑的正常发育和功能,还可能导致神经发育、神经精神和神经退行性疾病治疗方法的发展。