Rosete Cal, Ciernia Annie Vogel
Djavad Mowafaghian Centre for Brain Health, Vancouver, V6T 1Z3, Canada.
Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, V6T 2A1, Canada.
Epigenomics. 2024 Nov-Nov;16(21-22):1373-1388. doi: 10.1080/17501911.2024.2419357. Epub 2024 Nov 8.
Histone deacetylase 3 (HDAC3) is a critical regulator of gene expression, influencing a variety of cellular processes in the central nervous system. As such, dysfunction of this enzyme may serve as a key driver in the pathophysiology of various neuropsychiatric disorders and neurodegenerative diseases. HDAC3 plays a crucial role in regulating neuroinflammation, and is now widely recognized as a major contributor to neurological conditions, as well as in promoting neuroprotective recovery following brain injury, hemorrhage and stroke. Emerging evidence suggests that pharmacological inhibition of HDAC3 can mitigate behavioral and neuroimmune deficits in various brain diseases and disorders, offering a promising therapeutic strategy. Understanding HDAC3 in the healthy brain lays the necessary foundation to define and resolve its dysfunction in a disease state. This review explores the mechanisms of HDAC3 in various cell types and its involvement in disease pathology, emphasizing the potential of HDAC3 inhibition to address neuroimmune, gene expression and behavioral deficits in a range of neurodegenerative and neuropsychiatric conditions.
组蛋白去乙酰化酶3(HDAC3)是基因表达的关键调节因子,影响中枢神经系统中的多种细胞过程。因此,这种酶的功能障碍可能是各种神经精神疾病和神经退行性疾病病理生理学的关键驱动因素。HDAC3在调节神经炎症中起关键作用,目前已被广泛认为是神经系统疾病的主要促成因素,以及在促进脑损伤、出血和中风后的神经保护恢复中起关键作用。新出现的证据表明,HDAC3的药理学抑制可以减轻各种脑部疾病和障碍中的行为和神经免疫缺陷,提供了一种有前景的治疗策略。了解健康大脑中的HDAC3为定义和解决其在疾病状态下的功能障碍奠定了必要的基础。本综述探讨了HDAC3在各种细胞类型中的机制及其在疾病病理学中的作用,强调了HDAC3抑制在一系列神经退行性和神经精神疾病中解决神经免疫、基因表达和行为缺陷的潜力。