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衰老和神经发生过程中的表观遗传机制,为人类大脑疾病的新型治疗途径。

Epigenetic mechanisms during ageing and neurogenesis as novel therapeutic avenues in human brain disorders.

机构信息

Cancer Epigenetics Group, Cancer Epigenetics and Biology Program (PEBC), Bellvitge Biomedical Biomedical Research Institute (IDIBELL), 3rd Floor, Hospital Duran i Reynals, Av. Gran Via 199-203, 08908L'Hospitalet, Barcelona, Catalonia Spain.

Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience (MHeNs), Maastricht University, Maastricht, The Netherlands.

出版信息

Clin Epigenetics. 2017 Jun 29;9:67. doi: 10.1186/s13148-017-0365-z. eCollection 2017.

Abstract

Ageing is the main risk factor for human neurological disorders. Among the diverse molecular pathways that govern ageing, epigenetics can guide age-associated decline in part by regulating gene expression and also through the modulation of genomic instability and high-order chromatin architecture. Epigenetic mechanisms are involved in the regulation of neural differentiation as well as in functional processes related to memory consolidation, learning or cognition during healthy lifespan. On the other side of the coin, many neurodegenerative diseases are associated with epigenetic dysregulation. The reversible nature of epigenetic factors and, especially, their role as mediators between the genome and the environment make them exciting candidates as therapeutic targets. Rather than providing a broad description of the pathways epigenetically deregulated in human neurological disorders, in this review, we have focused on the potential use of epigenetic enzymes as druggable targets to ameliorate neural decline during normal ageing and especially in neurological disorders. We will firstly discuss recent progress that supports a key role of epigenetic regulation during healthy ageing with an emphasis on the role of epigenetic regulation in adult neurogenesis. Then, we will focus on epigenetic alterations associated with ageing-related human disorders of the central nervous system. We will discuss examples in the context of psychiatric disorders, including schizophrenia and posttraumatic stress disorders, and also dementia or Alzheimer's disease as the most frequent neurodegenerative disease. Finally, methodological limitations and future perspectives are discussed.

摘要

衰老是人类神经紊乱的主要风险因素。在控制衰老的众多分子途径中,表观遗传学可以通过调节基因表达,以及通过调节基因组不稳定性和高阶染色质结构,在一定程度上指导与年龄相关的衰退。表观遗传机制参与神经分化的调控,以及在健康寿命期间与记忆巩固、学习或认知相关的功能过程。另一方面,许多神经退行性疾病与表观遗传失调有关。表观遗传因素的可逆性,特别是它们作为基因组和环境之间的中介的作用,使它们成为有希望的治疗靶点。本文不是广泛描述在人类神经紊乱中表观遗传失调的途径,而是重点讨论表观遗传酶作为改善正常衰老期间和神经紊乱中神经衰退的潜在治疗靶点。我们将首先讨论支持表观遗传调控在健康衰老中关键作用的最新进展,重点是表观遗传调控在成年神经发生中的作用。然后,我们将集中讨论与中枢神经系统衰老相关的人类疾病相关的表观遗传改变。我们将在精神疾病(包括精神分裂症和创伤后应激障碍)的背景下讨论一些例子,还将讨论痴呆症或阿尔茨海默病,因为它是最常见的神经退行性疾病。最后,讨论了方法学限制和未来展望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c23d/5493012/b5737e93cc60/13148_2017_365_Fig1_HTML.jpg

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