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表观遗传学和氧化还原信号在肠-脑通讯中的潜在作用及自闭症谱系障碍案例

Potential Role of Epigenetics and Redox Signaling in the Gut-Brain Communication and the Case of Autism Spectrum Disorder.

作者信息

Doenyas Ceymi

机构信息

Yildiz Technical University, Istanbul, Turkey.

出版信息

Cell Mol Neurobiol. 2022 Mar;42(2):483-487. doi: 10.1007/s10571-021-01167-3. Epub 2021 Nov 13.

Abstract

The gut-brain axis refers to the bidirectional connection and communication between the gastrointestinal tract and the central nervous system. This paper explores two routes for this communication that have hitherto remained under-examined: epigenetics and redox signaling and their implications for autism spectrum disorder (ASD). The gut microbiota may induce epigenetic changes in the gut and potentially in the brain through their fermentation products. Instead of through other conceptualizations of them acting as neurotransmitters, gut microbial products may act as epigenetic agents, which are supported by the effects of gut bacterial-derived metabolites on gene regulation and expression. In addition to their epigenetic effects, gut bacterial-derived communicative agents can also influence host signaling by contributing to and even substituting host reactive oxygen species (ROS) production. These ROS can act as second messengers and exert oxidative activity on proteins to influence immune, inflammatory, and other signaling processes. ROS and epigenetic mechanisms may have interactive effects as well. ROS, in addition to their role in signaling pathways and cellular redox alterations, also influence redox-sensitive transcription factors, thereby having an effect on gene expression. Specifically, ROS are involved in the activation of transcription factors, chromatin remodeling, and histone/protein deacetylation. These two proposed mechanisms correspond with the recent findings related to ASD, where a cofactor that is shown to be lower in ASD has antioxidative properties, responds to epigenetic modulation, and increases via microbiota interventions. The current evidence reviewed here suggests the need to update models of the gut-brain communication to include these two mechanisms. Such a modeling can also contribute to understanding the unknowns of host metabolism and physiology in ASD and afford potential therapeutic avenues for this as well as other psychiatric and physiological conditions.

摘要

肠-脑轴是指胃肠道与中枢神经系统之间的双向连接和通信。本文探讨了迄今尚未得到充分研究的两种这种通信途径:表观遗传学和氧化还原信号传导及其对自闭症谱系障碍(ASD)的影响。肠道微生物群可能通过其发酵产物在肠道甚至可能在大脑中诱导表观遗传变化。肠道微生物产物可能作为表观遗传因子起作用,而不是通过它们作为神经递质的其他概念化方式,这得到了肠道细菌衍生代谢产物对基因调控和表达的影响的支持。除了表观遗传作用外,肠道细菌衍生的通信因子还可以通过促进甚至替代宿主活性氧(ROS)的产生来影响宿主信号传导。这些ROS可以作为第二信使,对蛋白质发挥氧化活性,以影响免疫、炎症和其他信号传导过程。ROS和表观遗传机制也可能具有相互作用。ROS除了在信号通路和细胞氧化还原改变中发挥作用外,还影响氧化还原敏感的转录因子,从而对基因表达产生影响。具体而言,ROS参与转录因子的激活、染色质重塑和组蛋白/蛋白质去乙酰化。这两种提出的机制与最近关于ASD的研究结果一致,其中一种在ASD中显示较低的辅助因子具有抗氧化特性,对表观遗传调节有反应,并通过微生物群干预增加。此处综述目前的证据表明,需要更新肠-脑通信模型以纳入这两种机制。这样的模型构建也有助于理解ASD中宿主代谢和生理学的未知因素,并为ASD以及其他精神和生理疾病提供潜在的治疗途径。

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