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慢性社交隔离导致雄性小鼠通过海马 METTL14 介导的 RNA m6A 修饰的表观转录组异常行为。

Chronic social isolation leads to abnormal behavior in male mice through the hippocampal METTL14 mediated epitranscriptomic RNA m6A modifications.

机构信息

Clinical Anatomy & Reproductive Medicine Application Institute, Hengyang Medical School, University of South China, Hengyang, Hunan 421001, China; Department of Neurosurgery, Liaocheng People's Hospital, Liaocheng 252000, Shandong, China.

Clinical Anatomy & Reproductive Medicine Application Institute, Hengyang Medical School, University of South China, Hengyang, Hunan 421001, China.

出版信息

J Affect Disord. 2024 Dec 1;366:262-272. doi: 10.1016/j.jad.2024.08.173. Epub 2024 Aug 27.

Abstract

BACKGROUND

Social isolation not only increases the risk of mortality in later life but also causes depressive symptoms, cognitive and physical disabilities. Although RNA m6A modifications are suggested to play key roles in brain development, neuronal signaling and neurological disorders, both the roles of m6A and the enzymes that regulate RNA m6A modification in social isolation induced abnormal behavior is unknown. The present study aims to explore the possible epitranscriptomic role of RNA m6A modifications and its enzymes in social isolation induced impaired behavior.

METHODS

3-4 weeks mice experiencing 8 weeks social isolation stress (SI) were used in the present study. We quantified m6A levels in brain regions related to mood and cognitive behavior. And the expression of hippocampal m6A enzymes was also determined. The role of hippocampal m6A and its enzymes in SI induced abnormal behavior was further verified by the virus tool.

RESULTS

SI led to not only depressive and anxiety-like behaviors but also cognitive impairment, with corresponding decreases in hippocampal m6A and METTL14. Hippocampal over-expression METTL14 with lentivirus not only rescued these behaviors but also enhanced the hippocampal m6A level. Hippocampal over-expression METTL14 resulted in increased synaptic related genes.

CONCLUSIONS

We provide the first evidence that post-weaning social isolation reduces hippocampal m6A level and causes altered expression of m6A enzyme in mice. Importantly, hippocampal METTL14 over-expression alleviated the SI-induced depression/anxiety-like and impaired cognitive behaviors and enhanced m6A level and synaptic related genes expression.

摘要

背景

社交隔离不仅会增加晚年的死亡率,还会导致抑郁症状、认知和身体残疾。尽管 RNA m6A 修饰被认为在大脑发育、神经元信号和神经紊乱中发挥关键作用,但 m6A 的作用及其调节 RNA m6A 修饰的酶在社交隔离引起的异常行为中的作用尚不清楚。本研究旨在探讨 RNA m6A 修饰及其酶在社交隔离引起的行为障碍中的潜在表转录组学作用。

方法

本研究使用经历了 8 周社交隔离应激(SI)的 3-4 周龄小鼠。我们定量了与情绪和认知行为相关的大脑区域中的 m6A 水平。并确定了海马体中 m6A 酶的表达。通过病毒工具进一步验证了海马体 m6A 及其酶在 SI 诱导的异常行为中的作用。

结果

SI 不仅导致抑郁和焦虑样行为,还导致认知障碍,同时伴随着海马体 m6A 和 METTL14 的减少。用慢病毒过表达 METTL14 不仅挽救了这些行为,还增强了海马体的 m6A 水平。海马体过表达 METTL14 导致突触相关基因增加。

结论

我们提供了第一个证据,即婴儿期后社交隔离会降低海马体 m6A 水平,并导致小鼠中 m6A 酶表达改变。重要的是,海马体 METTL14 的过表达缓解了 SI 引起的抑郁/焦虑样和认知障碍行为,并增强了 m6A 水平和突触相关基因的表达。

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