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与循环微小RNA谱相关的血清代谢组学揭示了miR-383-5p在模拟微重力下大鼠海马体中的作用。

Serum Metabolomics Associating With Circulating MicroRNA Profiles Reveal the Role of miR-383-5p in Rat Hippocampus Under Simulated Microgravity.

作者信息

Zhang Hongyu, Chen Jian, Wang Hailong, Lu Xin, Li Kai, Yang Chao, Wu Feng, Xu Zihan, Nie Huan, Ding Bai, Guo Zhifeng, Li Yu, Wang Jinfu, Li Yinghui, Dai Zhongquan

机构信息

State Key Laboratory of Space Medicine Fundamentals and Application, China Astronaut Research and Training Center, Beijing, China.

Institute of Cell and Developmental Biology, College of Life Sciences, Zhejiang University, Hangzhou, China.

出版信息

Front Physiol. 2020 Aug 18;11:939. doi: 10.3389/fphys.2020.00939. eCollection 2020.

Abstract

Microgravity impacts various aspects of human health. Yet the mechanisms of spaceflight-induced health problems are not elucidated. Here, we mapped the fusion systemic analysis of the serum metabolome and the circulating microRNAome in a hindlimb unloading rat model to simulate microgravity. The response of serum metabolites and microRNAs to simulated microgravity was striking. Integrated pathway analysis of altered serum metabolites and target genes of the significantly altered circulating miRNAs with Integrated Molecular Pathway-Level Analysis (IMPaLA) software was mainly suggestive of modulation of neurofunctional signaling pathways. Particularly, we revealed significantly increased miR-383-5p and decreased aquaporin 4 (AQP4) in the hippocampus. Using rabies virus glycoprotein-modified exosomes, delivery of miR-383-5p inhibited the expression of AQP4 not only in rat C6 glioma cells but also in the hippocampus . Using bioinformatics to map the crosstalk between the circulating metabolome and miRNAome could offer opportunities to understand complex biological systems under microgravity. Our present results suggested that the change of miR-383-5p level and its regulation of target gene AQP4 was one of the potential molecular mechanisms of microgravity-induced cognitive impairment in the hippocampus.

摘要

微重力会影响人类健康的各个方面。然而,太空飞行引发健康问题的机制尚未阐明。在此,我们在一个后肢卸载大鼠模型中进行了血清代谢组和循环微小RNA组的融合系统分析,以模拟微重力。血清代谢物和微小RNA对模拟微重力的反应十分显著。使用综合分子通路水平分析(IMPaLA)软件对血清代谢物改变以及循环微小RNA显著改变的靶基因进行综合通路分析,主要提示神经功能信号通路受到了调节。特别地,我们发现海马体中miR-383-5p显著增加,水通道蛋白4(AQP4)减少。利用狂犬病病毒糖蛋白修饰的外泌体,miR-383-5p的传递不仅抑制了大鼠C6胶质瘤细胞中AQP4的表达,也抑制了海马体中AQP4的表达。利用生物信息学来描绘循环代谢组和微小RNA组之间的相互作用,可能为理解微重力条件下的复杂生物系统提供机会。我们目前的结果表明,miR-383-5p水平的变化及其对靶基因AQP4的调控是微重力诱导海马体认知障碍的潜在分子机制之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6f1/7461998/068eef337520/fphys-11-00939-g001.jpg

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