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微小RNA-7/支架蛋白3轴参与精神分裂症的发病机制。

MicroRNA-7/Shank3 axis involved in schizophrenia pathogenesis.

作者信息

Zhang Jin, Sun Xin-Yang, Zhang Li-Yi

机构信息

School of Medicine, Jiangsu University, Jiangsu, People's Republic of China.

Department of Psychology and Psychiatry, PingAn Health Cloud Company Ltd. of China, Shanghai 20050, People's Republic of China.

出版信息

J Clin Neurosci. 2015 Aug;22(8):1254-7. doi: 10.1016/j.jocn.2015.01.031. Epub 2015 Apr 14.

Abstract

This study aimed to identify the difference of microRNA-7 (miR-7) expression levels between schizophrenia patients and healthy controls and to investigate the regulatory effects of miR-7 on the SHANK3 gene in schizophrenia. miR-7 levels in plasma were detected by quantitative polymerase chain reactions (qPCR) in 50 schizophrenia patients and 50 healthy controls. The hippocampal neuron cell line, HT22, was transfected with lentiviral vector overexpressing or knocking-down miR-7, and the expression levels of SHANK3 mRNA and Shank3 protein were measured by qPCR and immunofluorescence. A luciferase assay was carried out to analyze the regulatory effects of miR-7 on SHANK3. Circulating miR-7 level was significantly increased in schizophrenia patients (p = 0.022). Overexpression of miR-7 suppressed the expression of SHANK3 while the levels of SHANK3 mRNA and Shank protein were significantly increased by miR-7 knockdown. We conclude that miR-7 binds to 3-prime untranslated regions of SHANK3 mRNA and causes the alteration of neuronal morphology and function, potentially playing a crucial role in the pathophysiological process of schizophrenia.

摘要

本研究旨在确定精神分裂症患者与健康对照者之间微小RNA-7(miR-7)表达水平的差异,并研究miR-7对精神分裂症中SHANK3基因的调控作用。采用定量聚合酶链反应(qPCR)检测了50例精神分裂症患者和50例健康对照者血浆中的miR-7水平。用表达或敲低miR-7的慢病毒载体转染海马神经元细胞系HT22,通过qPCR和免疫荧光检测SHANK3 mRNA和Shank3蛋白的表达水平。进行荧光素酶测定以分析miR-7对SHANK3的调控作用。精神分裂症患者的循环miR-7水平显著升高(p = 0.022)。miR-7过表达抑制了SHANK3的表达,而敲低miR-7则使SHANK3 mRNA和Shank蛋白水平显著升高。我们得出结论,miR-7与SHANK3 mRNA的3'非翻译区结合,导致神经元形态和功能改变,可能在精神分裂症的病理生理过程中起关键作用。

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