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电针通过miR-191a-5p靶向神经元钙传感器1减轻缺血性中风后的脑损伤。

Electroacupuncture Alleviates Brain Damage Through Targeting of Neuronal Calcium Sensor 1 by miR-191a-5p After Ischemic Stroke.

作者信息

Zhou Heng, Yang Cen, Bai Fuhai, Ma Zhi, Wang Jingyi, Wang Feng, Li Feng, Wang Qiang, Xiong Lize

机构信息

1 Department of Anesthesiology, Xijing Hospital, Forth Military Medical University , Xi'an, China .

2 Department of Anesthesiology, The First Affiliated Hospital of Xi'an Jiaotong University , Xi'an, China .

出版信息

Rejuvenation Res. 2017 Dec;20(6):492-505. doi: 10.1089/rej.2017.1920. Epub 2017 Jul 17.

Abstract

Electroacupuncture (EA) administration before or after cerebral ischemia has been shown to afford protection against ischemic injury. However, the underlying mechanism of EA-mediated protection is still unclear. Functional microRNAs (miRNAs) are believed to play important roles in neuroprotection and synaptic plasticity during and after ischemia. In a previous study, we identified 20 miRNAs that are expressed in the penumbra and are significantly changed after EA treatment. Here, we used bioinformatic analysis to predict the biological functions and gene networks of these miRNAs. Consistent with our predictions, downregulation of miR-191a-5p in primary neurons and in cortexes of rats increased cell viability, decreased apoptosis, reduced infarct volumes, and improved neurological scores; whereas upregulation of miR-191a-5p exacerbated neuronal injury and partly reversed the neuroprotective effect of EA treatment after ischemia/reperfusion injury. In silico analysis predicted that miR-191a-5p targets neuronal calcium sensor 1 (NCS-1), brain-derived neurotrophic factor, and growth-associated protein 43 (GAP43), and using luciferase reporter assays, we confirmed that the NCS-1 3'UTR (untranslated region) is targeted by miR-191a-5p. Furthermore, lentivirus-mediated overexpression of NCS-1 in primary neurons and in the cortexes of rats induced neuroprotection, while lentivirus-mediated knockdown had the opposite effect. Taken together, these data suggest that miRNAs participate in the response to EA treatment after cerebral ischemia and further imply that NCS-1 may constitute a miR-191a-5p target gene and a potential therapeutic target for neuroprotection.

摘要

脑缺血前后进行电针治疗已被证明可对缺血性损伤起到保护作用。然而,电针介导保护作用的潜在机制仍不清楚。功能性微小RNA(miRNA)被认为在缺血期间及之后的神经保护和突触可塑性中发挥重要作用。在先前的一项研究中,我们鉴定出20种在半暗带表达且电针治疗后有显著变化的miRNA。在此,我们使用生物信息学分析来预测这些miRNA的生物学功能和基因网络。与我们的预测一致,在原代神经元和大鼠皮层中下调miR-191a-5p可提高细胞活力、减少细胞凋亡、减小梗死体积并改善神经功能评分;而在缺血/再灌注损伤后上调miR-191a-5p会加剧神经元损伤并部分逆转电针治疗的神经保护作用。计算机分析预测miR-191a-5p靶向神经元钙传感器1(NCS-1)、脑源性神经营养因子和生长相关蛋白43(GAP43),并且通过荧光素酶报告基因检测,我们证实NCS-1的3'非翻译区(UTR)是miR-191a-5p的靶标。此外,慢病毒介导的NCS-1在原代神经元和大鼠皮层中的过表达诱导了神经保护作用,而慢病毒介导的敲低则产生相反的效果。综上所述,这些数据表明miRNA参与了脑缺血后对电针治疗的反应,并进一步暗示NCS-1可能构成miR-191a-5p的靶基因以及神经保护的潜在治疗靶点。

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