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电针通过外泌体微小RNA 146b促进缺血性中风后内源性神经干细胞的分化。

Electro-Acupuncture Promotes the Differentiation of Endogenous Neural Stem Cells via Exosomal microRNA 146b After Ischemic Stroke.

作者信息

Zhang Shenghang, Jin Tingting, Wang Lulu, Liu Weilin, Zhang Yuhao, Zheng Yi, Lin Yunjiao, Yang Minguang, He Xiaojun, Lin Huawei, Chen Lidian, Tao Jing

机构信息

College of Rehabilitation Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou, China.

The 900 Hospital of the Joint Logistic Team, Fuzhou, China.

出版信息

Front Cell Neurosci. 2020 Jul 21;14:223. doi: 10.3389/fncel.2020.00223. eCollection 2020.

Abstract

Evidences indicate that exosomes-mediated delivery of microRNAs (miRNAs or miRs) is involved in the neurogenesis of stroke. This study was to investigate the role of exosomal miRNAs in non-drug therapy of electro-acupuncture (EA) regulating endogenous neural stem cells for stroke recovery. The model of focal cerebral ischemia and reperfusion in rats were established by middle cerebral artery occlusion (MCAO) and treated by EA. The exosomes were extracted from peri-ischemic striatum and identified by exosomal biomarkers, and detected differentially expressed miRNAs with microarray chip. Primary stem cells were cultured, and oxygen-glucose deprivation and reperfusion (OGD/R) was used to mimic vitro ischemic injury. The levels of exosomal biomarkers TSG101 and CD81 were increased in peri-ischemic striatum after EA treatment, and we revealed 25 differentially expressed miRNAs in isolated exosomes, of which miR-146b was selected for further analysis, and demonstrated that EA increased miR-146b expression and its inhibitors could block the effects. Subsequently, we confirmed that EA upregulated miR-146b expression to promote neural stem cells differentiation into neurons in peri-ischemic striatum. , it was verified that OGD/R hindered neural stem cells differentiation, and miR-146b inhibitors furtherly suppressed its differentiation, simultaneously NeuroD1 was involved in neural stem cells differentiation into neurons. Moreover, we found EA promoted NeuroD1-mediated neural stem cells differentiation via miR-146b. In addition, EA also could improve neurological deficits through miR-146b after ischemic stroke. EA promotes the differentiation of endogenous neural stem cells via exosomal miR-146b to improve neurological injury after ischemic stroke.

摘要

证据表明,外泌体介导的微小RNA(miRNA或miR)传递参与了中风后的神经发生。本研究旨在探讨外泌体miRNA在电针(EA)非药物治疗调节内源性神经干细胞促进中风恢复中的作用。通过大脑中动脉闭塞(MCAO)建立大鼠局灶性脑缺血再灌注模型,并给予EA治疗。从缺血周围纹状体中提取外泌体,通过外泌体生物标志物进行鉴定,并用微阵列芯片检测差异表达的miRNA。培养原代干细胞,采用氧糖剥夺再灌注(OGD/R)模拟体外缺血损伤。EA治疗后,缺血周围纹状体中外泌体生物标志物TSG101和CD81的水平升高,我们在分离的外泌体中发现了25种差异表达的miRNA,其中选择miR-146b进行进一步分析,并证明EA增加了miR-146b的表达,其抑制剂可阻断其作用。随后,我们证实EA上调miR-146b表达以促进缺血周围纹状体中的神经干细胞分化为神经元。此外,证实OGD/R阻碍神经干细胞分化,miR-146b抑制剂进一步抑制其分化,同时NeuroD1参与神经干细胞向神经元的分化。此外,我们发现EA通过miR-146b促进NeuroD1介导的神经干细胞分化。另外,缺血性中风后EA还可通过miR-146b改善神经功能缺损。EA通过外泌体miR-146b促进内源性神经干细胞分化,以改善缺血性中风后的神经损伤。

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