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

被引:69
作者
Zhang, Shenghang [1 ,2 ]
Jin, Tingting [1 ]
Wang, Lulu [1 ]
Liu, Weilin [3 ]
Zhang, Yuhao [1 ]
Zheng, Yi [1 ]
Lin, Yunjiao [1 ]
Yang, Minguang [3 ]
He, Xiaojun [1 ]
Lin, Huawei [1 ]
Chen, Lidian [1 ]
Tao, Jing [1 ]
机构
[1] Fujian Univ Tradit Chinese Med, Coll Rehabil Med, Fuzhou, Peoples R China
[2] 900 Hosp Joint Logist Team, Fuzhou, Peoples R China
[3] Fujian Univ Tradit Chinese Med, Acad Rehabil Ind, Fuzhou, Peoples R China
关键词
electro-acupuncture; ischemic stroke; neural stem cells; exosomes; MiR-146b; CEREBRAL-ISCHEMIA; PROGENITOR CELLS; PROLIFERATION; NEUROGENESIS; RATS; ACTIVATION; NEURONS; MIGRATE; INJURY; BRAINS;
D O I
10.3389/fncel.2020.00223
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: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. Methods: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. Results: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.In vitro, 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,in vivowe 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. Conclusion:EA promotes the differentiation of endogenous neural stem cells via exosomal miR-146b to improve neurological injury after ischemic stroke.
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页数:11
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