Therapeutic Potential of a Combination of Electroacupuncture and Human iPSC-Derived Small Extracellular Vesicles for Ischemic Stroke

被引:37
作者
Deng, Peiying [1 ]
Wang, Liang [2 ,3 ]
Zhang, Qiongqiong [1 ]
Chen, Suhui [1 ]
Zhang, Yamin [1 ]
Xu, Hong [1 ]
Chen, Hui [2 ,3 ]
Xu, Yi [2 ,3 ]
He, Wei [2 ,3 ]
Zhang, Jianmin [2 ,3 ,4 ,5 ]
Sun, Hua [1 ]
机构
[1] Chinese Acad Med Sci, Peking Union Med Coll, Peking Union Med Coll Hosp, Dept Tradit Chinese Med, Beijing 100730, Peoples R China
[2] Chinese Acad Med Sci, Inst Basic Med Sci, Dept Immunol, CAMS Key Lab T Cell & Immunotherapy,State Key Lab, Beijing 100005, Peoples R China
[3] Peking Union Med Coll, Sch Basic Med, Beijing 100005, Peoples R China
[4] Changzhou Xitaihu Inst Frontier Technol Cell Ther, Changzhou 213000, Peoples R China
[5] Guidon Pharmaceut, Beijing 100176, Peoples R China
基金
中国国家自然科学基金;
关键词
electroacupuncture; induced pluripotent stem cell; ischemic stroke; inflammation; IL-33; ST2; STEM-CELLS; FUNCTIONAL RECOVERY; REPERFUSION INJURY; CEREBRAL-ISCHEMIA; BRAIN-INJURY; IL-33; EXOSOMES; INTERLEUKIN-33; COLITIS; TIME;
D O I
10.3390/cells11050820
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
This paper aimed to explore the roles of the combination of electroacupuncture (EA) and induced pluripotent stem cell-derived small extracellular vesicles (iPSC-EVs) on mice with ischemic stroke and the underlying mechanisms. A focal cerebral ischemia model was established in C57BL/6 mice through middle cerebral artery occlusion (MCAO). After 3 days, neurological impairment and motor function were examined by performing behavioral tests. The infarct volume and neuronal apoptosis were examined using TTC staining and TUNEL assays. Flow cytometry was performed to assess the proliferation of T lymphocytes. The changes in the interleukin (IL)-33/ST2 axis were evaluated by immunofluorescence and Western blotting. The combination of EA and iPSC-EVs treatment ameliorated neurological impairments and reduced the infarct volume and neuronal apoptosis in MCAO mice. EA plus iPSC-EVs suppressed T helper (Th1) and Th17 responses and promoted the regulatory T cell (Treg) response. In addition, EA plus iPSC-EVs exerted neuroprotective effects by regulating the IL-33/ST2 axis and inhibiting the microglia and astrocyte activation. Taken together, the study shows that EA and iPSC-EVs exerted a synergistic neuroprotective effect in MCAO mice, and this treatment may represent a novel potent therapy for ischemic stroke and damage to other tissues.
引用
收藏
页数:17
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