Bone Marrow Mesenchymal Stem Cells-derived Exosomal Long Non-coding RNA KLF3 antisense RNA 1 Enhances Autophagy to Protect Against Cerebral Ischemia/Reperfusion Injury Via ETS Variant Transcription Factor 4/Silent Information Regulator 1 Axis

被引：8
作者：
Xu, Qian [1 ]
Zhou, Dingzhou [2 ]
Yu, Dan [1 ]
机构：
[1] Cent South Univ, Haikou City Peoples Hosp, Xiangya Sch Med, Dept Neurol, Haikou 57020, Hainan, Peoples R China
[2] Hunan Normal Univ, Dept Neurosurg, Hunan Prov Peoples Hosp, Affiliated Hosp 1, Changsha 410000, Hunan, Peoples R China
来源：
NEUROSCIENCE | 2023年 / 521卷
基金：
中国国家自然科学基金;
关键词：
bone marrow mesenchymal stem cells; exosomes; cerebral ischemia; reperfusion injury; lncRNA KLF3-AS1; ETV4; Sirt1; ISCHEMIC-STROKE; INFLAMMATION;
D O I：
10.1016/j.neuroscience.2023.02.021
中图分类号：
Q189 [神经科学];
学科分类号：
071006 ;
摘要：
stem cells (MSCs)-derived exosomes are demonstrated to exert neuroprotective effects in stroke. We aimed to explore the role and mechanism of long non-coding RNA (lncRNA) KLF3 antisense RNA 1 (KLF3-AS1) in bone marrow mesenchymal stem cells-derived exosomes (BMSCs-Exos) in cerebral ischemia/ reperfusion (I/R) injury. Exosomes were isolated from the culture medium of BMSCs. A mouse model of middle cerebral artery occlusion (MCAO) in vivo and a BV-2 cell model of oxygen and glucose deprivation/reoxygenation (OGD/RX) in vitro were established. Cell viability and apoptosis were detected using MTT assay, TUNEL staining and flow cytometry, respectively. Related proteins were determined with western blot and immunohistochemistry, while related RNAs were analyzed by RT-qPCR. Neurological deficit and cerebral infarct volume were evaluated by the modified neurological severity score (mNSS) and TTC staining, respectively. Our observations indicate that exosomes derived from BMSCs-preconditioned medium exerted neuroprotective effects, as indicated by the increased cell viability and the suppressed apoptosis in OGD/RX-suffered BV-2 cells. KLF3-AS1 expression was upregulated in BMSCs-Exos. Furthermore, KLF3-AS1 knockdown antagonized the protective effects of BMSCs-Exos. Mechanistically, BMSCs-Exos carrying KLF3-AS1 inhibited apoptosis via enhancing autophagy. KLF3-AS1 was found to recruit ETS variant transcription factor 4 (ETV4), which upregulated Sirt1 expression. Knockdown of KLF3-AS1 neutralized the protective effects of BMSCs-Exos on MCAO-induced brain injury, which was then reversed by the treatment with Sirt1 inhibitor EX527. We concluded that KLF3-AS1 derived from BMSCs-Exos promoted autophagy to alleviate I/R injury via ETV4/Sirt1 axis. (c) 2023 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码：44 / 57
页数：14
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