MiR-145 enriched exosomes derived from bone marrow-derived mesenchymal stem cells protects against cerebral ischemia-reperfusion injury through downregulation of FOXO1

• Published in: Biochemical and biophysical research communications Vol. 632; pp. 92 - 99
• Main Authors: Zhou, Hai, Zhou, Jing, Teng, Hongwei, Yang, Hua, Qiu, Jinsong, Li, Xiangdong
• Format: Journal Article
• Language: English
• Published: Elsevier Inc 03.12.2022
• Subjects: animal models; apoptosis; bone marrow; brain; brain damage; BV2 cells; cell communication; cell cycle checkpoints; Exosomes; infarction; ischemia; Ischemic stroke; Mesenchymal stem cells; microRNA; neuroglia; oxidative stress; phenotype; stroke; BV2 cells; microRNA; Ischemic stroke; Exosomes; Mesenchymal stem cells
• DOI: 10.1016/j.bbrc.2022.09.089
• ISSN: 0006-291X; 1090-2104

Mesenchymal stem cells-derived exosomes (MSCs-Exo) were able to exert neuroprotective effects in brain injury after ischemic stroke (IS). In addition, exosomes containing microRNAs (miRNAs) can be transported to recipient cells to mediate intercellular communication. It has been shown that the level of miR-145 was significantly downregulated in brain tissues of rats subjected to middle cerebral artery occlusion (MCAO). However, the role of MSCs-derived exosomal miR-145 in IS progression remains largely unknown. Microglial BV2 cell exposed to oxygen-glucose deprivation/reperfusion (OGD/R) was applied to mimic cerebral ischemia/reperfusion (I/R) injury conditions in vitro. In addition, a rat model of MCAO was established to induce I/R injury. Meanwhile, exosomes were isolated from miR-145-transfected bone marrow MSCs, and then these isolated exosomes were used to treat OGD/R-stimulated BV-2 cell and rats subject to MCAO/R. In this study, we found that miR-145 could be transferred from MSCs to BV2 cells via exosomes. In addition, exosomal miR-145-derived from MSCs was able to shift microglia polarization toward anti-inflammatory M2 phenotype in OGD/R-stimulated BV2 cells. Moreover, exosomal miR-145 markedly suppressed the apoptosis, cell cycle arrest and oxidative stress in OGD/R-treated BV2 cells. Additionally, exosomal miR-145 notably decreased the expression of FOXO1 in BV2 cell exposed to OGD/R and in brain tissues of MCAO rats. Furthermore, exosomal miR-145 remarkably decreased infarct area in MCAO rats. Collectively, exosomal miR-145-derived from MSCs was able to attenuate cerebral I/R injury through downregulation of FOXO1. These studies may serve as a potential approach for treating of cerebral I/R injury. •MiR-145 could be transferred from MSCs to BV2 cells via exosomes.•Exosomal miR-145 regulated microglial polarization to prevent I/R injury.•Exosomal miR-145 could reduce infarct area in MCAO rats.•Exosomal miR-145 attenuated cerebral I/R injury via inhibiting FOXO1.