间充质干细胞
微泡
STAT蛋白
细胞生物学
化学
外体
车站3
小RNA
祖细胞
信号转导
癌症研究
干细胞
生物
生物化学
基因
作者
Zhifeng Jiang,Yiru Shao,Lin Zhang,Jie Shen
摘要
Abstract Phosgene may induce acute lung injury (ALI) when a person is exposed to it. Mesenchymal stem cells (MSCs) were affirmed to have therapeutic effects on phosgene‐induced ALI. In a previous study, ALI exosomes have been confirmed to promote the proliferation and migration of MSCs. However, the mechanism of this phenomenon is still unclear. MicroRNAs (miRNAs) are essential in the physiological process of cells. In this study, lung‐derived exosomes were isolated from phosgene‐exposed and normal rats, respectively, through ultracentrifugation and cultured MSCs with these exosomes. We found that rno‐miR‐34c‐3p was downregulated in MSCs cocultured with ALI exosomes. MiR‐34c‐3p inhibitor promoted the proliferation and migration of MSCs. Moreover, the dual‐luciferase reporter assay demonstrated that miR‐34c‐3p regulated Janus kinase 1 (JAK1) expression. The miR‐34c‐3p inhibitor also significantly activated the JAK1/signal transducer and activator of transcription 3 (STAT3) signaling pathway. In conclusion, ALI exosomes decrease the miR‐34c‐3p expression levels, influencing MSCs via the JAK1/STAT3 signaling pathway.
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