促炎细胞因子
微泡
间充质干细胞
细胞凋亡
细胞生物学
生物
软骨细胞
脂多糖
NF-κB
小RNA
癌症研究
肿瘤坏死因子α
骨髓
炎症
信号转导
免疫学
软骨
解剖
生物化学
基因
作者
Lei He,Yuyong Chen,Zekai Ke,Mao Pang,Baofeng Yang,Feng Feng,Zizhao Wu,Chang Liu,Bin Liu,Xiaozuo Zheng,Tao Wu,Tao Shu
出处
期刊:Gene
[Elsevier]
日期:2020-08-01
卷期号:751: 144764-144764
被引量:29
标识
DOI:10.1016/j.gene.2020.144764
摘要
Bone marrow mesenchymal stem cells (BMSCs)-derived exosomes (Exos) have anti-inflammatory and anti-apoptotic functions. miRNA-210 has also been confirmed to play a role in inhibiting proinflammatory cytokines. Herein, we aimed to explore the effects of Exos derived from miRNA-210-overexpressing BMSCs (BMSCs-210-Exos) and the mechanisms by which they provide protection to chondrocytes from lipopolysaccharide (LPS)-induced injury. BMSCs were transfected with or without miRNA-210. Exos substantially improved the proliferation of chondrocytes and inhibited LPS-induced cell apoptosis. Furthermore, BMSCs-210-Exos promoted the proliferation of chondrocytes and prevented LPS-induced cell apoptosis better than BMSCs-Exos not overexpressing miRNA-210. In addition, tumor necrosis factor receptor superfamily member 21 (Tnfrsf21) expression was inhibited and the NF-κB pathway was attenuated by both BMSCs-Exos and BMSCs-210-Exos during LPS-induced chondrocyte injury. Collectively, these results suggest that BMSCs-210-Exos enhance the protection of chondrocytes from LPS-induced injury via the NF-κB pathway.
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