| Literature DB >> 32428694 |
Lei He1, Yuyong Chen1, Zekai Ke2, Mao Pang1, Bu Yang1, Feng Feng1, Zizhao Wu1, Chang Liu1, Bin Liu1, Xiaozuo Zheng3, Tao Wu4, Tao Shu5.
Abstract
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.Entities:
Keywords: Bone mesenchymal stem cells; Chondrocytes; Exosomes; NF-κB; miRNA-210
Year: 2020 PMID: 32428694 DOI: 10.1016/j.gene.2020.144764
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688