| Literature DB >> 33414452 |
Qiang Guo1,2,3, Ximiao Chen1,2,4, Jiaoxiang Chen1,2,3, Gang Zheng1,2,3, Chenglong Xie1,2,3, Hongqiang Wu1,2,3, Zhimin Miao1,2,3, Yan Lin1,2,3, Xiangyang Wang1,2,3, Weiyang Gao1,2,3, Xiangtao Zheng5, Zongyou Pan6, Yifei Zhou7,8,9, Yaosen Wu10,11,12, Xiaolei Zhang13,14,15,16.
Abstract
Damaged deoxyribonucleic acid (DNA) is a primary pathologic factor for osteoarthritis (OA); however, the mechanism by which DNA damage drives OA is unclear. Previous research demonstrated that the cyclic GMP-AMP synthase (cGAS)-stimulator of interferon genes (STING) participates in DNA damage response. As a result, the current study aimed at exploring the role STING, which is the major effector in the cGAS-STING signaling casacde, in OA progress in vitro, as well as in vivo. In this study, the expression of STING was evaluated in the human and mouse OA tissues, and in chondrocytes exposed to interleukin-1 beta (IL-1β). The influences of STING on the metabolism of the extracellular matrix (ECM), apoptosis, and senescence, were assessed in STING overexpressing and knocking-down chondrocytes. Moreover, the NF-κB-signaling casacde and its role in the regulatory effects of STING on ECM metabolism, apoptosis, and senescence were explored. The STING knockdown lentivirus was intra-articularly injected to evaluate its therapeutic impact on OA in mice in vivo. The results showed that the expression of STING was remarkably elevated in the human and mouse OA tissues and in chondrocytes exposed to IL-1β. Overexpression of STING promoted the expression of MMP13, as well as ADAMTS5, but suppressed the expression of Aggrecan, as well as Collagen II; it also enhanced apoptosis and senescence in chondrocytes exposed to and those untreated with IL-1β. The mechanistic study showed that STING activated NF-κB signaling cascade, whereas the blockage of NF-κB signaling attenuated STING-induced apoptosis and senescence, and ameliorated STING-induced ECM metabolism imbalance. In in vivo study, it was demonstrated that STING knockdown alleviated destabilization of the medial meniscus-induced OA development in mice. In conclusion, STING promotes OA by activating the NF-κB signaling cascade, whereas suppression of STING may provide a novel approach for OA therapy.Entities:
Year: 2021 PMID: 33414452 PMCID: PMC7791051 DOI: 10.1038/s41419-020-03341-9
Source DB: PubMed Journal: Cell Death Dis Impact factor: 8.469