Chondrocytes play a role in the development of rheumatoid arthritis via TMEM147-mediated NF-κB activation.

ARTHRITIS & RHEUMATOLOGY(2020)

引用 25|浏览22
暂无评分
摘要
Objective We have previously reported that the coactivation of NF-kappa B and STAT3 in nonimmune cells, including synovial fibroblasts, enhances the expression of NF-kappa B target genes and plays a role in chronic inflammation and rheumatoid arthritis (RA). This study was undertaken to examine the role of NF-kappa B activation in chondrocytes and better understand the pathogenesis of RA. Furthermore, transmembrane protein 147 (TMEM147) was investigated as a representative NF-kappa B activator in chondrocytes. Methods Clinical samples from RA patients were analyzed by immunohistochemistry. Specimens obtained from patients with polydactyly were used as control samples. The functional contribution of chondrocytes and TMEM147 to arthritis was examined in several murine models of RA. In vitro experiments (quantitative polymerase chain reaction, RNA interference, immunoprecipitation, and confocal microscopy) were performed to investigate the mechanism of action of TMEM147 in chondrocytes. Results Samples obtained from RA patients and mouse models of RA showed coactivation of NF-kappa B and STAT3 in chondrocytes (P < 0.001). This coactivation induced a synergistic expression of NF-kappa B targets in vitro (P < 0.01). Chondrocyte-specific deletion of STAT3 significantly suppressed the development of cytokine-induced RA (P < 0.01). TMEM147 was highly expressed in chondrocytes from RA patient samples and the mouse models of RA. Gene silencing of TMEM147 or anti-TMEM147 antibody treatment inhibited the cytokine-mediated activation of NF-kappa B in vitro (P < 0.01) and suppressed cytokine-induced RA in vivo (P < 0.01). Mechanistically, TMEM147 molecules acted as scaffold proteins for the NF-kappa B complex, which included breakpoint cluster region and casein kinase 2, and enhanced NF-kappa B activity. Conclusion These results suggest that chondrocytes play a role in the development of RA via TMEM147-mediated NF-kappa B activation and indicate a novel therapeutic strategy for RA.
更多
查看译文
关键词
Chondrocytes,Cytokines,Inflammation,NF-κB,Rheumatoid arthritis,TMEM147
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要