Zou Renling, Huang Xiayang, Xu Peng
College of Medical Instrument and Food Engineering, University of Shanghai for Science and Technology, Shanghai, China.
The University of British Columbia, Vancouver, Canada.
Biochem Biophys Rep. 2021 Feb 6;26:100934. doi: 10.1016/j.bbrep.2021.100934. eCollection 2021 Jul.
Rheumatoid arthritis (RA) is a chronic immune disease characterized by synovitis and bone destruction. The osteoclasts play a critical role in pathologic bone loss during inflammatory arthritis. In this paper, we report that Interleukin (IL)-6, IL-6Rα/gp130, IL-11, IL-27, and Matrix Metallo Proteinases (MMP)-9 expression results in serum of the RA group were significantly higher than that of the control group. The gp130 positive cells in peripheral blood mononuclear cell (PBMC) and osteoclast-like cells (OLC) which had been induced with receptor activator of nuclear factor κB ligand (RANKL) in RA group were also higher than that in the control group. In addition, after OLC in RA group is cultured with -gp130 Monoclonal antibody (McAb), the IL-6 and MMP-9 expression in osteoclast supernatant insignificantly decreased. Meanwhile, the expression results of Tartrate Resistant Acid Phosphatase (TRAP)-positive cells and osteoclasts were also decreased significantly. Our study suggests that regulating gp130 receptor can be used to control the differentiation and formation of osteoclasts, which provides a new clinical strategy for RA patients in the future.
类风湿性关节炎(RA)是一种以滑膜炎和骨质破坏为特征的慢性免疫疾病。破骨细胞在炎症性关节炎的病理性骨质流失中起关键作用。在本文中,我们报道RA组血清中白细胞介素(IL)-6、IL-6Rα/gp130、IL-11、IL-27和基质金属蛋白酶(MMP)-9的表达结果显著高于对照组。RA组经核因子κB受体激活剂(RANKL)诱导的外周血单核细胞(PBMC)和破骨细胞样细胞(OLC)中的gp130阳性细胞也高于对照组。此外,RA组的OLC用-gp130单克隆抗体(McAb)培养后,破骨细胞上清液中IL-6和MMP-9的表达无明显下降。同时,抗酒石酸酸性磷酸酶(TRAP)阳性细胞和破骨细胞的表达结果也显著下降。我们的研究表明,调节gp130受体可用于控制破骨细胞的分化和形成,这为未来RA患者提供了一种新的临床策略。