Krumbholz Grit, Junker Susann, Meier Florian M P, Rickert Markus, Steinmeyer Jürgen, Rehart Stefan, Lange Uwe, Frommer Klaus W, Schett Georg, Müller-Ladner Ulf, Neumann Elena
Department of Internal Medicine and Rheumatology, Justus-Liebig-University, Giessen, and Kerckhoff-Klinik, Bad Nauheim, Germany.
Department of Orthopaedics and Orthopaedic Surgery, University Hospital Giessen and Marburg, Giessen, Germany.
Clin Exp Rheumatol. 2017 May-Jun;35(3):406-414. Epub 2017 Jan 5.
Adiponectin is an effector molecule in the pathophysiology of rheumatoid arthritis, e.g. by inducing cytokines and matrix degrading enzymes in synovial fibroblasts. There is growing evidence that adiponectin affects osteoblasts and osteoclasts although the contribution to the aberrant bone metabolism in rheumatoid arthritis is unclear. Therefore, the adiponectin effects on rheumatoid arthritis-derived osteoblasts and osteoclasts were evaluated.
Adiponectin and its receptors were examined in bone tissue. Primary human osteoblasts and osteoclasts were stimulated with adiponectin and analysed using realtime polymerase chain-reaction and immunoassays. Effects on matrix-production by osteoblasts and differentiation and resorptive activity of osteoclasts were examined.
Immunohistochemistry of rheumatoid arthritis bone tissue showed adiponectin expression in key cells of bone remodelling. Adiponectin altered gene expression and cytokine release in osteoblasts and increased IL-8 secretion by osteoclasts. Adiponectin inhibited osterix and induced osteoprotegerin mRNA in osteoblasts. In osteoclasts, MMP-9 and tartrate resistant acid phosphatase expression was increased. Accordingly, mineralisation capacity of osteoblasts decreased whereas resorptive activity of osteoclasts increased.
The results confirm the proinflammatory potential of adiponectin and support the idea that adiponectin influences rheumatoid arthritis bone remodelling through alterations in osteoblast and osteoclast.
脂联素是类风湿关节炎病理生理学中的一种效应分子,例如通过诱导滑膜成纤维细胞中的细胞因子和基质降解酶发挥作用。越来越多的证据表明脂联素会影响成骨细胞和破骨细胞,尽管其在类风湿关节炎异常骨代谢中的作用尚不清楚。因此,对脂联素对类风湿关节炎来源的成骨细胞和破骨细胞的作用进行了评估。
检测骨组织中的脂联素及其受体。用脂联素刺激原代人成骨细胞和破骨细胞,并使用实时聚合酶链反应和免疫测定法进行分析。检测对成骨细胞基质产生、破骨细胞分化和吸收活性的影响。
类风湿关节炎骨组织的免疫组织化学显示脂联素在骨重塑的关键细胞中表达。脂联素改变了成骨细胞中的基因表达和细胞因子释放,并增加了破骨细胞的白细胞介素-8分泌。脂联素抑制成骨细胞中的osterix并诱导骨保护素mRNA表达。在破骨细胞中,基质金属蛋白酶-9和抗酒石酸酸性磷酸酶表达增加。相应地,成骨细胞的矿化能力下降,而破骨细胞的吸收活性增加。
结果证实了脂联素的促炎潜力,并支持脂联素通过改变成骨细胞和破骨细胞影响类风湿关节炎骨重塑的观点。