Hansen T, Petrow P K, Gaumann A, Keyszer G, Bräuer R, Kriegsmann J
Johannes Gutenberg University Mainz, Institute for Pathology, Germany.
Exp Toxicol Pathol. 2000 Aug;52(4):312-6. doi: 10.1016/S0940-2993(00)80055-X.
This study was designed to investigate the expression of the matrix degrading proteinase cathepsin B and its endogenous inhibitor cystatin C in rheumatoid arthritis (RA) with special regard to multinucleated synovial giant cells (SGC). We applied an immunohistochemical double-labeling technique. SGC strongly expressed cystatin C and CD68, but were negative for cathepsin B. This staining pattern occurred in osteoclasts as well. Our findings support the idea that in RA matrix destruction by cathepsin B is not mediated by SGC or osteoclasts, but by mononuclear synoviocytes.
本研究旨在探讨基质降解蛋白酶组织蛋白酶B及其内源性抑制剂胱抑素C在类风湿关节炎(RA)中的表达,特别关注多核滑膜巨细胞(SGC)。我们应用了免疫组织化学双重标记技术。SGC强烈表达胱抑素C和CD68,但组织蛋白酶B呈阴性。这种染色模式在破骨细胞中也存在。我们的研究结果支持以下观点:在RA中,组织蛋白酶B介导的基质破坏不是由SGC或破骨细胞介导的,而是由单核滑膜细胞介导的。