Suzuki H
Department of Orthopedic Surgery, Akita University School of Medicine, Japan.
Nihon Seikeigeka Gakkai Zasshi. 1994 Apr;68(4):172-83.
Fibronectin (FN) in the rheumatoid, and osteoarthritic, synovium was examined by light microscopy using immunostaining by fluorescein-labeled anti-fibronectin, or by peroxidase-labeled anti-fibronectin. Immunofluorescent FN was found more in the rheumatoid synovium than in the osteoarthritic synovium. The mean fluorescence intensity in a given area of the synovium including the synovial surface in rheumatoid arthritis was significantly higher than in osteoarthritis. As there was a significant correlation between the fluorescence intensity in the synovium and the number of synovial lining cells immunostained with peroxidase-labeled anti-fibronectin, the fluorescence intensity appeared to depend on the number of synovial lining cells containing FN. FN in the rheumatoid synovium and synovial fluid cells was examined by electron microscopy after immunoperoxidase staining. Immunoelectron microscopy of the rheumatoid synovium demonstrated FN on the surface of both type-A and type-B cells, the collagen fibers, and within the mitochondria, in the endoplasmic reticulum of type-B cells, and in the intercellular contact zone. These findings suggested that FN was mainly produced in the type-B cells, and played a role in maintaining the synovial structure. Immunoelectron microscopy of the rheumatoid synovial fluid cells confirmed the presence of FN on their surfaces. This suggested that FN opsonized by adhering debris to FN on the cell surfaces in the synovial fluid. The concentration of FN in the rheumatoid, and osteoarthritic, synovial fluids was measured by single radial immunodiffusion. The FN concentration in the rheumatoid synovial fluids was significantly higher than in the osteoarthritic synovial fluids. However, it was not significantly correlated with the indices of inflammatory activity such as with the C-reactive protein, the erythrocyte sedimentation rate, or catalase activity measured by a gasometry, or with the number of polymorphonucleated cells.
采用荧光素标记抗纤连蛋白或过氧化物酶标记抗纤连蛋白的免疫染色方法,通过光学显微镜对类风湿性关节炎和骨关节炎滑膜中的纤连蛋白(FN)进行检测。发现免疫荧光FN在类风湿性关节炎滑膜中比在骨关节炎滑膜中更多。类风湿性关节炎中包括滑膜表面在内的滑膜给定区域的平均荧光强度显著高于骨关节炎。由于滑膜中的荧光强度与用过氧化物酶标记抗纤连蛋白免疫染色的滑膜衬里细胞数量之间存在显著相关性,荧光强度似乎取决于含有FN的滑膜衬里细胞数量。对类风湿性关节炎滑膜和滑膜液细胞中的FN进行免疫过氧化物酶染色后,通过电子显微镜检查。类风湿性关节炎滑膜的免疫电子显微镜显示,A型和B型细胞表面、胶原纤维上、线粒体中、B型细胞内质网中以及细胞间接触区域均有FN。这些发现表明,FN主要在B型细胞中产生,并在维持滑膜结构中发挥作用。类风湿性关节炎滑膜液细胞的免疫电子显微镜证实其表面存在FN。这表明滑膜液中FN通过将碎片粘附在细胞表面的FN上而发挥调理作用。采用单向免疫扩散法测量类风湿性关节炎和骨关节炎滑膜液中FN的浓度。类风湿性关节炎滑膜液中FN浓度显著高于骨关节炎滑膜液。然而,它与炎症活动指标如C反应蛋白、红细胞沉降率、通过气体分析法测量的过氧化氢酶活性或多形核细胞数量均无显著相关性。