Dahl I M, Husby G
Ann Rheum Dis. 1985 Oct;44(10):647-57. doi: 10.1136/ard.44.10.647.
Organ cultures and primary cell cultures were established from synovial tissue collected from patients with rheumatoid arthritis. Hyaluronic acid measured by the incorporation of [3H]glucosamine into the polysaccharide was found to be synthesised in the cultures immediately after transfer from in-vivo to in-vitro conditions. This was in contrast to the primary cultures established from cells isolated from normal joints. The latter cells did not synthesise any detectable hyaluronate. 90-100% of the cells in primary culture were found to be esterase positive, indicating their macrophage nature. The molecular weight of the hyaluronate produced by the pathological cells was low (approximately 50 000) compared with the molecular weight of hyaluronate found in joint fluid from normal or rheumatoid joints. Cell lines of fibroblasts established from rheumatoid joints and studied after four or seven passages also produced hyaluronate of low molecular weight. It is known that similar cell lines from normal joints produce a high molecular weight polymer.
从类风湿性关节炎患者的滑膜组织中建立了器官培养物和原代细胞培养物。通过将[3H]葡萄糖胺掺入多糖中来测量透明质酸,发现其在从体内转移到体外条件后立即在培养物中合成。这与从正常关节分离的细胞建立的原代培养物形成对比。后一种细胞不合成任何可检测到的透明质酸盐。发现原代培养物中90-100%的细胞酯酶呈阳性,表明它们具有巨噬细胞性质。与正常或类风湿性关节的关节液中发现的透明质酸分子量相比,病理细胞产生的透明质酸分子量较低(约50000)。从类风湿性关节建立并在传代四次或七次后进行研究的成纤维细胞系也产生低分子量的透明质酸。已知来自正常关节的类似细胞系产生高分子量聚合物。