Hadler N M, Spitznagel J K, Quinet R J
J Immunol. 1979 Aug;123(2):572-7.
The concentrations of several polymorphonuclear neutrophilic lysosomal constituents were quantitated by immunochemical and enzymatic assays in 28 inflammatory and 9 noninflammatory synovial fluids. The quantities of lactoferrin, myeloperoxidase, and enzymatically determined lysozyme were covariate with the neutrophil count. Enzymatic activities measured with synthetic substrates developed for the assay of chymotryptic-like cationic protein (cathepsin G) and elastase, along with immunochemically determined lysozyme, were independent of the neutrophil count. Although the latter assays were developed and standardized with human neutrophilic lysosomal constituents, they measure different activities in inflammatory synovial effusions. No elastase was detected if elastin was used as the substrate. Regardless of the source of the enzymes, there was a negative correlation between their concentration and the degree of radiographic destruction of the joint from which the fluid was obtained. Lysosomal enzymes in solution in synovial fluid are not likely to be primarily involved in cartilage destruction.
通过免疫化学和酶法检测,对28份炎性和9份非炎性滑液中几种多形核中性粒细胞溶酶体成分的浓度进行了定量分析。乳铁蛋白、髓过氧化物酶和酶法测定的溶菌酶含量与中性粒细胞计数相关。用为检测类胰凝乳蛋白酶样阳离子蛋白(组织蛋白酶G)和弹性蛋白酶而开发的合成底物测定的酶活性,以及免疫化学测定的溶菌酶,与中性粒细胞计数无关。尽管后一种检测方法是用人中性粒细胞溶酶体成分开发并标准化的,但它们在炎性滑液中测量的是不同的活性。如果使用弹性蛋白作为底物,则未检测到弹性蛋白酶。无论酶的来源如何,其浓度与获取滑液的关节的放射学破坏程度之间均呈负相关。滑液中溶液状态的溶酶体酶不太可能是软骨破坏的主要原因。