Williams R J, Smith R L, Schurman D J
Orthopedic Research Laboratory, Stanford University School of Medicine, California.
J Orthop Res. 1991 Mar;9(2):258-65. doi: 10.1002/jor.1100090214.
Human articular cartilage released significantly increased levels of metal-dependent enzymes capable of degrading collagen, casein, and gelatin at a neutral pH following exposure to a sterile, purified fraction of Staphylococcus aureus culture medium. Neutral metalloprotease activity was determined by radiolabeled substrate assays and substrate gel analysis. The enzymes were activated with 4-aminophenylmercuric acetate and were inhibited by 1,10-phenanthroline and ethylenediamine tetraacetic acid. Protein immunoblots demonstrated that type I collagenase and stromelysin (matrix metalloproteinase III) secretion was increased following staphylococcal medium challenge. The profile of enzymatic activity induced by staphylococcal medium was directly comparable to that observed with interleukin-1, which was used as a positive control. The staphylococcal medium had no inherent proteolytic activity. Increased production of the neutral metalloproteases collagenase and stromelysin may significantly contribute to the extensive cartilage destruction noted in staphylococcal septic arthritis.
在暴露于无菌、纯化的金黄色葡萄球菌培养基组分后,人类关节软骨释放出显著增加的金属依赖性酶水平,这些酶在中性pH值下能够降解胶原蛋白、酪蛋白和明胶。通过放射性标记底物测定和底物凝胶分析来确定中性金属蛋白酶活性。这些酶用乙酸4-氨基苯汞激活,并被1,10-菲咯啉和乙二胺四乙酸抑制。蛋白质免疫印迹表明,在金黄色葡萄球菌培养基刺激后,I型胶原酶和基质溶解素(基质金属蛋白酶III)的分泌增加。金黄色葡萄球菌培养基诱导的酶活性谱与用作阳性对照的白细胞介素-1所观察到的直接可比。金黄色葡萄球菌培养基没有内在的蛋白水解活性。中性金属蛋白酶胶原酶和基质溶解素产量的增加可能显著促成了在金黄色葡萄球菌败血症性关节炎中所观察到的广泛软骨破坏。