Takahashi S, Koda K
Biochem J. 1984 May 15;220(1):157-64. doi: 10.1042/bj2200157.
We have postulated that an insufficient active of collagenase relative to increased collagen synthesis may be the cause of the increased collagen accumulation in fibrotic tissues. In the present study, 125I-collagenase and rabbit anti-collagenase immunoglobulin G were used to develop a sensitive radioimmunoassay that detects 0.1 nM (3 ng) of collagenase protein in tissue samples. The assay also can detect collagenase protein that is associated with extracellular-matrix collagen fibrils. Good correlation with an assay of enzyme activity validates the radioimmunoassay for quantification of collagenase. The assay was used to measure amounts of collagenase in relation to fibrotic processes in livers of mice with schistosomiasis. Results indicate that the amounts of collagenase relative to synthesized collagens were significantly lower, and this may contribute to the progressive fibrosis. The occurrence of a maximum amount of collagenase at 7 weeks after infection with Schistosoma mansoni cercariae in concanavalin A-treated animals, as compared with 8 weeks in controls, could account for the large remission of fibrosis in mice so treated. The results emphasize the possible importance of collagenase in controlling or limiting fibrosis.
我们推测,相对于胶原蛋白合成增加,胶原酶活性不足可能是纤维化组织中胶原蛋白积累增加的原因。在本研究中,使用125I-胶原酶和兔抗胶原酶免疫球蛋白G开发了一种灵敏的放射免疫测定法,该方法可检测组织样本中0.1 nM(3 ng)的胶原酶蛋白。该测定法还可以检测与细胞外基质胶原纤维相关的胶原酶蛋白。与酶活性测定的良好相关性验证了用于定量胶原酶的放射免疫测定法。该测定法用于测量血吸虫病小鼠肝脏中与纤维化过程相关的胶原酶量。结果表明,相对于合成的胶原蛋白,胶原酶的量显著降低,这可能导致进行性纤维化。与对照组8周相比,在伴刀豆球蛋白A处理的动物中,感染曼氏血吸虫尾蚴7周时胶原酶出现最大量,这可以解释经如此处理的小鼠纤维化的大量缓解。结果强调了胶原酶在控制或限制纤维化方面可能的重要性。