Yamamoto H, Murawaki Y, Kawasaki H
2nd Department of Internal Medicine, Tottori University School of Medicine, Yonago, Japan.
Res Commun Chem Pathol Pharmacol. 1992 Apr;76(1):95-112.
To clarify the role of individual collagenolytic cathepsin in hepatic collagen degradation, cathepsin B and L activities were determined in normal and CCl4-induced fibrotic liver, together with non-collagenolytic cathepsin H. Cathepsin B and L activities increased 1.9- and 2.0- fold, respectively, in the fibrotic liver as compared with the normal liver, and were significantly correlated with hepatic hydroxyproline levels. By contrast, cathepsin H activity was not altered in fibrotic rats. Similar results were also obtained from autopsied human livers. These results suggest that cathepsin B and L are similarly induced by hepatic collagen levels and are implicated in degrading collagens, especially soluble collagen.
为阐明单个胶原水解组织蛋白酶在肝脏胶原降解中的作用,我们测定了正常肝脏和四氯化碳诱导的纤维化肝脏中组织蛋白酶B和L的活性,以及非胶原水解组织蛋白酶H的活性。与正常肝脏相比,纤维化肝脏中组织蛋白酶B和L的活性分别增加了1.9倍和2.0倍,且与肝脏羟脯氨酸水平显著相关。相比之下,纤维化大鼠中组织蛋白酶H的活性没有改变。从尸检的人类肝脏中也得到了类似的结果。这些结果表明,组织蛋白酶B和L同样受肝脏胶原水平的诱导,并且参与胶原的降解,尤其是可溶性胶原的降解。