Jacob Shiju, Sudhakaran P R
Department of Biochemistry, University of Kerala, Kariavattom, Thiruvananthapuram 695 581, India.
Indian J Biochem Biophys. 2003 Oct;40(5):324-9.
Molecular mechanisms involved in mediating alteration in cell matrix interaction have been examined by studying the changes in the activity of matrix metalloproteinases (MMPs) in CCl4-induced regenerating liver, using zymography and ELISA. Activity of MMPs (72 kD, 92 kD and 130 kD gelatinases) in the rat liver increased progressively during acute injury till the 4th day and then decreased to near normal level after CCl4 administration (0.5 ml/100 g body wt.) on the 6th day. Hepatocyte lysate of injured liver on the 4th day showed significantly higher levels of MMP2 and MMP9 compared to the control. In the culture medium of hepatocytes, the levels of MMP2 and MMP9 increased progressively with the duration of culture, indicating that hepatocytes are the major source of these MMPs in regenerating liver. These results suggest an involvement of MMPs in matrix degradation and remodeling during regeneration after acute liver injury induced by CCl4.
通过酶谱分析和酶联免疫吸附测定法,研究四氯化碳诱导的再生肝中基质金属蛋白酶(MMPs)活性的变化,以此来探究介导细胞与基质相互作用改变的分子机制。在急性损伤期间,大鼠肝脏中MMPs(72 kD、92 kD和130 kD明胶酶)的活性逐渐升高,直至第4天,随后在第6天给予四氯化碳(0.5 ml/100 g体重)后降至接近正常水平。与对照组相比,第4天损伤肝脏的肝细胞裂解液中MMP2和MMP9的水平显著更高。在肝细胞培养基中,MMP2和MMP9的水平随着培养时间的延长而逐渐升高,这表明肝细胞是再生肝中这些MMPs的主要来源。这些结果表明,MMPs参与了四氯化碳诱导的急性肝损伤后再生过程中的基质降解和重塑。