Berteloot A, Chabot J G, Hugon J S
Biochim Biophys Acta. 1981 Dec 18;678(3):423-36. doi: 10.1016/0304-4165(81)90124-0.
The turnover of mouse intestinal brush border membrane enzymes has been studied by kinetic analysis of the evolution of enzyme activities during organ culture. By comparing the results obtained in these studies with the predictions from a mathematical model of enzyme synthesis and degradation in organ cultures, it has been possible to reach the following conclusions: (1) There is no degradation of brush border membrane enzymes during culture and the rate of synthesis of each enzyme is directly measurable from the kinetics of total enzyme accumulation (tissue + media). (2) Brush border membrane enzymes are released in culture media by two complementary processes. The first one involves a differential solubilization of enzymes but its exact nature cannot be exactly stated. The second one involves a microvesiculation of brush border membranes, the importance of which in vivo is seen in the possible conciliation between urinary membrane synthesis and heterogeneous turnover of membrane components.
通过对器官培养过程中酶活性演变进行动力学分析,研究了小鼠肠道刷状缘膜酶的周转情况。将这些研究结果与器官培养中酶合成和降解数学模型的预测结果进行比较,得出了以下结论:(1)培养过程中刷状缘膜酶没有降解,每种酶的合成速率可直接从总酶积累(组织+培养基)的动力学中测量得出。(2)刷状缘膜酶通过两个互补过程释放到培养基中。第一个过程涉及酶的差异溶解,但其确切性质尚不能明确阐述。第二个过程涉及刷状缘膜的微囊化,其在体内的重要性体现在尿膜合成与膜成分异质周转之间可能的协调上。