Gaertner U
Z Gastroenterol. 1978 Apr;16(4):251-6.
The regulation of hepatic cholesterol biosynthesis by low density lipoprotein (LDL) was studied by using a new cell culture method of isolated rat hepatocytes. After two days in culture no supressant effect of LDL on 3-hydroxy-3-methylglutaryl coenzyme A reductase activity (HMG-CoA) was detected. The primary culture of rat hepatocytes lead to the growth of a cell monolayer with stable liver specific properties during 4 days of culture. LDL did suppress HMG-CoA-reductase activity of rat hepatocytes in primary culture 5 days after seeding, when dedifferentiation has started.
采用分离的大鼠肝细胞新细胞培养方法,研究了低密度脂蛋白(LDL)对肝脏胆固醇生物合成的调节作用。培养两天后,未检测到LDL对3-羟基-3-甲基戊二酰辅酶A还原酶活性(HMG-CoA)有抑制作用。大鼠肝细胞原代培养在4天培养期间形成具有稳定肝脏特异性性质的细胞单层。接种5天后,当去分化开始时,LDL确实抑制了原代培养大鼠肝细胞的HMG-CoA还原酶活性。