Taylor F R, Kandutsch A A
Jackson Laboratory, Bar Harbor, ME 04609.
J Lipid Res. 1989 Jun;30(6):899-905.
Three mammalian cell lines were examined for their ability to metabolize the regulatory oxysterol, 25-hydroxycholesterol, and derepress 3-hydroxy-3-methylglutaryl CoA reductase. In mouse L cell fibroblasts reductase activity was restored with the concomitant metabolism of 25-hydroxycholesterol via side-chain hydroxylation and scission of the C20-C22 bond. Chinese hamster lung cells did not appear to derepress the reductase and these cells and Chinese hamster ovary cells did not metabolize 25-hydroxycholesterol to a significant extent. Only 5-10% of the oxysterol became esterified with a fatty acid in any of the cell lines when grown in the described culture conditions.
检测了三种哺乳动物细胞系代谢调节性氧化甾醇25-羟基胆固醇以及解除3-羟基-3-甲基戊二酰辅酶A还原酶抑制的能力。在小鼠L细胞成纤维细胞中,25-羟基胆固醇通过侧链羟基化和C20-C22键断裂进行代谢,同时还原酶活性得以恢复。中国仓鼠肺细胞似乎并未解除还原酶的抑制,并且这些细胞以及中国仓鼠卵巢细胞在很大程度上并未代谢25-羟基胆固醇。在所描述的培养条件下生长时,在任何细胞系中,只有5%-10%的氧化甾醇与脂肪酸酯化。