Melnykovych G, Clowes K K
Biochim Biophys Acta. 1983 Mar 31;756(2):138-43. doi: 10.1016/0304-4165(83)90084-3.
Cell line C-4-1 which produces alkaline phosphatase (EC 3.1.1.4) of the placental type in response to glucocorticoids was grown in the presence of inhibitors of mevalonate formation for periods ranging from 1 to 4 days. When C-4-1 cells were incubated in the presence of 25-hydroxycholesterol (1 microM) or compactin (11.6 microM) the induction of alkaline phosphatase by 0.2 microM dexamethasone was suppressed. This suppression could be partially prevented by the addition of mevalonolactone to the growing culture. The reversal effect by mevalonate was most evident with compactin, a well known competitive inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A reductase. In contrast, the effect of tunicamycin which inhibits N-linked protein glycosylation and also prevents alkaline phosphatase induction by glucocorticoids could not be reversed by mevalonate. These results implicate mevalonate in alkaline phosphatase induction, possibly through its role as a precursor of dolichols.
能响应糖皮质激素产生胎盘型碱性磷酸酶(EC 3.1.1.4)的C - 4 - 1细胞系,在甲羟戊酸形成抑制剂存在的情况下培养1至4天。当C - 4 - 1细胞在25 - 羟基胆固醇(1微摩尔)或洛伐他汀(11.6微摩尔)存在的情况下孵育时,0.2微摩尔地塞米松对碱性磷酸酶的诱导作用受到抑制。向正在生长的培养物中添加甲羟戊酸内酯可以部分阻止这种抑制作用。甲羟戊酸的逆转作用在洛伐他汀(一种著名的3 - 羟基 - 3 - 甲基戊二酰辅酶A还原酶竞争性抑制剂)存在时最为明显。相比之下,抑制N - 连接蛋白糖基化且也能阻止糖皮质激素诱导碱性磷酸酶的衣霉素的作用不能被甲羟戊酸逆转。这些结果表明甲羟戊酸参与碱性磷酸酶的诱导,可能是通过其作为多萜醇前体的作用。