Bartlomowicz B, Waxman D J, Utesch D, Oesch F, Friedberg T
Institute of Toxicology, University of Mainz, FRG.
Carcinogenesis. 1989 Jan;10(1):225-8. doi: 10.1093/carcin/10.1.225.
We present data showing that the major phenobarbital inducible cytochromes P-450 (cytochrome P-450IIB1 and cytochrome P-450IIB2) were phosphorylated in intact hepatocytes. This phosphorylation was greatly increased by the cAMP derivatives N6-dibutyryl-cAMP and 8-thiomethyl-cAMP mediated by a cAMP-dependent protein kinase. Most importantly the phosphorylation status of cytochromes P-450 was shown to change in the hepatocytes after treatment with glucagon, which is known to increase the level of cAMP in hepatocytes. The observed impact of the hormone glucagon on the phosphorylation of distinct cytochrome P-450 forms in intact hepatocytes reveals the possibility that the enzyme activity of cytochromes P-450 could be rapidly and differentially regulated by their phosphorylation and therefore dependent on the hormonal status of the organism.
我们提供的数据表明,主要的苯巴比妥诱导型细胞色素P-450(细胞色素P-450IIB1和细胞色素P-450IIB2)在完整的肝细胞中发生了磷酸化。环磷酸腺苷(cAMP)衍生物N6-二丁酰-cAMP和8-硫代甲基-cAMP通过cAMP依赖性蛋白激酶介导,使这种磷酸化作用大大增强。最重要的是,在用胰高血糖素处理肝细胞后,细胞色素P-450的磷酸化状态发生了变化,已知胰高血糖素会增加肝细胞中cAMP的水平。观察到的激素胰高血糖素对完整肝细胞中不同细胞色素P-450形式磷酸化的影响揭示了一种可能性,即细胞色素P-450的酶活性可能通过其磷酸化作用而被快速且差异地调节,因此依赖于生物体的激素状态。