Tanuma S, Kawashima K, Endo H
Department of Physiological Chemistry, Faculty of Pharmaceutical Sciences, Teikyo University, Kanagawa, Japan.
Biochim Biophys Acta. 1987 Nov 20;910(2):197-201. doi: 10.1016/0167-4781(87)90073-x.
The induction capacity of dexamethasone, a synthetic glucocorticoid, for the synthesis of metallothionein was about the same as that of 3-aminobenzamide, which is an inhibitor of ADP-ribosylation of chromosomal proteins, in cultured mouse mammary tumor cells. Both inductions of metallothionein were temporally correlated with a decrease in the amount of endogenous poly (ADP-ribose) on nonhistone high-mobility-group 14 and 17 proteins. In contrast, the extent of cadmium-induced metallothionein synthesis was 2-3-times that of dexamethasone or 3-aminobenzamide. However, cadmium had essentially no effect on de-ADP-ribosylation of these proteins.
在培养的小鼠乳腺肿瘤细胞中,合成糖皮质激素地塞米松诱导金属硫蛋白合成的能力与3-氨基苯甲酰胺(一种染色体蛋白ADP-核糖基化抑制剂)的诱导能力大致相同。金属硫蛋白的这两种诱导均与非组蛋白高迁移率族14和17蛋白上内源性聚(ADP-核糖)量的减少在时间上相关。相比之下,镉诱导的金属硫蛋白合成程度是地塞米松或3-氨基苯甲酰胺的2至3倍。然而,镉对这些蛋白的去ADP-核糖基化基本没有影响。