Regulation of cytochrome P450 cholesterol side-chain cleavage, 3 beta-hydroxysteroid dehydrogenase Delta 5-Delta 4 isomerase type 1 and estradiol 17 beta-hydroxysteroid dehydrogenase mRNA levels by calcium in human choriocarcinoma JEG-3 cells

被引:22
作者
Beaudoin, C
Bonenfant, M
Tremblay, Y
机构
[1] CHUL, RES CTR, CHUQ, MOL ENDOCRINOL LAB, QUEBEC CITY, PQ G1V 4G2, CANADA
[2] UNIV LAVAL, CTR HOSP, DEPT PHYSIOL, QUEBEC CITY, PQ G1V 4G2, CANADA
基金
加拿大自然科学与工程研究理事会;
关键词
placenta; steroidogenesis; gene regulation; P450scc; 3 beta-hydroxysteroid dehydrogenase type 1; 17 beta-hydroxysteroid dehydrogenase type 1; calcium; protein kinase A; protein kinase C;
D O I
10.1016/S0303-7207(97)00143-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In human placenta the cytochrome P450 side-chain cleavage (P450scc) and 3 beta-hydroxysteroid dehydrogenase type I (3 beta-HSD-1) convert cholesterol and pregnenolone producing progesterone, whereas 17 beta-hydroxysteroid dehydrogenase type 1 (17 beta-HSD-1) mediates the interconversion of estrone and estradiol. We have examined the effects of calcium on phorbol ester-and cAMP-induced P450scc, 3 beta-HSD-1 and 17 beta-HSD-1 mRNAs in human JEG-3 cells. A23187 increased in a dose-dependent fashion in the 1.3 kb 17 beta-HSD-1 mRNA whereas a weaker increase followed by a gradual depletion effect of A23187 was observed on 3 beta-HSD-1 mRNA. No significant effect of A23187 on P450scc mRNA was observed. Using 0.50 mu M of A23187 the induction of 3 beta-HSD-1 and 17 beta-HSD-1 mRNAs was maximum within about 6 h whereas P450scc mRNA levels stayed unaffected throughout the time-course period. The action of A23187 was synergistic on cAMP-stimulated 17 beta-HSD-1 mRNA levels, while in a dose-dependent manner A23187 progressively depleted 3 beta-HSD-1 and P450scc mRNA abundance probably by activation of a calcium-/calmodulin-dependent phosphodiesterase. On the phorbol 12-myristate, 13-acetate (PMA)-stimulated 3 beta-HSD-1, 17 beta-HSD-1 and P450scc mRNA levers only the lowest concentration of A23187 potentialized the PMA effect on the I7 beta-HSD-1 mRNA levels. Using thapsigargin (TG), a cell-permeable sesquiterpene lactone that releases calcium by inhibiting sarco/endoplasmic reticular calcium-ATPase, our data indicated the presence in JEG-3 cells of TG-sensitive and TG-insensitive calcium-ATPases regulating 3 beta-HSD-1 and 17 beta-HSD-1 mRNA levels. These results emphasized the complexity of calcium contribution with the protein kinase A and C pathways in the regulation of P450scc, 3 beta-HSD-1 and 17 beta-HSD-1 mRNA levels. In addition, the different sensitivity of these genes to calcium suggest they could be activated by different subclasses of PKCs. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:63 / 71
页数:9
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