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
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机构:CHUL, RES CTR, CHUQ, MOL ENDOCRINOL LAB, QUEBEC CITY, PQ G1V 4G2, CANADA
Beaudoin, C
Bonenfant, M
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h-index: 0
机构:CHUL, RES CTR, CHUQ, MOL ENDOCRINOL LAB, QUEBEC CITY, PQ G1V 4G2, CANADA
Bonenfant, M
Tremblay, Y
论文数: 0引用数: 0
h-index: 0
机构:CHUL, RES CTR, CHUQ, MOL ENDOCRINOL LAB, QUEBEC CITY, PQ G1V 4G2, CANADA
Tremblay, Y
机构:
[1] CHUL, RES CTR, CHUQ, MOL ENDOCRINOL LAB, QUEBEC CITY, PQ G1V 4G2, CANADA
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.