Human 17β-hydroxysteroid dehydrogenase type 2 messenger ribonucleic acid expression and localization in term placenta and in endometrium during the menstrual cycle

被引:80
作者
Mustonen, MVJ
Isomaa, VV
Vaskivuo, T
Tapanainen, J
Poutanen, MH
Stenbäck, F
Vihko, RK
Vihko, PT
机构
[1] Univ Oulu, Dept Clin Chem, FIN-90220 Oulu, Finland
[2] Univ Oulu, Dept Obstet & Gynecol, FIN-90220 Oulu, Finland
[3] Univ Oulu, Dept Pathol, FIN-90220 Oulu, Finland
[4] Univ Oulu, Bioctr Oulu, WHO Collaborating Ctr Res Human Reprod, FIN-90220 Oulu, Finland
关键词
D O I
10.1210/jc.83.4.1319
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
According to the current hypothesis, 17 beta-hydroxysteroid dehydrogenases (17HSDs) regulate the extent of estrogen influence in the endometrium by converting estradiol (E-2) locally into a biologically less active sex steroid, estrone (E-1), and vice versa. Recently, we have shown that both 17HSD type 1 and type 2 are expressed in the human endometrium, and in the present work, using in situ hybridization, we show that 17HSD type 2 is localized in the glandular epithelial cells as previously shown for the type 1 enzyme, but in contrast to type 1, the expression of type 2 is highest at the end of the cycle. Hence, we hypothesize that the differential expression of the two 17HSD enzymes, with opposite activities in same cell types, could modulate intracellular E-2 concentrations during the end of the luteal phase of the menstrual cycle. We further analyzed the expression of 17HSD type 1 and type 2 mRNAs in term human placenta. Expression of 17HSD type 1 mRNA was detected in the syncytiotrophoblasts, and signals for type 2 mRNA were found inside the villi, corresponding to cytotrophoblasts. The expression of 17HSD type 2 in the placenta may serve to maintain the presence of inactive sex steroids and attenuate the formation of biologically potent androgens and estrogens.
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页码:1319 / 1324
页数:6
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