11Beta-hydroxysteroid dehydrogenase expression in first trimester human trophoblasts

Mol Cell Endocrinol. 1998 Jun 25;141(1-2):13-20. doi: 10.1016/s0303-7207(98)00103-8.

Abstract

This study evaluated the levels and the enzymatic characteristics of 11beta-hydroxysteroid dehydrogenase activity (11beta-HSD) of chorionic villi isolated from first trimester human placenta. The results demonstrated a predominant expression of the NAD-dependent dehydrogenase isoform (11beta-HSD2) over the NADP-dependent oxoreductase (11beta-HSD1). Thus, in tissue homogenates exogenous NAD increased the conversion of corticosterone to 11-dehydrocorticosterone of about 14-fold while NADP was ineffective. There was no conversion of 11-dehydrocorticosterone to corticosterone either with NADH or NADPH demonstrating the lack of reductase activity. In keeping with these results, RT-PCR analysis indicated a mRNA for 11beta-HSD2 in villous tissue while 11beta-HSD1 mRNA levels were undetectable. In addition, immunohistochemical staining localized the 11beta-HSD2 protein to syncytiotrophoblasts and cell columns of the chorionic villi. These results suggest roles for the trophoblast-associated 11beta-HSD2 oxidative activity in modulating the exposure of the embryo to active glucocorticoids in the early gestation and in regulating trophoblasts invasion of the uterine wall.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 11-beta-Hydroxysteroid Dehydrogenases
  • Blotting, Western
  • Chorionic Villi / enzymology
  • Corticosterone / metabolism
  • Female
  • Humans
  • Hydroxysteroid Dehydrogenases / analysis
  • Hydroxysteroid Dehydrogenases / genetics*
  • Hydroxysteroid Dehydrogenases / metabolism*
  • Immunohistochemistry
  • Isoenzymes / analysis
  • Isoenzymes / genetics
  • Isoenzymes / metabolism
  • NAD / metabolism
  • NADP / metabolism
  • Organ Specificity
  • Pregnancy
  • Pregnancy Trimester, First
  • RNA, Messenger / analysis
  • RNA, Messenger / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Trophoblasts / enzymology*

Substances

  • Isoenzymes
  • RNA, Messenger
  • NAD
  • NADP
  • Hydroxysteroid Dehydrogenases
  • 11-beta-Hydroxysteroid Dehydrogenases
  • Corticosterone