11Beta-hydroxysteroid dehydrogenase type 2 and mineralocorticoid receptor in human fetal development

11Beta-Hydroxysteroid dehydrogenase type II (11betaHSD2) confers specificity on the mineralocorticoid receptor (MR) by converting biologically active glucocorticoids to inactive 11-keto metabolites. The biological significance of 11betaHSD2 activity during fetal development is currently being explor...

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Bibliographic Details
Published in:The journal of clinical endocrinology and metabolism 1999-04, Vol.84 (4), p.1453-1458
Main Authors: Hirasawa, G, Sasano, H, Suzuki, T, Takeyama, J, Muramatu, Y, Fukushima, K, Hiwatashi, N, Toyota, T, Nagura, H, Krozowski, Z S
Format: Article
Language:English
Subjects:
11-beta-Hydroxysteroid Dehydrogenases
Embryonic and Fetal Development
Female
Fetus - metabolism
Humans
Hydroxysteroid Dehydrogenases - metabolism
Immunohistochemistry
Kidney - chemistry
Liver - chemistry
Lung - chemistry
Pregnancy
Receptors, Mineralocorticoid - analysis
Skin - chemistry
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Summary:11Beta-Hydroxysteroid dehydrogenase type II (11betaHSD2) confers specificity on the mineralocorticoid receptor (MR) by converting biologically active glucocorticoids to inactive 11-keto metabolites. The biological significance of 11betaHSD2 activity during fetal development is currently being explored, but the temporal and spatial distributions of the enzyme and receptor have not been examined. We therefore examined their distributions during various stages of human fetal development using immunohistochemistry. Both 11betaHSD2 and MR immunoreactivity were detected in the distal convoluted and collecting tubules of the kidney from early in gestation. Fetal skin, intermediate layer of the epidermis, peridermal cells, and hair follicles were positive for both 11betaHSD2 and MR. Weak 11betaHSD2 and MR immunoreactivity was detected in the superficial ciliated epithelium of the esophagus, the deep layer of gastric epithelial cells, and the superficial epithelium of the small intestine. Columnar epithelium in the terminal bronchiolar budding component of fetal lung and tracheal and bronchial ciliated epithelium were also positive for MR and 11betaHSD2 from early gestation. Colonic epithelium and pancreatic exocrine duct cells, which demonstrated marked immunoreactivity of both MR and 11betaHSD2 in the adult, did not express MR and 11betaHSD2 until very late in gestation. These results imply that mineralocorticoid action in the upper fetal gastrointestinal tract, kidney, skin, and lung is facilitated by 11betaHSD2 and is involved in water and electrolyte transport between fetus and amniotic fluid as well as fetal urine production.
ISSN:0021-972X