8365357

pubmed:Citation

3

The sexually dimorphic pattern of GH secretion regulates the expression of several steroidogenic enzymes in rat liver, including a male-specific 3 beta-hydroxysteroid dehydrogenase/delta 5-->4-isomerase (3 beta HSD). Recently, we identified male-specific isoforms of immunoreactive 3 beta HSD in mouse liver [42 kilodaltons (kDa)] and gonads (47 kDa). To test whether GH can regulate the expression of these murine 3 beta HSDs, endogenous forms of 3 beta HSD were studied in transgenic mice expressing heterologous GH transgene products. Mice from five transgenic lines were used; two expressed GH transgenes encoding the phosphoenolpyruvate carboxykinase (PEPCK) promoter fused to either the human (h) GH (somatogenic and lactogenic) or bovine (b) GH (somatogenic) structural genes, and three expressed GH transgenes encoding the mouse metallothionein-1 (MT1) promoter fused to the hGH, hGH variant (hGHv), or bGH structural genes. Control mice were normal nontransgenic littermates. Expression of a male-specific (42 kDa) isoform of hepatic 3 beta HSD is dramatically suppressed in all transgenic mouse lines, as detected on Western immunoblots, without affecting a 47-kDa isoform expressed in livers of both male and female mice. This negative regulation was not observed in mouse kidney, which normally expresses two 3 beta HSD isoforms (in both sexes) with molecular masses similar to those in liver. Considering that PEPCK and MT1 promoters direct expression of GH fusion genes in both tissues, the inhibition of hepatic, but not renal, 3 beta HSD immunoreactivity suggests that GH affects sex-specific, rather than tissue-specific, expression of 3 beta HSD. As in the liver, sex-specific expression of 3 beta HSD in the testis is also suppressed by heterologous GH, but with one notable difference. Only human-derived GH (MT1-hGH and MT1-hGHv) effectively inhibits expression of the 47-kDa sex-specific isoform of testicular 3 beta HSD, without affecting the 44-kDa isoform expressed in gonads of both male and female mice. These results suggest that the negative effects of heterologous GH on sex-specific 3 beta HSDs may be mediated by PRL receptors in the testis and GH receptors in the liver. PEPCK-GH transgenes had little effect on testicular 3 beta HSD, possibly because this promoter (unlike MT1) is relatively inactive in this tissue. In the liver of male transgenics (PEPCK-hGH), loss of the sex-specific (42-kDa) 3 beta HSD has little effect on the Km for dehydroepiandrosterone (DHEA; 11 microM) compared with that in normal controls (16 microM).(ABSTRACT TRUNCATED AT 400 WORDS)

eng

AIM

MEDLINE

0013-7227

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NLM

1131-8

pubmed-meshheading:8365357-Animals, pubmed-meshheading:8365357-Base Sequence, pubmed-meshheading:8365357-Female, pubmed-meshheading:8365357-Gene Expression Regulation, pubmed-meshheading:8365357-Growth Hormone, pubmed-meshheading:8365357-Isoenzymes, pubmed-meshheading:8365357-Liver, pubmed-meshheading:8365357-Male, pubmed-meshheading:8365357-Metallothionein, pubmed-meshheading:8365357-Mice, pubmed-meshheading:8365357-Mice, Inbred C3H, pubmed-meshheading:8365357-Mice, Inbred C57BL, pubmed-meshheading:8365357-Mice, Transgenic, pubmed-meshheading:8365357-Molecular Sequence Data, pubmed-meshheading:8365357-Multienzyme Complexes, pubmed-meshheading:8365357-NAD, pubmed-meshheading:8365357-Nucleic Acid Hybridization, pubmed-meshheading:8365357-Phosphoenolpyruvate Carboxykinase (GTP), pubmed-meshheading:8365357-Progesterone Reductase, pubmed-meshheading:8365357-RNA, Messenger, pubmed-meshheading:8365357-Recombinant Fusion Proteins, pubmed-meshheading:8365357-Sex Characteristics, pubmed-meshheading:8365357-Steroid Isomerases, pubmed-meshheading:8365357-Testis

Growth hormone transgenes regulate the expression of sex-specific isoforms of 3 beta-hydroxysteroid dehydrogenase/delta 5-->4-isomerase in mouse liver and gonads.

Journal Article, Comparative Study, Research Support, U.S. Gov't, P.H.S.