Cytochrome P45011B1 (11 beta-hydroxylase) was detected in the human adrenal cortex and in human adenomas by in situ hybridization methods. Specific riboprobes were generated by in vitro transcription of 11 beta-hydroxylase--specific synthetic oligonucleotides with attached T7 and SP6 polymerase promotors. [35S]- and digoxigenin-labeled riboprobes were hybridized to sections of an aldosterone-producing adenoma (APA), the non-tumour portion of the corresponding adrenal gland, and two adenomas not related to hyperaldosteronism using standard protocols and varying washing conditions. After exposure of the radiolabeled sections to X-ray film, the signals were quantified and compared by statistical tests. Following autoradiography or immunohistochemical detection of the digoxigenin cytochrome P45011B1 mRNA was clearly localized in the zona fasciculata/reticularis of non-tumour portion of an human adrenal with an APA. Zona glomerulosa, medulla and connective tissue were free of label. As revealed by the semi-quantitative analysis, 11 beta-hydroxylase mRNA signals in the APA were significantly lower than those in the attached non-tumour portion and the other two adenomas. The results confirm known observations on the occurrence of cytochrome P45011B1 in the adrenal cortex of other species, but show, contrary to several immunohistochemical studies, that the enzyme is obviously not expressed in the zona glomerulosa.

Download full-text PDF

Source
http://dx.doi.org/10.1007/BF01464326DOI Listing

Publication Analysis

Top Keywords

cytochrome p45011b1
16
human adrenal
12
non-tumour portion
12
adrenal cortex
8
zona glomerulosa
8
adrenal
5
zone-specific localization
4
cytochrome
4
localization cytochrome
4
p45011b1
4

Similar Publications

Other conceivable renditions of some of the oxidative processes used in the biosynthesis of steroid hormones.

J Steroid Biochem Mol Biol

September 2006

Department of Obstetrics and Gynecology, Institute for Health Sciences, St. Luke's-Roosevelt Hospital Center, 432 West 58 Street, New York, NY 10019, USA.

Article Synopsis
  • The generally accepted version (GAV) of steroid hormone biosynthesis is based on artificial lab experiments and may not accurately reflect what happens in living organisms (in vivo), relying on untested assumptions that create uncertainty.
  • This text proposes alternative processes in steroid hormone production, suggesting that cytochrome P-450 enzymes introduce dioxygen into precursors to create reactive oxygen species instead of stable hydroxylated compounds as traditionally thought.
  • The new model implies specific oxygenated species act as intermediates for producing different hormones, which may help in understanding genetic enzyme deficiencies related to adrenal and ovarian function.
View Article and Find Full Text PDF

Cytochrome P45011B1 (11 beta-hydroxylase) was detected in the brain of male rats by in situ hybridization methods. Normal Sprague-Dawley rats were compared to the transgenic strain TGR(mRen2)27, characterized by the expression of the murine Ren-2d renin gene and the development of severe hypertension. Specific riboprobes were generated by in the vitro transcription of a 152 base-pair long cDNA template 35S-labeled riboprobes were hybridized to cryostat sections from adrenal glands and from two different levels of the brain using standard protocols and varying washing conditions.

View Article and Find Full Text PDF

Cytochrome P45011B1 (11 beta-hydroxylase) was detected in the human adrenal cortex and in human adenomas by in situ hybridization methods. Specific riboprobes were generated by in vitro transcription of 11 beta-hydroxylase--specific synthetic oligonucleotides with attached T7 and SP6 polymerase promotors. [35S]- and digoxigenin-labeled riboprobes were hybridized to sections of an aldosterone-producing adenoma (APA), the non-tumour portion of the corresponding adrenal gland, and two adenomas not related to hyperaldosteronism using standard protocols and varying washing conditions.

View Article and Find Full Text PDF

V79 Chinese hamster cells are being genetically engineered to express human mitochondrial cytochromes P450 as an analytical tool for studying adrenal steroid synthesis. Here, a V79 derived cell line is presented expressing the enzymatically active human cytochrome P45011B1 (CYP11B1) in a stable and constitutive manner. Full length CYP11B1 cDNA was obtained from surgically removed normal adrenal gland by polymerase chain reaction.

View Article and Find Full Text PDF

CYP11B1 was detected in the human adrenal cortex and in human adenomas by in situ-hybridization methods. Specific riboprobes were generated and hybridized to sections of an Aldosterone Producing Adenoma (APA), the non-tumour portion of the corresponding adrenal gland and two adenomas not related to hyperaldosteronism. P45011B1 mRNA was clearly localized in the zona fasciculata/reticularis.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!