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Age and skin site related differences in steroid metabolism in male skin point to a key role of sebocytes in cutaneous hormone metabolism

Hormone concentrations decline with aging. Up to now it was not clear, whether the decrease of hormone concentrations in blood samples are also present in cutaneous suction blister fluids, and whether skin from different anatomical sites shows different hormone concentrations. Analysis of suction bl...

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Autores principales: Haag, Markus, Hamann, Tina, Kulle, Alexandra E., Riepe, Felix G., Blatt, Thomas, Wenck, Horst, Holterhus, Paul-Martin, Peirano, Reto Ivo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3408994/
https://www.ncbi.nlm.nih.gov/pubmed/22870354
http://dx.doi.org/10.4161/derm.19201
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author Haag, Markus
Hamann, Tina
Kulle, Alexandra E.
Riepe, Felix G.
Blatt, Thomas
Wenck, Horst
Holterhus, Paul-Martin
Peirano, Reto Ivo
author_facet Haag, Markus
Hamann, Tina
Kulle, Alexandra E.
Riepe, Felix G.
Blatt, Thomas
Wenck, Horst
Holterhus, Paul-Martin
Peirano, Reto Ivo
author_sort Haag, Markus
collection PubMed
description Hormone concentrations decline with aging. Up to now it was not clear, whether the decrease of hormone concentrations in blood samples are also present in cutaneous suction blister fluids, and whether skin from different anatomical sites shows different hormone concentrations. Analysis of suction blister fluids and paired blood samples from young (mean 27.8 y) and old (mean 62.6 y) male subjects by UPLC-MS/MS showed that DHEA concentration in blood samples was age-dependently significantly reduced, but increased in suction blister fluids, while androstenedione behaved in an opposite manner to DHEA. Testosterone decreased age-dependently in blood samples and in suction blister fluids. Regarding skin sites, DHEA was lower in samples from upper back compared with samples from the forearm. In contrast, the concentrations of androstenedione and testosterone were higher in samples from upper back. In vitro analyses showed that SZ95 sebocytes, but neither primary fibroblasts nor keratinocytes, were able to use DHEA as precursor for testosterone biosynthesis, which was confirmed by expression analysis of 3β-hydroxysteroiddehydrogenase in skin biopsies. In conclusion, we show an inverse pattern of DHEA and androstenedione concentrations in blood vs. suction blister fluids, highlighting age-dependent changes of dermal testosterone biosynthesis, and a stronger metabolism in young skin. Furthermore, sebocytes play a central role in cutaneous androgen metabolism.
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spelling pubmed-34089942012-08-06 Age and skin site related differences in steroid metabolism in male skin point to a key role of sebocytes in cutaneous hormone metabolism Haag, Markus Hamann, Tina Kulle, Alexandra E. Riepe, Felix G. Blatt, Thomas Wenck, Horst Holterhus, Paul-Martin Peirano, Reto Ivo Dermatoendocrinol Report Hormone concentrations decline with aging. Up to now it was not clear, whether the decrease of hormone concentrations in blood samples are also present in cutaneous suction blister fluids, and whether skin from different anatomical sites shows different hormone concentrations. Analysis of suction blister fluids and paired blood samples from young (mean 27.8 y) and old (mean 62.6 y) male subjects by UPLC-MS/MS showed that DHEA concentration in blood samples was age-dependently significantly reduced, but increased in suction blister fluids, while androstenedione behaved in an opposite manner to DHEA. Testosterone decreased age-dependently in blood samples and in suction blister fluids. Regarding skin sites, DHEA was lower in samples from upper back compared with samples from the forearm. In contrast, the concentrations of androstenedione and testosterone were higher in samples from upper back. In vitro analyses showed that SZ95 sebocytes, but neither primary fibroblasts nor keratinocytes, were able to use DHEA as precursor for testosterone biosynthesis, which was confirmed by expression analysis of 3β-hydroxysteroiddehydrogenase in skin biopsies. In conclusion, we show an inverse pattern of DHEA and androstenedione concentrations in blood vs. suction blister fluids, highlighting age-dependent changes of dermal testosterone biosynthesis, and a stronger metabolism in young skin. Furthermore, sebocytes play a central role in cutaneous androgen metabolism. Landes Bioscience 2012-01-01 /pmc/articles/PMC3408994/ /pubmed/22870354 http://dx.doi.org/10.4161/derm.19201 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Report
Haag, Markus
Hamann, Tina
Kulle, Alexandra E.
Riepe, Felix G.
Blatt, Thomas
Wenck, Horst
Holterhus, Paul-Martin
Peirano, Reto Ivo
Age and skin site related differences in steroid metabolism in male skin point to a key role of sebocytes in cutaneous hormone metabolism
title Age and skin site related differences in steroid metabolism in male skin point to a key role of sebocytes in cutaneous hormone metabolism
title_full Age and skin site related differences in steroid metabolism in male skin point to a key role of sebocytes in cutaneous hormone metabolism
title_fullStr Age and skin site related differences in steroid metabolism in male skin point to a key role of sebocytes in cutaneous hormone metabolism
title_full_unstemmed Age and skin site related differences in steroid metabolism in male skin point to a key role of sebocytes in cutaneous hormone metabolism
title_short Age and skin site related differences in steroid metabolism in male skin point to a key role of sebocytes in cutaneous hormone metabolism
title_sort age and skin site related differences in steroid metabolism in male skin point to a key role of sebocytes in cutaneous hormone metabolism
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3408994/
https://www.ncbi.nlm.nih.gov/pubmed/22870354
http://dx.doi.org/10.4161/derm.19201
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