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Dihydrotestosterone Regulates Hair Growth Through the Wnt/β-Catenin Pathway in C57BL/6 Mice and In Vitro Organ Culture

Dihydrotestosterone (DHT) is the most potent androgen that regulates hair cycling. Hair cycling involves cross-talk between the androgen and Wnt/β-catenin pathways. However, how DHT regulates hair follicle (HF) growth through the Wnt/β-catenin pathway has not been well investigated. This study aimed...

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Autores principales: Chen, Xianyan, Liu, Ben, Li, Ying, Han, Le, Tang, Xin, Deng, Wenjia, Lai, Wei, Wan, Miaojian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6989660/
https://www.ncbi.nlm.nih.gov/pubmed/32038233
http://dx.doi.org/10.3389/fphar.2019.01528
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author Chen, Xianyan
Liu, Ben
Li, Ying
Han, Le
Tang, Xin
Deng, Wenjia
Lai, Wei
Wan, Miaojian
author_facet Chen, Xianyan
Liu, Ben
Li, Ying
Han, Le
Tang, Xin
Deng, Wenjia
Lai, Wei
Wan, Miaojian
author_sort Chen, Xianyan
collection PubMed
description Dihydrotestosterone (DHT) is the most potent androgen that regulates hair cycling. Hair cycling involves cross-talk between the androgen and Wnt/β-catenin pathways. However, how DHT regulates hair follicle (HF) growth through the Wnt/β-catenin pathway has not been well investigated. This study aimed to investigate the roles of DHT in hair growth in vivo and in vitro. Human scalp HFs were treated with different concentrations of DHT (10(-5), 10(-6), 10(-7), 10(-8), and 10(-9) mol/L) for 10 days. The effects of DHT on hair shaft elongation, the proliferation of hair matrix cells, and the levels of β-catenin, GSK-3β, and phosphorylated GSK-3β (ser9) were evaluated in the cultured HFs. The effects of DHT were further investigated in C57BL/6 mice. Moreover, the growth of cultured human HFs was observed after interfering with the β-catenin pathway through inhibitors or activators in the presence or absence of DHT. We found that different concentrations of DHT had different effects on human HFs in vitro and C57BL/6 mice. At 10(-6) mol/L, DHT inhibited HF growth and β-catenin/p-GSK-3β expression, whereas 10(-7) mol/L DHT induced HF growth and β-catenin/p-GSK-3β expression. In addition, a β-catenin inhibitor (21H7) inhibited HF growth in vitro, while a β-catenin activator (IM12) promoted HF growth in vitro and antagonized the inhibition of HFs by high levels of DHT. These results suggest that DHT plays a pivotal role in region-specific hair growth, which may be related to the Wnt/β-catenin pathway.
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spelling pubmed-69896602020-02-07 Dihydrotestosterone Regulates Hair Growth Through the Wnt/β-Catenin Pathway in C57BL/6 Mice and In Vitro Organ Culture Chen, Xianyan Liu, Ben Li, Ying Han, Le Tang, Xin Deng, Wenjia Lai, Wei Wan, Miaojian Front Pharmacol Pharmacology Dihydrotestosterone (DHT) is the most potent androgen that regulates hair cycling. Hair cycling involves cross-talk between the androgen and Wnt/β-catenin pathways. However, how DHT regulates hair follicle (HF) growth through the Wnt/β-catenin pathway has not been well investigated. This study aimed to investigate the roles of DHT in hair growth in vivo and in vitro. Human scalp HFs were treated with different concentrations of DHT (10(-5), 10(-6), 10(-7), 10(-8), and 10(-9) mol/L) for 10 days. The effects of DHT on hair shaft elongation, the proliferation of hair matrix cells, and the levels of β-catenin, GSK-3β, and phosphorylated GSK-3β (ser9) were evaluated in the cultured HFs. The effects of DHT were further investigated in C57BL/6 mice. Moreover, the growth of cultured human HFs was observed after interfering with the β-catenin pathway through inhibitors or activators in the presence or absence of DHT. We found that different concentrations of DHT had different effects on human HFs in vitro and C57BL/6 mice. At 10(-6) mol/L, DHT inhibited HF growth and β-catenin/p-GSK-3β expression, whereas 10(-7) mol/L DHT induced HF growth and β-catenin/p-GSK-3β expression. In addition, a β-catenin inhibitor (21H7) inhibited HF growth in vitro, while a β-catenin activator (IM12) promoted HF growth in vitro and antagonized the inhibition of HFs by high levels of DHT. These results suggest that DHT plays a pivotal role in region-specific hair growth, which may be related to the Wnt/β-catenin pathway. Frontiers Media S.A. 2020-01-23 /pmc/articles/PMC6989660/ /pubmed/32038233 http://dx.doi.org/10.3389/fphar.2019.01528 Text en Copyright © 2020 Chen, Liu, Li, Han, Tang, Deng, Lai and Wan http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Chen, Xianyan
Liu, Ben
Li, Ying
Han, Le
Tang, Xin
Deng, Wenjia
Lai, Wei
Wan, Miaojian
Dihydrotestosterone Regulates Hair Growth Through the Wnt/β-Catenin Pathway in C57BL/6 Mice and In Vitro Organ Culture
title Dihydrotestosterone Regulates Hair Growth Through the Wnt/β-Catenin Pathway in C57BL/6 Mice and In Vitro Organ Culture
title_full Dihydrotestosterone Regulates Hair Growth Through the Wnt/β-Catenin Pathway in C57BL/6 Mice and In Vitro Organ Culture
title_fullStr Dihydrotestosterone Regulates Hair Growth Through the Wnt/β-Catenin Pathway in C57BL/6 Mice and In Vitro Organ Culture
title_full_unstemmed Dihydrotestosterone Regulates Hair Growth Through the Wnt/β-Catenin Pathway in C57BL/6 Mice and In Vitro Organ Culture
title_short Dihydrotestosterone Regulates Hair Growth Through the Wnt/β-Catenin Pathway in C57BL/6 Mice and In Vitro Organ Culture
title_sort dihydrotestosterone regulates hair growth through the wnt/β-catenin pathway in c57bl/6 mice and in vitro organ culture
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6989660/
https://www.ncbi.nlm.nih.gov/pubmed/32038233
http://dx.doi.org/10.3389/fphar.2019.01528
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