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Fisetin Promotes Hair Growth by Augmenting TERT Expression
Although thinning hair and alopecia are not recognized as severe diseases, hair loss has implications for mental health and quality of life; therefore, a large number of studies have been carried out to develop novel hair growth agents. In the present study, we aimed to examine the potential of telo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593534/ https://www.ncbi.nlm.nih.gov/pubmed/33178686 http://dx.doi.org/10.3389/fcell.2020.566617 |
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author | Kubo, Chisato Ogawa, Mizuki Uehara, Norihisa Katakura, Yoshinori |
author_facet | Kubo, Chisato Ogawa, Mizuki Uehara, Norihisa Katakura, Yoshinori |
author_sort | Kubo, Chisato |
collection | PubMed |
description | Although thinning hair and alopecia are not recognized as severe diseases, hair loss has implications for mental health and quality of life; therefore, a large number of studies have been carried out to develop novel hair growth agents. In the present study, we aimed to examine the potential of telomerase reverse transcriptase (TERT), because TERT overexpression in skin activates resting hair follicle bulge stem cells, which triggers initiation of a new hair follicle growth phase and promotes hair synthesis. To this end, we screened polyphenols that activate TERT expression in keratinocytes, and identified resveratrol and fisetin as strong hTERT-augmenting compounds. These polyphenols also regulated the gene expression of cytokines such as IGF-1 and KGF, which activate the β-catenin pathway, and TGF-β1, which plays an important role in maintaining the niche of hair follicle stem cells, thus are thought to play roles in promoting hair growth. We additionally showed that these polyphenols, especially fisetin, promoted hair growth from the shaved dorsal skin of mice, which suggests that these polyphenols activate the transition from telogen to anagen phase. Histological studies indicated that the dorsal skin of mice treated with these polyphenols contained numerous hair follicles and was thickened compared with that in control mice. Furthermore, on the dorsal skin of mice treated with resveratrol and fisetin, a number of proliferating cells (Ki67(+) cells) were observed around the hair papilla. These results suggest that resveratrol and fisetin induce a shift from telogen to anagen in the hair follicle by inducing proliferation of hair follicle bulge stem cells, thus promoting hair growth. |
format | Online Article Text |
id | pubmed-7593534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75935342020-11-10 Fisetin Promotes Hair Growth by Augmenting TERT Expression Kubo, Chisato Ogawa, Mizuki Uehara, Norihisa Katakura, Yoshinori Front Cell Dev Biol Cell and Developmental Biology Although thinning hair and alopecia are not recognized as severe diseases, hair loss has implications for mental health and quality of life; therefore, a large number of studies have been carried out to develop novel hair growth agents. In the present study, we aimed to examine the potential of telomerase reverse transcriptase (TERT), because TERT overexpression in skin activates resting hair follicle bulge stem cells, which triggers initiation of a new hair follicle growth phase and promotes hair synthesis. To this end, we screened polyphenols that activate TERT expression in keratinocytes, and identified resveratrol and fisetin as strong hTERT-augmenting compounds. These polyphenols also regulated the gene expression of cytokines such as IGF-1 and KGF, which activate the β-catenin pathway, and TGF-β1, which plays an important role in maintaining the niche of hair follicle stem cells, thus are thought to play roles in promoting hair growth. We additionally showed that these polyphenols, especially fisetin, promoted hair growth from the shaved dorsal skin of mice, which suggests that these polyphenols activate the transition from telogen to anagen phase. Histological studies indicated that the dorsal skin of mice treated with these polyphenols contained numerous hair follicles and was thickened compared with that in control mice. Furthermore, on the dorsal skin of mice treated with resveratrol and fisetin, a number of proliferating cells (Ki67(+) cells) were observed around the hair papilla. These results suggest that resveratrol and fisetin induce a shift from telogen to anagen in the hair follicle by inducing proliferation of hair follicle bulge stem cells, thus promoting hair growth. Frontiers Media S.A. 2020-10-15 /pmc/articles/PMC7593534/ /pubmed/33178686 http://dx.doi.org/10.3389/fcell.2020.566617 Text en Copyright © 2020 Kubo, Ogawa, Uehara and Katakura. 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 | Cell and Developmental Biology Kubo, Chisato Ogawa, Mizuki Uehara, Norihisa Katakura, Yoshinori Fisetin Promotes Hair Growth by Augmenting TERT Expression |
title | Fisetin Promotes Hair Growth by Augmenting TERT Expression |
title_full | Fisetin Promotes Hair Growth by Augmenting TERT Expression |
title_fullStr | Fisetin Promotes Hair Growth by Augmenting TERT Expression |
title_full_unstemmed | Fisetin Promotes Hair Growth by Augmenting TERT Expression |
title_short | Fisetin Promotes Hair Growth by Augmenting TERT Expression |
title_sort | fisetin promotes hair growth by augmenting tert expression |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593534/ https://www.ncbi.nlm.nih.gov/pubmed/33178686 http://dx.doi.org/10.3389/fcell.2020.566617 |
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