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Mycophenolate Antagonizes IFN-γ-Induced Catagen-Like Changes via β-Catenin Activation in Human Dermal Papilla Cells and Hair Follicles

Recently, various immunosuppressant drugs have been shown to induce hair growth in normal hair as well as in alopecia areata and androgenic alopecia; however, the responsible mechanism has not yet been fully elucidated. In this study, we investigate the influence of mycophenolate (MPA), an immunosup...

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Autores principales: Ryu, Sunhyo, Lee, Yonghee, Hyun, Moo Yeol, Choi, Sun Young, Jeong, Kwan Ho, Park, Young Min, Kang, Hoon, Park, Kui Young, Armstrong, Cheryl A., Johnson, Andrew, Song, Peter I., Kim, Beom Joon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4200814/
https://www.ncbi.nlm.nih.gov/pubmed/25247578
http://dx.doi.org/10.3390/ijms150916800
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author Ryu, Sunhyo
Lee, Yonghee
Hyun, Moo Yeol
Choi, Sun Young
Jeong, Kwan Ho
Park, Young Min
Kang, Hoon
Park, Kui Young
Armstrong, Cheryl A.
Johnson, Andrew
Song, Peter I.
Kim, Beom Joon
author_facet Ryu, Sunhyo
Lee, Yonghee
Hyun, Moo Yeol
Choi, Sun Young
Jeong, Kwan Ho
Park, Young Min
Kang, Hoon
Park, Kui Young
Armstrong, Cheryl A.
Johnson, Andrew
Song, Peter I.
Kim, Beom Joon
author_sort Ryu, Sunhyo
collection PubMed
description Recently, various immunosuppressant drugs have been shown to induce hair growth in normal hair as well as in alopecia areata and androgenic alopecia; however, the responsible mechanism has not yet been fully elucidated. In this study, we investigate the influence of mycophenolate (MPA), an immunosuppressant, on the proliferation of human dermal papilla cells (hDPCs) and on the growth of human hair follicles following catagen induction with interferon (IFN)-γ. IFN-γ was found to reduce β-catenin, an activator of hair follicle growth, and activate glycogen synthase kinase (GSK)-3β, and enhance expression of the Wnt inhibitor DKK-1 and catagen inducer transforming growth factor (TGF)-β2. IFN-γ inhibited expression of ALP and other dermal papillar cells (DPCs) markers such as Axin2, IGF-1, and FGF 7 and 10. MPA increased β-catenin in IFN-γ-treated hDPCs leading to its nuclear accumulation via inhibition of GSK3β and reduction of DKK-1. Furthermore, MPA significantly increased expression of ALP and other DPC marker genes but inhibited expression of TGF-β2. Therefore, we demonstrate for the first time that IFN-γ induces catagen-like changes in hDPCs and in hair follicles via inhibition of Wnt/β-catenin signaling, and that MPA stabilizes β-catenin by inhibiting GSK3β leading to increased β-catenin target gene and DP signature gene expression, which may, in part, counteract IFN-γ-induced catagen in hDPCs.
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spelling pubmed-42008142014-10-17 Mycophenolate Antagonizes IFN-γ-Induced Catagen-Like Changes via β-Catenin Activation in Human Dermal Papilla Cells and Hair Follicles Ryu, Sunhyo Lee, Yonghee Hyun, Moo Yeol Choi, Sun Young Jeong, Kwan Ho Park, Young Min Kang, Hoon Park, Kui Young Armstrong, Cheryl A. Johnson, Andrew Song, Peter I. Kim, Beom Joon Int J Mol Sci Article Recently, various immunosuppressant drugs have been shown to induce hair growth in normal hair as well as in alopecia areata and androgenic alopecia; however, the responsible mechanism has not yet been fully elucidated. In this study, we investigate the influence of mycophenolate (MPA), an immunosuppressant, on the proliferation of human dermal papilla cells (hDPCs) and on the growth of human hair follicles following catagen induction with interferon (IFN)-γ. IFN-γ was found to reduce β-catenin, an activator of hair follicle growth, and activate glycogen synthase kinase (GSK)-3β, and enhance expression of the Wnt inhibitor DKK-1 and catagen inducer transforming growth factor (TGF)-β2. IFN-γ inhibited expression of ALP and other dermal papillar cells (DPCs) markers such as Axin2, IGF-1, and FGF 7 and 10. MPA increased β-catenin in IFN-γ-treated hDPCs leading to its nuclear accumulation via inhibition of GSK3β and reduction of DKK-1. Furthermore, MPA significantly increased expression of ALP and other DPC marker genes but inhibited expression of TGF-β2. Therefore, we demonstrate for the first time that IFN-γ induces catagen-like changes in hDPCs and in hair follicles via inhibition of Wnt/β-catenin signaling, and that MPA stabilizes β-catenin by inhibiting GSK3β leading to increased β-catenin target gene and DP signature gene expression, which may, in part, counteract IFN-γ-induced catagen in hDPCs. MDPI 2014-09-22 /pmc/articles/PMC4200814/ /pubmed/25247578 http://dx.doi.org/10.3390/ijms150916800 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Ryu, Sunhyo
Lee, Yonghee
Hyun, Moo Yeol
Choi, Sun Young
Jeong, Kwan Ho
Park, Young Min
Kang, Hoon
Park, Kui Young
Armstrong, Cheryl A.
Johnson, Andrew
Song, Peter I.
Kim, Beom Joon
Mycophenolate Antagonizes IFN-γ-Induced Catagen-Like Changes via β-Catenin Activation in Human Dermal Papilla Cells and Hair Follicles
title Mycophenolate Antagonizes IFN-γ-Induced Catagen-Like Changes via β-Catenin Activation in Human Dermal Papilla Cells and Hair Follicles
title_full Mycophenolate Antagonizes IFN-γ-Induced Catagen-Like Changes via β-Catenin Activation in Human Dermal Papilla Cells and Hair Follicles
title_fullStr Mycophenolate Antagonizes IFN-γ-Induced Catagen-Like Changes via β-Catenin Activation in Human Dermal Papilla Cells and Hair Follicles
title_full_unstemmed Mycophenolate Antagonizes IFN-γ-Induced Catagen-Like Changes via β-Catenin Activation in Human Dermal Papilla Cells and Hair Follicles
title_short Mycophenolate Antagonizes IFN-γ-Induced Catagen-Like Changes via β-Catenin Activation in Human Dermal Papilla Cells and Hair Follicles
title_sort mycophenolate antagonizes ifn-γ-induced catagen-like changes via β-catenin activation in human dermal papilla cells and hair follicles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4200814/
https://www.ncbi.nlm.nih.gov/pubmed/25247578
http://dx.doi.org/10.3390/ijms150916800
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