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EZH2-mediated inhibition of microRNA-22 promotes differentiation of hair follicle stem cells by elevating STK40 expression

Hair follicle stem cells (HFSCs) contribute to the regeneration of hair follicles (HFs), thus accelerating hair growth. microRNAs (miRs) are potential regulators in various cellular processes, including HFSC proliferation and differentiation. This study proposed a potential target, enhancer of zeste...

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Autores principales: Cai, Bingjie, Li, Min, Zheng, Yunpeng, Yin, Yakun, Jin, Fangcao, Li, Xuyang, Dong, Juan, Jiao, Xiaoyan, Liu, Xiaojun, Zhang, Kun, Li, Dongqin, Wang, Junmin, Yin, Guangwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377840/
https://www.ncbi.nlm.nih.gov/pubmed/32657761
http://dx.doi.org/10.18632/aging.103165
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author Cai, Bingjie
Li, Min
Zheng, Yunpeng
Yin, Yakun
Jin, Fangcao
Li, Xuyang
Dong, Juan
Jiao, Xiaoyan
Liu, Xiaojun
Zhang, Kun
Li, Dongqin
Wang, Junmin
Yin, Guangwen
author_facet Cai, Bingjie
Li, Min
Zheng, Yunpeng
Yin, Yakun
Jin, Fangcao
Li, Xuyang
Dong, Juan
Jiao, Xiaoyan
Liu, Xiaojun
Zhang, Kun
Li, Dongqin
Wang, Junmin
Yin, Guangwen
author_sort Cai, Bingjie
collection PubMed
description Hair follicle stem cells (HFSCs) contribute to the regeneration of hair follicles (HFs), thus accelerating hair growth. microRNAs (miRs) are potential regulators in various cellular processes, including HFSC proliferation and differentiation. This study proposed a potential target, enhancer of zeste homolog 2 (EZH2) for facilitating hair growth, due to its function over HFSC activities by mediating the miR-22/serine/threonine kinase 40 (STK40)/myocyte enhancer factor 2 (MEF2)/alkaline phosphatase (ALP) axis. Gain- and loss-of-function approaches were adopted to explore the roles of EZH2, miR-22, and STK40 in the proliferation and apoptosis of HFSCs, along with the functional relevance of MEF2-ALP activity. STK40 was elevated during HFSC differentiation, which was found to facilitate HFSC proliferation, but impede their apoptosis by activating MEF2-ALP. Mechanically, miR-22 targeted and inversely regulated STK40, which inhibited MEF2-ALP activity to impede HFSC proliferation and differentiation. Moreover, EZH2 elevated the STK40 expression by repressing miR-22 to promote the proliferation and differentiation of HFSCs. Furthermore, in vivo experiments further validated the roles of EZH2 and STK40 on hair follicle neogenesis and hair growth. Collectively, EZH2 elevated the STK40 expression by downregulating miR-22, consequently accelerating differentiation of HFSCs and hair growth, which sheds light on the underlying molecular mechanism responsible for hair growth.
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spelling pubmed-73778402020-07-31 EZH2-mediated inhibition of microRNA-22 promotes differentiation of hair follicle stem cells by elevating STK40 expression Cai, Bingjie Li, Min Zheng, Yunpeng Yin, Yakun Jin, Fangcao Li, Xuyang Dong, Juan Jiao, Xiaoyan Liu, Xiaojun Zhang, Kun Li, Dongqin Wang, Junmin Yin, Guangwen Aging (Albany NY) Research Paper Hair follicle stem cells (HFSCs) contribute to the regeneration of hair follicles (HFs), thus accelerating hair growth. microRNAs (miRs) are potential regulators in various cellular processes, including HFSC proliferation and differentiation. This study proposed a potential target, enhancer of zeste homolog 2 (EZH2) for facilitating hair growth, due to its function over HFSC activities by mediating the miR-22/serine/threonine kinase 40 (STK40)/myocyte enhancer factor 2 (MEF2)/alkaline phosphatase (ALP) axis. Gain- and loss-of-function approaches were adopted to explore the roles of EZH2, miR-22, and STK40 in the proliferation and apoptosis of HFSCs, along with the functional relevance of MEF2-ALP activity. STK40 was elevated during HFSC differentiation, which was found to facilitate HFSC proliferation, but impede their apoptosis by activating MEF2-ALP. Mechanically, miR-22 targeted and inversely regulated STK40, which inhibited MEF2-ALP activity to impede HFSC proliferation and differentiation. Moreover, EZH2 elevated the STK40 expression by repressing miR-22 to promote the proliferation and differentiation of HFSCs. Furthermore, in vivo experiments further validated the roles of EZH2 and STK40 on hair follicle neogenesis and hair growth. Collectively, EZH2 elevated the STK40 expression by downregulating miR-22, consequently accelerating differentiation of HFSCs and hair growth, which sheds light on the underlying molecular mechanism responsible for hair growth. Impact Journals 2020-07-12 /pmc/articles/PMC7377840/ /pubmed/32657761 http://dx.doi.org/10.18632/aging.103165 Text en Copyright © 2020 Cai et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Cai, Bingjie
Li, Min
Zheng, Yunpeng
Yin, Yakun
Jin, Fangcao
Li, Xuyang
Dong, Juan
Jiao, Xiaoyan
Liu, Xiaojun
Zhang, Kun
Li, Dongqin
Wang, Junmin
Yin, Guangwen
EZH2-mediated inhibition of microRNA-22 promotes differentiation of hair follicle stem cells by elevating STK40 expression
title EZH2-mediated inhibition of microRNA-22 promotes differentiation of hair follicle stem cells by elevating STK40 expression
title_full EZH2-mediated inhibition of microRNA-22 promotes differentiation of hair follicle stem cells by elevating STK40 expression
title_fullStr EZH2-mediated inhibition of microRNA-22 promotes differentiation of hair follicle stem cells by elevating STK40 expression
title_full_unstemmed EZH2-mediated inhibition of microRNA-22 promotes differentiation of hair follicle stem cells by elevating STK40 expression
title_short EZH2-mediated inhibition of microRNA-22 promotes differentiation of hair follicle stem cells by elevating STK40 expression
title_sort ezh2-mediated inhibition of microrna-22 promotes differentiation of hair follicle stem cells by elevating stk40 expression
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377840/
https://www.ncbi.nlm.nih.gov/pubmed/32657761
http://dx.doi.org/10.18632/aging.103165
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