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

被引:16
作者
Cai, Bingjie [1 ]
Li, Min [2 ]
Zheng, Yunpeng [1 ]
Yin, Yakun [1 ]
Jin, Fangcao [1 ]
Li, Xuyang [1 ]
Dong, Juan [1 ]
Jiao, Xiaoyan [1 ]
Liu, Xiaojun [3 ]
Zhang, Kun [4 ]
Li, Dongqin [1 ]
Wang, Junmin [5 ]
Yin, Guangwen [1 ]
机构
[1] Zhengzhou Univ, Dept Dermatol, Affiliated Hosp 1, Zhengzhou 450052, Peoples R China
[2] Henan Prov Peoples Hosp, Dept Dermatol, Zhengzhou 450003, Peoples R China
[3] Henan Prov Med Instrument Testing Inst, Zhengzhou 450018, Peoples R China
[4] Zhengzhou Univ, Sch Life Sci, Zhengzhou 450001, Peoples R China
[5] Zhengzhou Univ, Dept Anat, Coll Basic Med Sci, Zhengzhou 450000, Peoples R China
来源
AGING-US | 2020年 / 12卷 / 13期
关键词
hair growth; EZH2; microRNA-22; STK40; hair follicle stem cell differentiation; TRANSIT-AMPLIFYING CELLS; WNT/BETA-CATENIN; APOPTOSIS; PATHWAY; MEF2; EZH2;
D O I
10.18632/aging.103165
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:12726 / 12739
页数:14
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