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

机译:EzH2介导的MicroRNA-22的抑制通过升高STK40表达来促进毛囊干细胞的分化

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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, 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.
机译:毛发卵泡干细胞(HFSCs)有助于毛囊(HFS)的再生,从而加速毛发生生长。 MicroRNA(MIRS)是各种细胞过程中的潜在调节剂,包括HFSC增殖和分化。该研究提出了一种潜在的靶标,Zeste同源物2(EZH2)的增强剂,用于促进毛发生生长,由于其通过介导MIR-22 /丝氨酸/苏氨酸激酶40(STK40)/肌细胞增强子因子2(MEF2)而通过HFSC活性的功能/碱性磷酸酶(ALP)轴。采用增益和函数丧失方法来探讨EZH2,MIR-22和STK40在HFSCs的增殖和凋亡中的作用,以及MEF2-ALP活性的功能相关性。 STK40在HFSC分化期间升高,发现促进HFSC增殖,但通过激活MeF2-ALP妨碍它们的细胞凋亡。机械,miR-22靶向和反向调节的STK40,其抑制MEF2-ALP活性以阻止HFSC的增殖和分化。此外,EZH2通过抑制miR-22来升高STK40表达,以促进HFSCs的增殖和分化。此外,实验进一步验证了EzH2和STK40对毛囊新发生和毛发生生长的作用。通过下调miR-22,EZH2尤其升高了STK40表达,从而加速了HFSCs和毛发生生长的分化,其揭示了负责毛发生长的潜在分子机制。

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