首页> 美国卫生研究院文献>Tissue Engineering and Regenerative Medicine >MiR-214 Regulates the Human Hair Follicle Stem Cell Proliferation and Differentiation by Targeting EZH2 and Wnt/β-Catenin Signaling Way In Vitro
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MiR-214 Regulates the Human Hair Follicle Stem Cell Proliferation and Differentiation by Targeting EZH2 and Wnt/β-Catenin Signaling Way In Vitro

机译:MiR-214通过靶向EZH2和Wnt /β-Catenin信号传导途径体外调控人毛囊干细胞的增殖和分化

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摘要

miR-214 plays a major role in the self-renewal of skin tissue. However, whether miR-214 regulates the proliferation and differentiation of human hair follicle stem cells (HFSCs) is unknown. Primary HFSCs were isolated from human scalp skin tissue, cultured, and identified using flow cytometry. An miR-214 mimic and inhibitor were constructed for transfection into HFSCs. The MTS and colony formation assays examined cell proliferation. Immunofluorescence detected the localization and expression levels of TCF4, β-catenin, and differentiation markers. Luciferase reporter and TOP/FOP Flash assays investigated whether miR-214 targeted EZH2 and regulated the Wnt/β-catenin signaling pathway. Western blot determined the expression levels of enhancer of zeste homolog 2 (EZH2), Wnt/β-catenin signaling-related proteins, and HFSC differentiation markers in cells subjected to miR-214 transfection. miR-214 expression was remarkably decreased during the proliferation and differentiation of HFSCs into transit-amplifying (TA) cells. Downregulation of miR-214 promotes the proliferation and differentiation of HFSCs. Overexpression of miR-214 led to decreased expression of EZH2, β-catenin, and TCF-4, whereas downregulation of miR-214 resulted in increased expression of EZH2, β-catenin, and TCF-4 as well as TA differentiation markers. Immunofluorescence assay revealed that inhibiting miR-214 triggered the entry of β-catenin and TCF-4 into the nucleus. The luciferase reporter and TOP/FOP Flash assays demonstrated that miR-214 directly targets EZH2 and affects Wnt/β-catenin signaling. The miR-214/EZH2/β-catenin axis could be considered a candidate target in tissue engineering and regenerative medicine for HFSCs.
机译:miR-214在皮肤组织的自我更新中起主要作用。但是,miR-214是否调节人类毛囊干细胞(HFSCs)的增殖和分化尚不清楚。从人头皮皮肤组织中分离出原发性HFSC,进行培养并使用流式细胞仪进行鉴定。构建了miR-214模拟物和抑制剂,用于转染到HFSC中。 MTS和集落形成测定法检查了细胞增殖。免疫荧光检测TCF4,β-catenin和分化标志物的定位和表达水平。萤光素酶报道基因和TOP / FOP Flash分析研究了miR-214是否靶向EZH2并调节Wnt /β-catenin信号通路。 Western印迹法确定了在进行miR-214转染的细胞中zeste同源物2(EZH2),Wnt /β-catenin信号传导相关蛋白和HFSC分化标记的增强子的表达水平。在HFSC增殖和分化为转运扩增(TA)细胞的过程中,miR-214的表达明显降低。 miR-214的下调促进了HFSC的增殖和分化。 miR-214的过表达导致EZH2,β-catenin和TCF-4的表达降低,而miR-214的下调导致EZH2,β-catenin和TCF-4以及TA分化标记的表达增加。免疫荧光分析显示,抑制miR-214会触发β-catenin和TCF-4进入细胞核。荧光素酶报告基因和TOP / FOP Flash分析表明,miR-214直接靶向EZH2,并影响Wnt /β-catenin信号传导。可以将miR-214 / EZH2 /β-catenin轴视为HFSCs的组织工程和再生医学的候选靶标。

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