Tissue Eng Regen Med.  2018 Jun;15(3):341-350. 10.1007/s13770-018-0118-x.

MiR-214 Regulates the Human Hair Follicle Stem Cell Proliferation and Differentiation by Targeting EZH2 and Wnt/β-Catenin Signaling Way In Vitro

Affiliations
  • 1Department of Rehabilitation, The First Affiliated Hospital, Jinan University, Guangzhou 510630, Guangdong, China.
  • 2Department of Rehabilitation, Chenzhou NO.1 People's Hospital, Chenzhou 423000, Hunan, China. pcheng83@sina.com mszrch3@163.com
  • 3Department of Plastic Surgery, The 3rd Xiangya Hospital, Central South University, Tongzipo Road NO.138, Changsha 410013, Hunan, China. pcheng83@sina.com
  • 4Department of Rehabilitation Medicine, Guangdong Geriatric Institute, Guangdong General Hospital & Guangdong Academy of Medical Sciences, Zhongshan 2nd Road NO.106, Guangzhou 510080, Guangdong, China. mszrch3@163.com

Abstract

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.

Keyword

miR-214; Hair follicles stem cells; Transit-amplifying cells; EZH2; Wnt/β-catenin signal

MeSH Terms

Antigens, Differentiation
Blotting, Western
Cell Proliferation
Down-Regulation
Flow Cytometry
Fluorescent Antibody Technique
Hair Follicle*
Hair*
Humans*
In Vitro Techniques*
Luciferases
Regenerative Medicine
Scalp
Skin
Stem Cells*
Tissue Engineering
Transfection
Antigens, Differentiation
Luciferases
Full Text Links
  • TERM
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr