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EZH2 介导的 microRNA-22 抑制通过提高 STK40 表达促进毛囊干细胞分化。

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

机构信息

Department of Dermatology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, P. R. China.

Department of Dermatology, Henan Provincial People's Hospital, Zhengzhou 450003, P. R. China.

出版信息

Aging (Albany NY). 2020 Jul 12;12(13):12726-12739. doi: 10.18632/aging.103165.


DOI:10.18632/aging.103165
PMID:32657761
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7377840/
Abstract

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.

摘要

毛囊干细胞 (HFSCs) 有助于毛囊 (HF) 的再生,从而加速头发生长。 microRNAs (miRs) 是各种细胞过程的潜在调节剂,包括 HFSC 的增殖和分化。本研究提出了一个潜在的靶标,增强子的外显子 2 (EZH2),由于其通过调节 miR-22/丝氨酸/苏氨酸激酶 40 (STK40)/肌细胞增强因子 2 (MEF2)/碱性磷酸酶 (ALP) 轴对 HFSC 活性的作用,促进头发生长。采用增益和缺失功能方法来探讨 EZH2、miR-22 和 STK40 在 HFSCs 增殖和凋亡中的作用,以及 MEF2-ALP 活性的功能相关性。STK40 在 HFSC 分化过程中升高,发现其通过激活 MEF2-ALP 促进 HFSC 增殖,但阻碍其凋亡。在机制上,miR-22 靶向并反向调节 STK40,抑制 MEF2-ALP 活性,从而阻碍 HFSC 的增殖和分化。此外,EZH2 通过抑制 miR-22 升高 STK40 的表达,促进 HFSCs 的增殖和分化。此外,实验进一步验证了 EZH2 和 STK40 在毛囊新生和头发生长中的作用。总之,EZH2 通过下调 miR-22 升高 STK40 的表达,从而加速 HFSCs 的分化和头发生长,这揭示了头发生长的潜在分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/77caee0a8f00/aging-12-103165-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/6179b41ddb8e/aging-12-103165-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/bc1634ccca96/aging-12-103165-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/fa0daf4b5ed3/aging-12-103165-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/633620a641cd/aging-12-103165-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/d5f8a0054c35/aging-12-103165-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/03164eb5afd8/aging-12-103165-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/010cd778efd6/aging-12-103165-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/29eb1b4ab7d7/aging-12-103165-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/77caee0a8f00/aging-12-103165-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/6179b41ddb8e/aging-12-103165-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/bc1634ccca96/aging-12-103165-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/fa0daf4b5ed3/aging-12-103165-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/633620a641cd/aging-12-103165-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/d5f8a0054c35/aging-12-103165-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/03164eb5afd8/aging-12-103165-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/010cd778efd6/aging-12-103165-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/29eb1b4ab7d7/aging-12-103165-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f5/7377840/77caee0a8f00/aging-12-103165-g009.jpg

相似文献

[1]
EZH2-mediated inhibition of microRNA-22 promotes differentiation of hair follicle stem cells by elevating STK40 expression.

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[4]
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Genes (Basel). 2023-1-27

[5]
Morphogenesis, Growth Cycle and Molecular Regulation of Hair Follicles.

Front Cell Dev Biol. 2022-5-12

[6]
Perspectives on miRNAs Targeting DKK1 for Developing Hair Regeneration Therapy.

Cells. 2021-10-30

[7]
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[8]
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[10]
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本文引用的文献

[1]
MiR-214 Regulates the Human Hair Follicle Stem Cell Proliferation and Differentiation by Targeting EZH2 and Wnt/β-Catenin Signaling Way .

Tissue Eng Regen Med. 2018-5-7

[2]
Activation of GPR55 increases neural stem cell proliferation and promotes early adult hippocampal neurogenesis.

Br J Pharmacol. 2018-7-4

[3]
Dysregulation of EZH2/miR-138 axis contributes to drug resistance in multiple myeloma by downregulating RBPMS.

Leukemia. 2018-4-24

[4]
EZH2 promotes hepatocellular carcinoma progression through modulating miR-22/galectin-9 axis.

J Exp Clin Cancer Res. 2018-1-9

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Immunohistochemical dissection of cystic panfolliculoma focusing on the expression of multiple hair follicle lineage markers with an insight into the pathogenesis.

J Cutan Pathol. 2017-10

[6]
The major miR-31 target genes STK40 and LATS2 and their implications in the regulation of keratinocyte growth and hair differentiation.

Exp Dermatol. 2017-6

[7]
microRNA-130a Promotes Human Keratinocyte Viability and Migration and Inhibits Apoptosis Through Direct Regulation of STK40-Mediated NF-κB Pathway and Indirect Regulation of SOX9-Meditated JNK/MAPK Pathway: A Potential Role in Psoriasis.

DNA Cell Biol. 2017-3

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Beta-catenin can induce hair follicle stem cell differentiation into transit-amplifying cells through c-myc activation.

Tissue Cell. 2017-2

[9]
Serine/Threonine Kinase 40 (Stk40) Functions as a Novel Regulator of Skeletal Muscle Differentiation.

J Biol Chem. 2017-1-6

[10]
MEF2 Transcription Factor Regulates Osteogenic Differentiation of Dental Pulp Stem Cells.

Cell Reprogram. 2016-8

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