Research Papers:
Gsdma3 regulates hair follicle differentiation via Wnt5a-mediated non-canonical Wnt signaling pathway
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Abstract
Long He1, Mingxing Lei2,3, Yizhan Xing4, Yuhong Li4, Chunyan Hu4, Peixing Chen1, Xiaohua Lian4, Tian Yang4, Wanqian Liu1 and Li Yang1
1“111” Project Laboratory of Biomechanics and Tissue Repair & Key Laboratory of Biorheological Science and Technology of Ministry of Education, College of Bioengineering, Chongqing University, Chongqing 400044, China
2Integrative Stem Cell Center, China Medical University Hospital, China Medical University, Taichung 40402, Taiwan
3Institute of New Drug Development, College of Biopharmaceutical and Food Sciences, China Medical University, Taichung 40402, Taiwan
4Department of Cell Biology, Third Military Medical University, Chongqing 400038, China
Correspondence to:
Wanqian Liu, email: [email protected]
Li Yang, email: [email protected]
Mingxing Lei, email: [email protected]
Keywords: non-canonical Wnt signaling pathway; Gsdma3, hair follicle; epithelial-mesenchymal interaction; differentiation
Received: July 18, 2017 Accepted: September 21, 2017 Published: October 31, 2017
ABSTRACT
Hair follicle is a mini-organ that consists of complex but well-organized structures, which are differentiated from hair follicle progenitor or stem cells. How non-canonical Wnt signaling pathway is involved in regulating hair follicle differentiation remains elusive. Here we showed that Wnt5a regulates hair follicle differentiation through an epithelial-mesenchymal interaction mechanism in mice. We first observed that Wnt5a is expressed in the epithelial and dermal papilla cells during hair follicle development and growth. For the upstream of Wnt5a, RT-PCR and immunohistochemistry staining showed that Wnt5a expression is significantly decreased in the Gsdma3-mutant mice in vivo. Overexpression of Gsdma3 results in a significantly increased expression of Wnt5a in the cultured epidermal cells in vitro. We also checked the downstream factors of Wnt5a by adenovirus-mediated overexpression of Wnt5a to the dermal papilla cells isolated from the mouse whisker. We found that overexpression of Wnt5a suppresses canonical Wnt signaling pathway effectors such as β-catenin and Lef1. In addition, genes involved in maintaining cell quiescent state are also significantly decreased in their expression to the DP cells which were treated by Wnt5a. Our study indicates that Wnt5a mediates epithelia-expressed Gsdma3 to influence DP cell behaviors, which in turn regulate hair follicle epithelia differentiation in mice.
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