Literature DB >> 31152005

Pharmacological Activation of Thermo-Transient Receptor Potential Vanilloid 3 Channels Inhibits Hair Growth by Inducing Cell Death of Hair Follicle Outer Root Sheath.

Kangjiao Yan1, Xiaoying Sun1, Gongxin Wang1, Yani Liu1, KeWei Wang2.   

Abstract

Hair growth starts from hair follicles that reside in dermis, and abnormal hair growth is an early sign of hair follicle disease or systemic illness such as alopecia or hair loss. Therefore, identifying a target critical for dysfunctional hair follicles is fundamental to alleviating dermatologic or systemic diseases with hair abnormalities. The warm temperature-activated Ca2+-permeable transient receptor potential vanilloid 3 (TRPV3) channel protein is abundantly expressed in the skin keratinocytes, and dysfunctional TRPV3 causes human congenital Olmsted syndrome, characterized by skin diseases and alopecia, indicating an important role for TRPV3 in hair follicle development and hair growth. To validate TRPV3 as a therapeutic target, we investigated the impact of pharmacological modulation of TRPV3 on hair growth using a combination of biochemical and cell biology, immunohistochemical, whole-cell patch clamp, RNA interference, and pharmacological approaches. We found that functional TRPV3 channel proteins are highly expressed in hair follicle outer root sheath (ORS) cells as detected by Western blot analysis, immunohistochemical staining, and electrophysiological techniques. Pharmacological activation of TRPV3 by agonist natural carvacrol induces cell death of ORS cells, and topical application of carvacrol to mouse dorsal skin also inhibits hair growth. Conversely, specific inhibition of TRPV3 by inhibitor natural forsythoside B and short-hairpin RNA reverses the cell death induced by carvacrol-mediated TRPV3 activation in human ORS cells. Furthermore, forsythoside B results in a significant reversal of hair growth inhibition induced by agonist carvacrol. Altogether, our findings demonstrate that TRPV3 channel is critical for regulation of hair growth, and inhibition of TRPV3 may represent a promising therapy for hair loss or hair follicle-related skin diseases.
Copyright © 2019 by The American Society for Pharmacology and Experimental Therapeutics.

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Year:  2019        PMID: 31152005     DOI: 10.1124/jpet.119.258087

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  3 in total

1.  Mechanisms of proton inhibition and sensitization of the cation channel TRPV3.

Authors:  Haiyuan Wang; Pu Yang; Yungang Lu; Jin Wang; Jaepyo Jeon; Qiaochu Wang; Jin-Bin Tian; Bin Zang; Ye Yu; Michael X Zhu
Journal:  J Gen Physiol       Date:  2021-02-01       Impact factor: 4.086

2.  Preparation and optimization of aloe ferox gel loaded with Finasteride-Oregano oil nanocubosomes for treatment of alopecia.

Authors:  Khaled M Hosny; Waleed Y Rizg; Eman Alfayez; Samar S Elgebaly; Abdulmohsin J Alamoudi; Raed I Felimban; Hossam H Tayeb; Rayan Y Mushtaq; Awaji Y Safhi; Majed Alharbi; Alshaimaa M Almehmady
Journal:  Drug Deliv       Date:  2022-12       Impact factor: 6.419

3.  TRPV3 enhances skin keratinocyte proliferation through EGFR-dependent signaling pathways.

Authors:  Yujing Wang; Hang Li; Chu Xue; Hao Chen; Yanning Xue; Fang Zhao; Michael X Zhu; Zhengyu Cao
Journal:  Cell Biol Toxicol       Date:  2020-06-13       Impact factor: 6.691

  3 in total

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