Hair growth-promoting effects of Enz_MoriL on human dermal papilla cells through modulation of the Wnt/β-Catenin and JAK-STAT signaling pathways

被引:2
|
作者
Chang, Boyoon [1 ]
Bae, Jinhye [1 ]
Lee, Dong-Sung [2 ]
Kim, Sungyeon [1 ]
机构
[1] Wonkwang Univ, Inst Pharmaceut Res & Dev, Coll Pharm, Iksan 54538, Jeollabuk Do, South Korea
[2] Chosun Univ, Coll Pharm, 309,Pilmun Daero, Gwangju 61452, South Korea
关键词
Enzyme treated Morus alba L. leaf; Enz_MoriL; Alopecia; Hair growth; Wnt pathway; JAK-STAT; 5-ALPHA-REDUCTASE; TOXICITY;
D O I
10.1007/s00403-024-02977-3
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Enz_MoriL is a naturally occurring substance extracted from the leaves of Morus alba L. through enzymatic conversion. Historically, M. alba L. has been recognized for its potential to promote hair regrowth. However, the precise mechanism by which Enz_MoriL affects human hair follicle dermal papilla cells (hDPCs) remains unclear. The aim of this study was to investigate the molecular basis of Enz_MoriL's effect on hair growth in hDPCs. Interferon-gamma (IFN-gamma) was used to examine the effects of Enz_MoriL on hDPCs during the anagen and catagen phases, as well as under conditions mimicking alopecia areata (AA). Enz_MoriL demonstrated the ability to promote cell proliferation in both anagen and catagen stages. It increased the levels of active beta-catenin in the catagen stage induced by IFN-gamma, leading to its nuclear translocation. This effect was achieved by increasing the phosphorylation of GSK3 beta and decreasing the expression of DKK-1. This stimulation induced proliferation in hDPCs and upregulated the expression of the Wnt family members 3a, 5a, and 7a at the transcript level. Additionally, Enz_MoriL suppressed JAK1 and STAT3 phosphorylation, contrasting with IFN-gamma, which induced them in the catagen stage. In conclusion, Enz_MoriL directly induced signals for anagen re-entry into hDPCs by affecting the Wnt/beta-catenin pathway and enhancing the production of growth factors. Furthermore, Enz_MoriL attenuated and reversed the interferon-induced AA-like environment by blocking the JAK-STAT pathway in hDPCs.
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页数:11
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