Institute of Pharmaceutical Research and Development, College of Pharmacy, Wonkwang University, Iksan, Jeonbuk, 54538, Republic of Korea.
College of Pharmacy, Chosun University, 309, Pilmun-daero, Dong-gu, Gwangju, 61452, Republic of Korea.
Arch Dermatol Res. 2024 May 29;316(6):290. doi: 10.1007/s00403-024-02977-3.
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-γ) 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 β-catenin in the catagen stage induced by IFN-γ, leading to its nuclear translocation. This effect was achieved by increasing the phosphorylation of GSK3β 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-γ, which induced them in the catagen stage. In conclusion, Enz_MoriL directly induced signals for anagen re-entry into hDPCs by affecting the Wnt/β-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.
Enz_MoriL 是一种从桑科植物桑的叶子中通过酶转化提取的天然物质。历史上,桑被认为具有促进头发生长的潜力。然而,Enz_MoriL 影响人类毛囊真皮乳头细胞 (hDPC) 的具体机制尚不清楚。本研究旨在探讨 Enz_MoriL 对 hDPC 中毛发生长的分子基础。干扰素-γ (IFN-γ) 用于研究 Enz_MoriL 在 hDPC 处于生长期和退行期以及模拟斑秃 (AA) 条件下对 hDPC 的影响。Enz_MoriL 表现出在生长期和退行期促进细胞增殖的能力。它增加了 IFN-γ诱导的退行期中活性 β-连环蛋白的水平,导致其核转位。这一效应是通过增加 GSK3β 的磷酸化和降低 DKK-1 的表达来实现的。这种刺激诱导 hDPC 增殖,并在上调 Wnt 家族成员 3a、5a 和 7a 的转录水平表达。此外,Enz_MoriL 抑制了 JAK1 和 STAT3 的磷酸化,与 IFN-γ 诱导的作用相反,后者在退行期诱导了它们的磷酸化。总之,Enz_MoriL 通过影响 Wnt/β-连环蛋白通路和增强生长因子的产生,直接诱导 hDPC 进入生长期。此外,Enz_MoriL 通过阻断 hDPC 中的 JAK-STAT 通路,减弱并逆转了干扰素诱导的 AA 样环境。