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5-溴-3,4-二羟基苯甲醛通过激活真皮乳头细胞中的 Wnt/β-连环蛋白和自噬途径以及抑制 TGF-β 途径促进头发生长。

5-Bromo-3,4-dihydroxybenzaldehyde Promotes Hair Growth through Activation of Wnt/β-Catenin and Autophagy Pathways and Inhibition of TGF-β Pathways in Dermal Papilla Cells.

机构信息

Jeju Research Center for Natural Medicine, Jeju National University, Jeju 63243, Korea.

Department of Medicine, School of Medicine, Jeju National University, Jeju 63243, Korea.

出版信息

Molecules. 2022 Mar 28;27(7):2176. doi: 10.3390/molecules27072176.

DOI:10.3390/molecules27072176
PMID:35408575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9000556/
Abstract

Various studies addressing the increasing problem of hair loss, using natural products with few side effects, have been conducted. 5-bromo-3,4-dihydroxybenzaldehyde (BDB) exhibited anti-inflammatory effects in mouse models of atopic dermatitis and inhibited UVB-induced oxidative stress in keratinocytes. Here, we investigated its stimulating effect and the underlying mechanism of action on hair growth using rat vibrissa follicles and dermal papilla cells (DPCs), required for the regulation of hair cycle and length. BDB increased the length of hair fibers in rat vibrissa follicles and the proliferation of DPCs, along with causing changes in the levels of cell cycle-related proteins. We investigated whether BDB could trigger anagen-activating signaling pathways, such as the Wnt/β-catenin pathway and autophagy in DPCs. BDB induces activation of the Wnt/β-catenin pathway through the phosphorylation of GSG3β and β-catenin. BDB increased the levels of autophagic vacuoles and autophagy regulatory proteins Atg7, Atg5, Atg16L, and LC3B. We also investigated whether BDB inhibits the TGF-β pathway, which promotes transition to the catagen phase. BDB inhibited the phosphorylation of Smad2 induced by TGF-β1. Thus, BDB can promote hair growth by modulating anagen signaling by activating Wnt/β-catenin and autophagy pathways and inhibiting the TGF-β pathway in DPCs.

摘要

已经进行了各种研究,旨在解决日益严重的脱发问题,并使用副作用较少的天然产品。5-溴-3,4-二羟基苯甲醛(BDB)在特应性皮炎的小鼠模型中表现出抗炎作用,并抑制了角质形成细胞中 UVB 诱导的氧化应激。在这里,我们使用大鼠触须毛囊和真皮乳头细胞(DPC)研究了其对毛发生长的刺激作用及其潜在的作用机制,这是调节毛发生长周期和长度所必需的。BDB 增加了大鼠触须毛囊中纤维的长度和 DPC 的增殖,并导致细胞周期相关蛋白水平发生变化。我们研究了 BDB 是否可以触发 DPC 中的毛发生长激活信号通路,如 Wnt/β-catenin 通路和自噬。BDB 通过 GSG3β 和 β-catenin 的磷酸化诱导 Wnt/β-catenin 通路的激活。BDB 增加了自噬小体和自噬调节蛋白 Atg7、Atg5、Atg16L 和 LC3B 的水平。我们还研究了 BDB 是否抑制 TGF-β 通路,该通路促进向退行期的转变。BDB 抑制了 TGF-β1 诱导的 Smad2 磷酸化。因此,BDB 可以通过激活 Wnt/β-catenin 和自噬途径以及抑制 DPC 中的 TGF-β 途径来调节毛发生长信号,从而促进毛发生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d113/9000556/df02bb22f5ec/molecules-27-02176-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d113/9000556/6c0b1c183820/molecules-27-02176-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d113/9000556/f9ad580160ad/molecules-27-02176-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d113/9000556/37464000a16d/molecules-27-02176-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d113/9000556/df0d31025e1b/molecules-27-02176-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d113/9000556/df02bb22f5ec/molecules-27-02176-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d113/9000556/6c0b1c183820/molecules-27-02176-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d113/9000556/f9ad580160ad/molecules-27-02176-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d113/9000556/37464000a16d/molecules-27-02176-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d113/9000556/df0d31025e1b/molecules-27-02176-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d113/9000556/df02bb22f5ec/molecules-27-02176-g005a.jpg

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