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去甲加兰他敏通过生长期激活信号通路刺激毛乳头细胞增殖。

Norgalanthamine Stimulates Proliferation of Dermal Papilla Cells via Anagen-Activating Signaling Pathways.

作者信息

Yoon Hoon-Seok, Kang Jung-Il, Kim Sung Min, Ko Ara, Koh Young-Sang, Hyun Jin-Won, Yoon Sang-Pil, Ahn Mee Jung, Kim Young Ho, Kang Ji-Hoon, Yoo Eun-Sook, Kang Hee-Kyoung

机构信息

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

Jeju Research Center for Natural Medicine, Jeju National University.

出版信息

Biol Pharm Bull. 2019;42(1):139-143. doi: 10.1248/bpb.b18-00226.

DOI:10.1248/bpb.b18-00226
PMID:30606985
Abstract

Norgalanthamine has been shown to possess hair-growth promoting effects, including increase in hair-fiber length in cultured rat vibrissa follicles and increase in dermal papilla cell (DPC) proliferation. However, the intracellular mechanisms that underlie the action of norgalanthamine in DPCs have not been investigated. In this study, we addressed the ability of norgalanthamine to trigger anagen-activating signaling pathways in DPCs. Norgalanthamine significantly increased extracellular signal-regulated kinase (ERK) 1/2 phosphorylation at 0.1 µM, a concentration at which DPC proliferation was also induced. Furthermore, the increases in norgalanthamine-induced ERK 1/2 activation and subsequent DPC proliferation were suppressed by the mitogen-activated protein kinase/ERK kinase (MEK) 1/2 inhibitor, U0126. A 0.1 µM dose of norgalanthamine also increased phosphorylation of AKT, which was followed by an increase in glycogen synthase kinase 3β phosphorylation and nuclear translocation of β-catenin. In addition, LY294002, a phosphatidylinositol 3 kinase (PI3K) inhibitor, blocked the effect of norgalanthamine on DPC proliferation. These results suggest that norgalanthamine can stimulate the anagen phase of the hair cycle in DPCs via activation of the ERK 1/2, PI3K/AKT, and Wnt/β-catenin pathways.

摘要

去甲加兰他敏已被证明具有促进头发生长的作用,包括增加培养的大鼠触须毛囊中的毛纤维长度以及增加真皮乳头细胞(DPC)的增殖。然而,去甲加兰他敏在DPCs中发挥作用的细胞内机制尚未得到研究。在本研究中,我们探讨了去甲加兰他敏触发DPCs中毛发生长期激活信号通路的能力。去甲加兰他敏在0.1µM时显著增加细胞外信号调节激酶(ERK)1/2的磷酸化,该浓度也能诱导DPC增殖。此外,丝裂原活化蛋白激酶/ERK激酶(MEK)1/2抑制剂U0126抑制了去甲加兰他敏诱导的ERK 1/2激活增加以及随后的DPC增殖。0.1µM剂量的去甲加兰他敏也增加了AKT的磷酸化,随后糖原合酶激酶3β磷酸化增加以及β-连环蛋白的核转位。此外,磷脂酰肌醇3激酶(PI3K)抑制剂LY294002阻断了去甲加兰他敏对DPC增殖的影响。这些结果表明,去甲加兰他敏可通过激活ERK 1/2、PI3K/AKT和Wnt/β-连环蛋白通路刺激DPCs中毛发周期的生长期。

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