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甘露糖赤藓糖醇脂通过抑制培养的人角质形成细胞中c-Jun氨基末端激酶磷酸化,改善紫外线A诱导的水通道蛋白-3下调。

Mannosylerythritol lipids ameliorate ultraviolet A-induced aquaporin-3 downregulation by suppressing c-Jun N-terminal kinase phosphorylation in cultured human keratinocytes.

作者信息

Bae Il-Hong, Lee Sung Hoon, Oh Soojung, Choi Hyeongwon, Marinho Paulo A, Yoo Jae Won, Ko Jae Young, Lee Eun-Soo, Lee Tae Ryong, Lee Chang Seok, Kim Dae-Yong

机构信息

R&D Center, Amorepacific Corporation, Yongin 17074, Korea.

Department of Veterinary Pathology, College of Veterinary Medicine, Seoul National University, Seoul 08826, Korea.

出版信息

Korean J Physiol Pharmacol. 2019 Mar;23(2):113-120. doi: 10.4196/kjpp.2019.23.2.113. Epub 2019 Feb 15.

Abstract

Mannosylerythritol lipids (MELs) are glycolipids and have several pharmacological efficacies. MELs also show skin-moisturizing efficacy through a yet-unknown underlying mechanism. Aquaporin-3 (AQP3) is a membrane protein that contributes to the water homeostasis of the epidermis, and decreased AQP3 expression following ultraviolet (UV)-irradiation of the skin is associated with reduced skin moisture. No previous study has examined whether the skin-moisturizing effect of MELs might act through the modulation of AQP3 expression. Here, we report for the first time that MELs ameliorate the UVA-induced downregulation of AQP3 in cultured human epidermal keratinocytes (HaCaT keratinocytes). Our results revealed that UVA irradiation decreases AQP3 expression at the protein and messenger RNA (mRNA) levels, but that MEL treatment significantly ameliorated these effects. Our mitogen-activated protein kinase inhibitor analysis revealed that phosphorylation of c-Jun N-terminal kinase (JNK), but not extracellular signal-regulated kinase or p38, mediates UVA-induced AQP3 downregulation, and that MEL treatment significantly suppressed the UVA-induced phosphorylation of JNK. To explore a possible mechanism, we tested whether MELs could regulate the expression of peroxidase proliferator-activated receptor gamma (PPAR-γ), which acts as a potent transcription factor for AQP3 expression. Interestingly, UVA irradiation significantly inhibited the mRNA expression of PPAR-γ in HaCaT keratinocytes, whereas a JNK inhibitor and MELs significantly rescued this effect. Taken together, these findings suggest that MELs ameliorate UVA-induced AQP3 downregulation in HaCaT keratinocytes by suppressing JNK activation to block the decrease of PPAR-γ. Collectively, our findings suggest that MELs can be used as a potential ingredient that modulates AQP3 expression to improve skin moisturization following UVA irradiation-induced damage.

摘要

甘露糖赤藓糖醇脂(MELs)是糖脂,具有多种药理功效。MELs还通过一种尚不清楚的潜在机制展现出皮肤保湿功效。水通道蛋白3(AQP3)是一种膜蛋白,对表皮的水平衡有作用,皮肤紫外线(UV)照射后AQP3表达降低与皮肤水分减少有关。此前尚无研究探讨MELs的皮肤保湿作用是否可能通过调节AQP3表达来实现。在此,我们首次报道MELs可改善UVA诱导的人表皮角质形成细胞(HaCaT角质形成细胞)中AQP3的下调。我们的结果显示,UVA照射会降低蛋白和信使核糖核酸(mRNA)水平的AQP3表达,但MEL处理可显著改善这些影响。我们的丝裂原活化蛋白激酶抑制剂分析显示,c-Jun氨基末端激酶(JNK)的磷酸化介导了UVA诱导的AQP3下调,而非细胞外信号调节激酶或p38,且MEL处理显著抑制了UVA诱导的JNK磷酸化。为探究可能的机制,我们测试了MELs是否能调节过氧化物酶增殖物激活受体γ(PPAR-γ)的表达,PPAR-γ是AQP3表达的一种强效转录因子。有趣的是,UVA照射显著抑制了HaCaT角质形成细胞中PPAR-γ的mRNA表达,而JNK抑制剂和MELs可显著挽救这一效应。综上所述,这些发现表明MELs通过抑制JNK激活以阻止PPAR-γ的减少,从而改善UVA诱导的HaCaT角质形成细胞中AQP3的下调。总体而言,我们的发现表明MELs可作为一种潜在成分,调节AQP3表达以改善UVA照射诱导损伤后的皮肤保湿。

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