首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >Aster glehni Extract Containing Caffeoylquinic Compounds Protects Human Keratinocytes through the TRPV4-PPARδ-AMPK Pathway
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Aster glehni Extract Containing Caffeoylquinic Compounds Protects Human Keratinocytes through the TRPV4-PPARδ-AMPK Pathway

机译:含有咖啡酰奎宁化合物的紫苑提取物通过TRPV4-PPARδ-AMPK途径保护人类角质形成细胞

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摘要

Aster glehni (AG) has been used in cooking and as a medicine to treat various diseases for over hundreds of years in Korea. To speculate the protective effects of AG on skin barrier, we estimated the protein levels of biomarkers related to skin barrier protection in human keratinocytes, HaCaT cells treated with sodium dodecyl sulfate (SDS), or 2,4-dinitrochlorobenzene (DNCB). The protein levels for keratin, involucrin, defensin, tumor necrosis factor alpha (TNFα), peroxisome proliferator-activated receptor delta (PPARδ), 5′ adenosine monophosphate-activated protein kinase (AMPK), serine palmitoyltransferase long chain base subunit 2 (SPTLC2), and transient receptor potential cation channel subfamily V member 4 (TRPV4) were evaluated using western blotting or immunocytochemistry in HaCaT cells. AG extract increased the protein levels of PPARδ, phosphorylated AMPK, SPTLC2, keratin, involucrin, and defensin compared to the SDS or DNCB control group. However, TNFα expression increased by SDS or DNCB was decreased with AG extract. The order of action of each regulatory biomarker in AG pathway was identified TRPV4→PPARδ→AMPK from antagonist and siRNA treatment studies. AG can ameliorate the injury of keratinocytes caused by SDS or DNCB through the sequential regulation of TRPV4→PPARδ→AMPK pathway.
机译:Aster glehni(AG)在韩国已被用于烹饪以及作为治疗多种疾病的药物。为了推测AG对皮肤屏障的保护作用,我们估计了人类角质形成细胞,十二烷基硫酸钠(SDS)或2,4-二硝基氯苯(DNCB)处理的HaCaT细胞中与皮肤屏障保护相关的生物标志物的蛋白质水平。角蛋白,整合素,防御素,肿瘤坏死因子α(TNFα),过氧化物酶体增殖物激活受体δ(PPARδ),5'腺苷单磷酸激活蛋白激酶(AMPK),丝氨酸棕榈酰转移酶长链碱基亚基2(SPTLC2)的蛋白水平,并使用Western印迹或免疫细胞化学在HaCaT细胞中评估了瞬时受体电位阳离子通道亚家族V成员4(TRPV4)。与SDS或DNCB对照组相比,AG提取物可提高PPARδ,磷酸化的AMPK,SPTLC2,角蛋白,囊蛋白和防御素的蛋白质水平。然而,SDS或DNCB增加的TNFα表达被AG提取物降低。通过拮抗剂和siRNA治疗研究确定了TRPV4→PPARδ→AMPK在AG途径中每种调节性生物标志物的作用顺序。 AG可以通过依次调节TRPV4→PPARδ→AMPK途径来减轻SDS或DNCB对角质形成细胞的损伤。

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