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千里光乙醇提取物通过抑制 EGR-1 依赖的 MMP1 转录来抑制 HaCaT 角质形成细胞中的 MMP1 表达。

Inhibition of EGR-1-dependent MMP1 transcription by ethanol extract of Ageratum houstonianum in HaCaT keratinocytes.

机构信息

Department of Biological Sciences, Konkuk University, Seoul, 05029, Republic of Korea.

Cancer and Metabolism Institute, Konkuk University, Seoul, 05029, Republic of Korea.

出版信息

Mol Biol Rep. 2021 Jan;48(1):1-11. doi: 10.1007/s11033-020-06091-1. Epub 2021 Jan 15.

Abstract

Matrix metalloproteinase 1 (MMP-1) initiates the breakdown of matrix networks by cleaving fibrillar collagen during the pathophysiological progression of skin aging. Ageratum houstonianum ethanol extract (AHE) has been used as a traditional herbal medicine to treat external wounds and skin diseases. However, the mechanism of action underlying A. houstonianum-mediated modulation of skin aging has not been investigated. In this study, we evaluated the effect of AHE on MMP-1 expression in HaCaT keratinocytes. Gene expression was analyzed by Reverse transcription-PCR (RT-PCR), Quantitative real-time PCR (Q-PCR), gene promoter-reporter assay, and immunoblotting. We found that AHE abrogated TNFα-induced MMP1 expression at the transcriptional level via the suppression of ERK1/2 mitogen-activated protein kinase (MAPK)-mediated Early Growth Response 1 (EGR1) expression. We also demonstrated that β-caryophyllene, a cannabinoid receptor 2 (CB2) agonist, is a functional component of the AHE that inhibits TNFα-induced EGR-1 and MMP1 expression. AHE exerts inhibitory activity on TNFα-induced MMP1 expression at the transcription level through EGR-1 downregulation in keratinocytes. β-Caryophyllene is a bioactive ingredient of AHE that is responsible for the inhibition of TNFα-induced EGR1 expression. β-Caryophyllene can be used as a potential agent to prevent inflammation-induced skin aging.

摘要

基质金属蛋白酶 1(MMP-1)在皮肤衰老的病理生理过程中通过裂解纤维状胶原而启动基质网络的破坏。白花丹乙醇提取物(AHE)已被用作传统草药治疗外伤口和皮肤病。然而,A. houstonianum 介导的皮肤老化调节作用的机制尚未得到研究。在这项研究中,我们评估了 AHE 对 HaCaT 角质形成细胞中 MMP-1 表达的影响。通过逆转录-PCR(RT-PCR)、定量实时 PCR(Q-PCR)、基因启动子-报告基因测定和免疫印迹分析基因表达。我们发现 AHE 通过抑制 ERK1/2 丝裂原激活蛋白激酶(MAPK)介导的早期生长反应 1(EGR1)表达,在转录水平上消除了 TNFα 诱导的 MMP1 表达。我们还表明,大麻素受体 2(CB2)激动剂β-石竹烯是 AHE 的一种功能成分,可抑制 TNFα 诱导的 EGR-1 和 MMP1 表达。AHE 通过下调角质形成细胞中的 EGR-1 来抑制 TNFα 诱导的 MMP1 表达的转录活性。β-石竹烯是 AHE 的一种生物活性成分,可抑制 TNFα 诱导的 EGR1 表达。β-石竹烯可用作预防炎症诱导的皮肤衰老的潜在药物。

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