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他卡西醇对 IFN-γ 诱导的永生化人表皮角质形成细胞角质蛋白 17 表达的影响。

Effect of Calcipotriol on IFN-γ-Induced Keratin 17 Expression in Immortalized Human Epidermal Keratinocyte Cells.

机构信息

Department of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China (mainland).

出版信息

Med Sci Monit. 2017 Dec 22;23:6049-6056. doi: 10.12659/msm.904850.

Abstract

BACKGROUND Calcipotriol ointment has been demonstrated to be a very safe and effective topical drug for psoriasis. This study aims to investigate the effect of calcipotriol on IFN-γ-induced keratin 17 (K17) expression in a human keratinocyte cell line (HaCaT), which is a widely accepted as a mimic in vitro model for psoriasis. MATERIAL AND METHODS We used Western blot, immunofluorescence staining, and luciferase reporter system assays to evaluate the expression of K17 and the possible underlying mechanisms. RESULTS Administration of IFN-γ (125-1000 U) increased K17 expression in a dose-dependent manner, and 250 U/ml IFN-γ significantly elevated K17 expression. The experimental results showed that calcipotriol at concentrations of 10^-7 M and 10^-5 M suppressed the IFN-γ-induced K17 expression by 58.10% and 70.68%, respectively. Through immunofluorescence staining and luciferase reporter assay, we found that Vitamin D Response Element (VDRE) affected IFN-activated site (Gamma-activated sequence, GAS) function at the transcriptional level and was involved in the inhibition of K17 expression. CONCLUSIONS Our data suggest that calcipotriol downregulates IFN-γ-mediated K17 expression in keratinocytes in a dose-dependent manner via VDRE effect GAS function. The inhibitory effect of calcipotriol on K17 expression may be a potential mechanism and function in the treatment psoriasis.

摘要

背景

卡泊三醇软膏已被证明是治疗银屑病非常安全有效的局部药物。本研究旨在探讨卡泊三醇对人角质形成细胞系(HaCaT)中 IFN-γ诱导的角蛋白 17(K17)表达的影响,HaCaT 被广泛认为是银屑病体外模型的模拟物。

材料和方法

我们使用 Western blot、免疫荧光染色和荧光素酶报告系统实验来评估 K17 的表达及其潜在的机制。

结果

IFN-γ(125-1000 U)给药以剂量依赖性方式增加 K17 的表达,250 U/ml IFN-γ可显著增加 K17 的表达。实验结果表明,卡泊三醇在 10^-7 M 和 10^-5 M 浓度下分别抑制 IFN-γ诱导的 K17 表达 58.10%和 70.68%。通过免疫荧光染色和荧光素酶报告实验,我们发现维生素 D 反应元件(VDRE)在转录水平上影响 IFN 激活位点(Gamma-activated sequence,GAS)的功能,并参与 K17 表达的抑制。

结论

我们的数据表明,卡泊三醇通过 VDRE 效应 GAS 功能,以剂量依赖性方式下调角质形成细胞中 IFN-γ介导的 K17 表达。卡泊三醇对 K17 表达的抑制作用可能是治疗银屑病的一种潜在机制和功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94f/5747147/2c5036e26f8d/medscimonit-23-6049-g001.jpg

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