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白癜风皮肤活检样本和外周血单个核细胞中与黑素细胞功能调节相关的细胞因子的 mRNA 表达谱。

The mRNA expression profile of cytokines connected to the regulation of melanocyte functioning in vitiligo skin biopsy samples and peripheral blood mononuclear cells.

机构信息

Department of Physiology, University of Tartu, Tartu, Estonia.

出版信息

Hum Immunol. 2012 Apr;73(4):393-8. doi: 10.1016/j.humimm.2012.01.011. Epub 2012 Jan 31.

Abstract

The expression pattern of several genes associated with different processes in melanocytes, including melanogenesis, is changed in vitiligo patients. We evaluated possible changes in the expression of interleukin (IL)-10 family cytokines (IL26, IL-28A, IL28B, IL29), their receptor subunits (IL20RB, IL22RA2, IL28RA), and genes potentially related to functioning of melanocytes (MDM1, IFNA1, IFNB1, IFNG, and ICAM1) in the case of vitiligo. We observed mRNA expression in vitiligo patients' and controls' skin and peripheral blood mononuclear cells using quantitative real-time polymerase chain reaction. The mRNA expression pattern of IL20RB, IL22RA2, IL-28A, IL28B, IL28RA, MDM1, IFNA1, IFNB1, IFNG, and ICAM1 changed in vitiligo skin and/or peripheral blood mononuclear cells (PBMC) compared with controls. All of these genes may potentially be involved in vitiligo pathogenesis through controlling or participating in different pathways that regulate survival/apoptosis, development and migration of melanocytes, and melanogenesis. This study presents additional support for our previous findings about the importance of IL-10 family cytokines in vitiligo, in particular the possible involvement of IL-22. Further studies should be considered.

摘要

在白癜风患者中,与黑素细胞中不同过程相关的几个基因的表达模式发生改变。我们评估了白癜风患者皮肤和外周血单个核细胞中白细胞介素 (IL)-10 家族细胞因子 (IL26、IL-28A、IL28B、IL29)、其受体亚基 (IL20RB、IL22RA2、IL28RA) 以及与黑素细胞功能相关的潜在基因 (MDM1、IFNA1、IFNB1、IFNG 和 ICAM1) 的表达可能发生的变化。我们使用定量实时聚合酶链反应在白癜风患者和对照组的皮肤和外周血单个核细胞中观察了 mRNA 的表达。与对照组相比,白癜风皮肤和/或外周血单个核细胞中 IL20RB、IL22RA2、IL-28A、IL28B、IL28RA、MDM1、IFNA1、IFNB1、IFNG 和 ICAM1 的 mRNA 表达模式发生了改变。所有这些基因都可能通过控制或参与调节黑素细胞存活/凋亡、发育和迁移以及黑色素生成的不同途径,潜在参与白癜风的发病机制。本研究为我们之前关于白细胞介素-10 家族细胞因子在白癜风中的重要性的发现提供了更多支持,特别是 IL-22 可能的参与。应该考虑进一步的研究。

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