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8-氧鸟嘌呤-DNA 糖基化酶 1 缺乏通过调节细胞和小鼠中的 STAT6 和 IL-4 来改变过敏性气道炎症。

8-Oxoguanine-DNA glycosylase 1 deficiency modifies allergic airway inflammation by regulating STAT6 and IL-4 in cells and in mice.

机构信息

Department of Biochemistry and Molecular Biology, University of North Dakota, Grand Forks, ND 58203-9037, USA.

出版信息

Free Radic Biol Med. 2012 Jan 15;52(2):392-401. doi: 10.1016/j.freeradbiomed.2011.10.490. Epub 2011 Nov 3.

Abstract

8-Oxoguanine-DNA glycosylase (OGG-1) is a base excision DNA repair enzyme; however, its function in modulating allergic diseases remains undefined. Using OGG-1 knockout (KO) mice, we show that this protein affects allergic airway inflammation after sensitization and challenge by ovalbumin(OVA). OGG-1 KO mice exhibited less inflammatory cell infiltration and reduced oxidative stress in the lungs after OVA challenge compared to WT mice. The KO phenotype included decreased IL-4, IL-6, IL-10, and IL-17 in lung tissues. In addition, OGG-1 KO mice showed decreased expression and phosphorylation of STAT6 as well as NF-κB. Down-regulation of OGG-1 by siRNA lowered ROS and IL-4 levels but increased IFN-γ production in cultured epithelial cells after exposure to house dust mite extracts. OGG-1 may affect the levels of oxidative stress and proinflammatory cytokines during asthmatic conditions. OGG-1 deficiency negatively regulates allergen-induced airway inflammatory response.

摘要

8-氧鸟嘌呤-DNA 糖基化酶(OGG-1)是一种碱基切除 DNA 修复酶;然而,其在调节过敏疾病中的作用尚未确定。使用 OGG-1 敲除(KO)小鼠,我们表明该蛋白在卵清蛋白(OVA)致敏和攻击后影响过敏性气道炎症。与 WT 小鼠相比,OGG-1 KO 小鼠在 OVA 攻击后肺部的炎症细胞浸润和氧化应激减少。KO 表型包括肺组织中 IL-4、IL-6、IL-10 和 IL-17 的减少。此外,OGG-1 KO 小鼠表现出 STAT6 和 NF-κB 的表达和磷酸化减少。用 siRNA 下调 OGG-1 可降低暴露于屋尘螨提取物后培养的上皮细胞中的 ROS 和 IL-4 水平,但增加 IFN-γ 的产生。在哮喘情况下,OGG-1 可能会影响氧化应激和促炎细胞因子的水平。OGG-1 缺乏负调节变应原诱导的气道炎症反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/740a/3740570/52b17ad1adeb/nihms336506f1.jpg

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