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蛋白酶激活受体-2缺陷小鼠的屋尘螨诱发过敏性肺部炎症减轻。

Protease-activated receptor-2 deficient mice have reduced house dust mite-evoked allergic lung inflammation.

作者信息

de Boer J Daan, Van't Veer Cornelis, Stroo Ingrid, van der Meer Anne J, de Vos Alex F, van der Zee Jaring S, Roelofs Joris J T H, van der Poll Tom

机构信息

Academic Medical Center, University of Amsterdam, Center of Infection and Immunity Amsterdam & Center for Experimental and Molecular Medicine, Amsterdam, the Netherlands

Academic Medical Center, University of Amsterdam, Center of Infection and Immunity Amsterdam & Center for Experimental and Molecular Medicine, Amsterdam, the Netherlands.

出版信息

Innate Immun. 2014 Aug;20(6):618-25. doi: 10.1177/1753425913503387. Epub 2013 Sep 18.

Abstract

Protease-activated receptor-2 (PAR2) is abundantly expressed in the pulmonary compartment. House dust mite (HDM) is a common cause of allergic asthma and contains multiple PAR2 agonistic proteases. The aim of this study was to determine the role of PAR2 in HDM-induced allergic lung inflammation. For this, the extent of allergic lung inflammation was studied in wild type (Wt) and PAR2 knockout (KO) mice after repeated airway exposure to HDM. HDM exposure of Wt mice resulted in a profound influx of eosinophils in bronchoalveolar lavage fluid (BALF) and accumulation of eosinophils in lung tissue, which both were strongly reduced in PAR2 KO mice. PAR2 KO mice demonstrated attenuated lung pathology and protein leak in the bronchoalveolar space, accompanied by lower BALF levels of the anaphylatoxins C3a and C5a. This study reveals, for the first time, an important role for PAR2 in allergic lung inflammation induced by the clinically relevant allergens contained in HDM.

摘要

蛋白酶激活受体-2(PAR2)在肺组织中大量表达。屋尘螨(HDM)是过敏性哮喘的常见诱因,且含有多种PAR2激动性蛋白酶。本研究旨在确定PAR2在HDM诱导的过敏性肺部炎症中的作用。为此,在野生型(Wt)和PAR2基因敲除(KO)小鼠反复气道暴露于HDM后,研究过敏性肺部炎症的程度。Wt小鼠暴露于HDM后,支气管肺泡灌洗液(BALF)中嗜酸性粒细胞大量涌入,肺组织中嗜酸性粒细胞积聚,而在PAR2 KO小鼠中这两种情况均明显减少。PAR2 KO小鼠表现出肺部病理变化减轻以及支气管肺泡空间内蛋白质渗漏减少,同时BALF中过敏毒素C3a和C5a的水平较低。本研究首次揭示了PAR2在由HDM中所含临床相关过敏原诱导的过敏性肺部炎症中的重要作用。

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