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螨虫和蟑螂蛋白酶可激活人肺上皮细胞中的p44/p42丝裂原活化蛋白激酶。

Mite and cockroach proteases activate p44/p42 MAP kinases in human lung epithelial cells.

作者信息

Kuderer Nicole M, San-Juan-Vergara Homero G, Kong Xiaoyuan, Esch Robert, Lockey Richard F, Mohapatra Shyam S

机构信息

Joy McCann Culverhouse Airway Disease Center, University of South Florida and James A Haley VA Hospital, Tampa, FL, USA.

出版信息

Clin Mol Allergy. 2003 Oct 30;1(1):1. doi: 10.1186/1476-7961-1-1.

Abstract

BACKGROUND

The mechanisms underlying epithelial cell activation by indoor inhaled antigens are poorly understood. METHODS: In this study, we investigated the role of mitogen-activated protein kinases (MAPKs) in A549 epithelial cells upon exposure to antigens of house dust mite (HDMA), German cockroach (GCA), and American cockroach (ACA). RESULTS: Each of these antigens induced a significant increase in IL-8 levels compared to the medium control. Exposure of A549 cells to these antigens induced the phosphorylation of p44/42 MAPKs within 5 minutes, which reached a peak at 25 minutes later and reached baseline levels at 1 hour after exposure. PD98059, a MEK1 inhibitor, significantly decreased phosphorylation of p44/p42 MAPKs and IL-8 production. Exposure of A549 cells with antigens, which had been preincubated with different protease inhibitors, also resulted in a reduction of both MAPK phosphorylation and IL-8 production. CONCLUSION: Thus, proteolytic antigens present in HDMA, GCA and ACA activate the p44/42 MAPKs airway epithelial cells, which lead to elevated IL-8 production and initiation of the inflammatory cascade.

摘要

背景

室内吸入性抗原激活上皮细胞的机制尚不清楚。

方法

在本研究中,我们调查了丝裂原活化蛋白激酶(MAPKs)在A549上皮细胞暴露于屋尘螨(HDMA)、德国小蠊(GCA)和美洲大蠊(ACA)抗原时所起的作用。

结果

与培养基对照相比,这些抗原中的每一种都能显著提高白细胞介素-8(IL-8)水平。A549细胞暴露于这些抗原后5分钟内诱导p44/42 MAPKs磷酸化,25分钟后达到峰值,暴露后1小时恢复到基线水平。MEK1抑制剂PD98059显著降低p44/p42 MAPKs的磷酸化和IL-8的产生。用不同蛋白酶抑制剂预孵育过的抗原处理A549细胞,也会导致MAPK磷酸化和IL-8产生减少。

结论

因此,HDMA、GCA和ACA中存在的蛋白水解抗原激活气道上皮细胞中的p44/42 MAPKs,导致IL-8产生增加并引发炎症级联反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8e6/312598/0677bdea0f07/1476-7961-1-1-1.jpg

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