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使用荧光磷蛋白染料来表征暴露于柴油尾气颗粒化学物质的巨噬细胞和上皮细胞培养物中氧化应激诱导的信号通路成分。

Use of a fluorescent phosphoprotein dye to characterize oxidative stress-induced signaling pathway components in macrophage and epithelial cultures exposed to diesel exhaust particle chemicals.

作者信息

Wang Meiying, Xiao Gary Guishan, Li Ning, Xie Yongming, Loo Joseph A, Nel Andre E

机构信息

Department of Medicine, Division of Clinical Immunology and Allergy, and David Geffen School of Medicine, University of California Los Angeles, CA 90095, USA.

出版信息

Electrophoresis. 2005 Jun;26(11):2092-108. doi: 10.1002/elps.200410428.

Abstract

A large body of evidence has shown that exposure to ambient particulate matter (PM) leads to asthma exacerbation through an excitation of allergic inflammation. Utilizing diesel exhaust particles (DEPs) as a model air pollutant, we and others have demonstrated that PM contains redox-active chemicals that generate inflammation through an oxidative stress mechanism. Recently, the strengths of proteomics have enabled us to demonstrate that organic DEP extracts induce a hierarchical expression pattern of oxidative stress-induced proteins in macrophages and epithelial cells. As a further extension of this work, we now employ a new phosphosensor fluorescent dye, Pro-Q Diamond, to elucidate the induction of phosphoproteins and intracellular signaling cascades that may play a role in DEP-induced inflammation. We demonstrate that DEPs induced the phosphorylation of several phosphoproteins that belong to a number of signaling pathways as well as other oxidative stress pathways. In combination with cytokine array, phosphoproteome analysis using Pro-Q Diamond allowed us to characterize the aromatic and polar chemicals of DEPs that are involved in the activation of three different mitogen-activated protein (MAP) kinase signaling pathways.

摘要

大量证据表明,暴露于环境颗粒物(PM)会通过激发过敏性炎症导致哮喘加重。我们和其他人利用柴油尾气颗粒(DEP)作为模型空气污染物,证明了PM含有通过氧化应激机制引发炎症的氧化还原活性化学物质。最近,蛋白质组学的优势使我们能够证明有机DEP提取物在巨噬细胞和上皮细胞中诱导氧化应激诱导蛋白的分级表达模式。作为这项工作的进一步延伸,我们现在使用一种新的磷传感器荧光染料Pro-Q Diamond,来阐明可能在DEP诱导的炎症中起作用的磷蛋白的诱导和细胞内信号级联反应。我们证明DEP诱导了属于多个信号通路以及其他氧化应激通路的几种磷蛋白的磷酸化。结合细胞因子阵列,使用Pro-Q Diamond进行的磷酸蛋白质组分析使我们能够表征DEP中参与激活三种不同丝裂原活化蛋白(MAP)激酶信号通路的芳香族和极性化学物质。

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