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Quantitative proteomic changes in LPS-activated monocyte-derived dendritic cells: A SWATH-MS study

机译:LPS激活的单核细胞衍生树突状细胞的蛋白质组学定量变化:SWATH-MS研究

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摘要

Dendritic cells are key immune cells that respond to pathogens and co-ordinate many innate and adaptive immune responses. Quantitative mass spectrometry using Sequential Window Acquisition of all THeoretical fragment-ion spectra-Mass Spectrometry (SWATH-MS) was performed here to determine the global alterations in monocyte-derived dendritic cells (moDCs) in response to stimulation with lipopolysaccharide (LPS). A moDC library of 4,666 proteins was generated and proteins were quantified at 0, 6 and 24 h post-LPS stimulation using SWATH-MS. At 6 h and 24 h post-LPS exposure, the relative abundance of 227 and 282 proteins was statistically significantly altered (p-value ≤ 0.05), respectively. Functional annotation of proteins exhibiting significant changes in expression between the various time points led to the identification of clusters of proteins implicated in distinct cellular processes including interferon and interleukin signalling, endocytosis, the ER-phagosome pathway and antigen-presentation. In SWATH-MS major histocompatibility complex (MHC) class I proteins were highly upregulated at 24 h, whilst MHC class II proteins exhibited comparatively fewer changes over this period. This study provides new detailed insight into the global proteomic changes that occur in moDCs during antigen processing and presentation and further demonstrates the potential of SWATH-MS for the quantitative study of proteins involved in cellular processes.
机译:树突状细胞是对病原体作出反应并协调许多先天和适应性免疫反应的关键免疫细胞。使用顺序窗口定量质谱分析所有理论碎片离子光谱-质谱(SWATH-MS)在此进行,以确定响应于脂多糖(LPS)刺激的单核细胞衍生树突状细胞(moDCs)的整体变化。产生了4,666种蛋白质的moDC文库,并使用SWATH-MS在LPS刺激后0、6和24 h对蛋白质进行了定量。在LPS暴露后6小时和24小时时,分别有227和282个蛋白质的相对丰度发生统计学显着变化(p值≤0.05)。蛋白质的功能注释在各个时间点之间表现出明显的表达变化,从而鉴定了与不同细胞过程有关的蛋白质簇,这些细胞过程包括干扰素和白介素信号传导,内吞作用,ER-吞噬途径和抗原呈递。在SWATH-MS中,主要的组织相容性复合体(MHC)I类蛋白在24 ath高度上调,而在此期间MHC II类蛋白表现出相对较少的变化。这项研究为抗原处理和呈递过程中moDC中发生的全球蛋白质组学变化提供了新的详细见解,并进一步证明了SWATH-MS在定量研究细胞过程中涉及的蛋白质方面的潜力。

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