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全基因组多维 RNAi 筛选揭示了控制 MHC II 类抗原呈递的途径。

A Genome-wide multidimensional RNAi screen reveals pathways controlling MHC class II antigen presentation.

机构信息

Division of Cell Biology and Centre for Biomedical Genetics, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.

出版信息

Cell. 2011 Apr 15;145(2):268-83. doi: 10.1016/j.cell.2011.03.023. Epub 2011 Mar 31.

Abstract

MHC class II molecules (MHC-II) present peptides to T helper cells to facilitate immune responses and are strongly linked to autoimmune diseases. To unravel processes controlling MHC-II antigen presentation, we performed a genome-wide flow cytometry-based RNAi screen detecting MHC-II expression and peptide loading followed by additional high-throughput assays. All data sets were integrated to answer two fundamental questions: what regulates tissue-specific MHC-II transcription, and what controls MHC-II transport in dendritic cells? MHC-II transcription was controlled by nine regulators acting in feedback networks with higher-order control by signaling pathways, including TGFβ. MHC-II transport was controlled by the GTPase ARL14/ARF7, which recruits the motor myosin 1E via an effector protein ARF7EP. This complex controls movement of MHC-II vesicles along the actin cytoskeleton in human dendritic cells (DCs). These genome-wide systems analyses have thus identified factors and pathways controlling MHC-II transcription and transport, defining targets for manipulation of MHC-II antigen presentation in infection and autoimmunity.

摘要

MHC II 类分子 (MHC-II) 将肽呈递给辅助性 T 细胞以促进免疫反应,并且与自身免疫性疾病密切相关。为了揭示控制 MHC-II 抗原呈递的过程,我们进行了基于全基因组流式细胞术的 RNAi 筛选,以检测 MHC-II 的表达和肽负载,然后进行额外的高通量检测。所有数据集都进行了整合,以回答两个基本问题:是什么调节组织特异性 MHC-II 转录,以及是什么控制树突状细胞中的 MHC-II 转运?MHC-II 转录由九个调节剂控制,这些调节剂在信号通路的高阶控制下形成反馈网络,包括 TGFβ。MHC-II 转运由 GTPase ARL14/ARF7 控制,该蛋白通过效应蛋白 ARF7EP 招募马达肌球蛋白 1E。该复合物控制着人类树突状细胞 (DC) 中 MHC-II 囊泡沿着肌动蛋白细胞骨架的运动。这些全基因组系统分析已经确定了控制 MHC-II 转录和转运的因素和途径,为感染和自身免疫中 MHC-II 抗原呈递的操纵定义了目标。

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