Division of Cell Biology and Centre for Biomedical Genetics, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.
Cell. 2011 Apr 15;145(2):268-83. doi: 10.1016/j.cell.2011.03.023. Epub 2011 Mar 31.
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.
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。