A Genome-wide Multidimensional RNAi Screen Reveals Pathways Controlling MHC Class II Antigen Presentation

被引:118
作者
Paul, Petra [1 ,2 ]
van den Hoorn, Tineke [1 ,2 ]
Jongsma, Marlieke L. M. [1 ,2 ]
Bakker, Mark J. [1 ,2 ]
Hengeveld, Rutger [1 ,2 ]
Janssen, Lennert [1 ,2 ]
Cresswell, Peter [4 ]
Egan, David A. [3 ]
van Ham, Marieke [5 ]
ten Brinke, Anja [5 ]
Ovaa, Huib [1 ,2 ]
Beijersbergen, Roderick L. [3 ]
Kuijl, Coenraad [1 ,2 ]
Neefjes, Jacques [1 ,2 ]
机构
[1] Netherlands Canc Inst, Div Cell Biol, NL-1066 CX Amsterdam, Netherlands
[2] Netherlands Canc Inst, Ctr Biomed Genet, NL-1066 CX Amsterdam, Netherlands
[3] Netherlands Canc Inst, Robot & Screening Ctr, NL-1066 CX Amsterdam, Netherlands
[4] Yale Univ, Howard Hughes Med Inst, Dept Immunobiol, Sch Med, New Haven, CT 06520 USA
[5] Univ Amsterdam, Acad Med Ctr, Dept Immunopathol, Sanquin Res & Landsteiner Lab, NL-1066 CX Amsterdam, Netherlands
关键词
HLA-DR MOLECULES; DENDRITIC CELLS; MYOSIN; 1E; TRANSPORT; PROTEIN; EXPRESSION; MEMBRANE; INHIBITION; MATURATION; COMPLEXES;
D O I
10.1016/j.cell.2011.03.023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 TGF beta. 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.
引用
收藏
页码:268 / 283
页数:16
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