Integrative biology of T cell activation

被引:84
作者
Malissen, Bernard [1 ,2 ,3 ,4 ,5 ,6 ]
Gregoire, Claude [1 ,2 ,3 ]
Malissen, Marie [1 ,2 ,3 ,4 ,5 ,6 ]
Roncagalli, Romain [1 ,2 ,3 ]
机构
[1] Aix Marseille Univ, UM2, Ctr Immunol Marseille Luminy, Marseille, France
[2] INSERM, U1104, F-13258 Marseille, France
[3] CNRS, UMR7280, Marseille, France
[4] Aix Marseille Univ, UM2, Ctr Immunophen, Marseille, France
[5] INSERM, US012, F-13258 Marseille, France
[6] CNRS, UMS3367, Marseille, France
基金
欧洲研究理事会;
关键词
ADAPTER PROTEIN LAT; KINASE PKC-THETA; LYMPHOPROLIFERATIVE DISORDER; PHOSPHOPROTEOMIC ANALYSIS; SIGNALING MOLECULES; MULTIPOINT BINDING; CD8(+) T; RECEPTOR; TCR; ANTIGEN;
D O I
10.1038/ni.2959
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The activation of T cells mediated by the T cell antigen receptor (TCR) requires the interaction of dozens of proteins, and its malfunction has pathological consequences. Our major focus is on new developments in the systems-level understanding of the TCR signal-transduction network. To make sense of the formidable complexity of this network, we argue that 'fine-grained' methods are needed to assess the relationships among a few components that interact on a nanometric scale, and those should be integrated with high-throughput '-omic' approaches that simultaneously capture large numbers of parameters. We illustrate the utility of this integrative approach with the transmembrane signaling protein Lat, which is a key signaling hub of the TCR signal-transduction network, as a connecting thread.
引用
收藏
页码:790 / 797
页数:8
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