Title
Integrating signals from the T-cell receptor and the interleukin-2 receptor.
Abstract
T cells orchestrate the adaptive immune response, making them targets for immunotherapy. Although immunosuppressive therapies prevent disease progression, they also leave patients susceptible to opportunistic infections. To identify novel drug targets, we established a logical model describing T-cell receptor (TCR) signaling. However, to have a model that is able to predict new therapeutic approaches, the current drug targets must be included. Therefore, as a next step we generated the interleukin-2 receptor (IL-2R) signaling network and developed a tool to merge logical models. For IL-2R signaling, we show that STAT activation is independent of both Src-and PI3-kinases, while ERK activation depends upon both kinases and additionally requires novel PKCs. In addition, our merged model correctly predicted TCR-induced STAT activation. The combined network also allows information transfer from one receptor to add detail to another, thereby predicting that LAT mediates JNK activation in IL-2R signaling. In summary, the merged model not only enables us to unravel potential cross-talk, but it also suggests new experimental designs and provides a critical step towards designing strategies to reprogram T cells.
Year
DOI
Venue
2011
10.1371/journal.pcbi.1002121
PLOS COMPUTATIONAL BIOLOGY
Keywords
Field
DocType
signal transduction,information transfer,experimental design,adaptive immunity,protein kinase c,drug targeting,t cell receptor
T-cell receptor,Receptor Cross-Talk,Interleukin 2,Biology,Acquired immune system,MAPK/ERK pathway,Signal transduction,Bioinformatics,PKCS,stat
Journal
Volume
Issue
ISSN
7
8
1553-7358
Citations 
PageRank 
References 
2
0.60
5
Authors
11