The adaptor protein TRADD is essential for TNF-like ligand 1A/death receptor 3 signaling.

TitleThe adaptor protein TRADD is essential for TNF-like ligand 1A/death receptor 3 signaling.
Publication TypeJournal Article
Year of Publication2011
AuthorsPobezinskaya YL, Choksi S, Morgan MJ, Cao X, Liu Z-G
JournalJ Immunol
Volume186
Issue9
Pagination5212-6
Date Published2011 May 1
ISSN1550-6606
KeywordsAnimals, Blotting, Western, Cell Separation, Electrophoretic Mobility Shift Assay, Flow Cytometry, Immunoprecipitation, Lymphocyte Activation, Mice, Mice, Knockout, Receptors, Tumor Necrosis Factor, Member 25, Signal Transduction, T-Lymphocytes, TNF Receptor-Associated Death Domain Protein, Tumor Necrosis Factor Ligand Superfamily Member 15
Abstract

TNFR-associated death domain protein (TRADD) is a key effector protein of TNFR1 signaling. However, the role of TRADD in other death receptor (DR) signaling pathways, including DR3, has not been completely characterized. Previous studies using overexpression systems suggested that TRADD is recruited to the DR3 complex in response to the DR3 ligand, TNF-like ligand 1A (TL1A), indicating a possible role in DR3 signaling. Using T cells from TRADD knockout mice, we demonstrate in this study that the response of both CD4(+) and CD8(+) T cells to TL1A is dependent upon the presence of TRADD. TRADD knockout T cells therefore lack the appropriate proliferative response to TL1A. Moreover, in the absence of TRADD, both the stimulation of MAPK signaling and activation of NF-κB in response to TL1A are dramatically reduced. Unsurprisingly, TRADD is required for recruitment of receptor interacting protein 1 and TNFR-associated factor 2 to the DR3 signaling complex and for the ubiquitination of receptor interacting protein 1. Thus, our findings definitively establish an essential role of TRADD in DR3 signaling.

DOI10.4049/jimmunol.1002374
Alternate JournalJ. Immunol.
PubMed ID21421854