Journal article
TRAF3, ubiquitination, and B-lymphocyte regulation
Immunological reviews, Vol.266(1), pp.46-55
07/2015
DOI: 10.1111/imr.12299
PMCID: PMC4473794
PMID: 26085206
Abstract
The signaling adapter protein tumor necrosis factor receptor (TNFR)-associated factor 3 (TRAF3) is both modified by and contributes to several types of ubiquitination events. TRAF3 plays a variety of context-dependent regulatory roles in all types of immune cells. In B lymphocytes, TRAF3 contributes to regulation of signaling by members of both the TNFR superfamily and innate immune receptors. TRAF3 also plays a unique cell type-specific and critical role in the restraint of B-cell homeostatic survival, a role with important implications for both B-cell differentiation and the pathogenesis of B-cell malignancies. This review focuses upon the relationship between ubiquitin and TRAF3, and how this contributes to multiple functions of TRAF3 in the regulation of signal transduction, transcriptional activation, and effector functions of B lymphocytes.
Details
- Title: Subtitle
- TRAF3, ubiquitination, and B-lymphocyte regulation
- Creators
- Wai W Lin - The Graduate Program in Immunology, University of Iowa, Iowa City, IA, USABruce S Hostager - Department of Pediatrics, University of Iowa, Iowa City, IA, USAGail A Bishop - VA Medical Center, University of Iowa, Iowa City, IA, USA
- Resource Type
- Journal article
- Publication Details
- Immunological reviews, Vol.266(1), pp.46-55
- DOI
- 10.1111/imr.12299
- PMID
- 26085206
- PMCID
- PMC4473794
- NLM abbreviation
- Immunol Rev
- ISSN
- 0105-2896
- eISSN
- 1600-065X
- Publisher
- England
- Grant note
- R01 AI28847 / NIAID NIH HHS P30 ES005605 / NIEHS NIH HHS R01 AI028847 / NIAID NIH HHS CA97274 / NCI NIH HHS CA099997 / NCI NIH HHS I01 BX001702 / BLRD VA R01 CA099997 / NCI NIH HHS P30 CA086862 / NCI NIH HHS P50 CA097274 / NCI NIH HHS
- Language
- English
- Date published
- 07/2015
- Academic Unit
- Microbiology and Immunology; President
- Record Identifier
- 9984002397502771
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