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Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-57688

Gerlach, B; Cordier, S M; Schmukle, A C; Emmerich, C H; Rieser, E; Haas, T L; Webb, A I; Rickard, J A; Anderton, H; Wong, W W L; Nachbur, U; Gangoda, L; Warnken, U; Purcell, A W; Silke, J; Walczak, H (2011). Linear ubiquitination prevents inflammation and regulates immune signalling. Nature, 471(7340):591-598.

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Abstract

Members of the tumour necrosis factor (TNF) receptor superfamily have important functions in immunity and inflammation. Recently linear ubiquitin chains assembled by a complex containing HOIL-1 and HOIP (also known as RBCK1 and RNF31, respectively) were implicated in TNF signalling, yet their relevance in vivo remained uncertain. Here we identify SHARPIN as a third component of the linear ubiquitin chain assembly complex, recruited to the CD40 and TNF receptor signalling complexes together with its other constituents, HOIL-1 and HOIP. Mass spectrometry of TNF signalling complexes revealed RIP1 (also known as RIPK1) and NEMO (also known as IKKγ or IKBKG) to be linearly ubiquitinated. Mutation of the Sharpin gene (Sharpin(cpdm/cpdm)) causes chronic proliferative dermatitis (cpdm) characterized by inflammatory skin lesions and defective lymphoid organogenesis. Gene induction by TNF, CD40 ligand and interleukin-1β was attenuated in cpdm-derived cells which were rendered sensitive to TNF-induced death. Importantly, Tnf gene deficiency prevented skin lesions in cpdm mice. We conclude that by enabling linear ubiquitination in the TNF receptor signalling complex, SHARPIN interferes with TNF-induced cell death and, thereby, prevents inflammation. Our results provide evidence for the relevance of linear ubiquitination in vivo in preventing inflammation and regulating immune signalling.

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Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > University Hospital Zurich > Institute of Experimental Immunology
DDC:570 Life sciences; biology
610 Medicine & health
Language:English
Date:2011
Deposited On:01 Feb 2012 20:33
Last Modified:08 Dec 2013 12:37
Publisher:Nature Publishing Group
ISSN:0028-0836
Publisher DOI:10.1038/nature09816
PubMed ID:21455173

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