COP9 signalosome controls the Carma1–Bcl10–Malt1 complex upon T‐cell stimulation |
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Authors: | Verena Welteke Andrea Eitelhuber Michael Düwel Katrin Schweitzer Michael Naumann Daniel Krappmann |
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Affiliation: | 1.Department Cellular Signal Integration, Helmholtz Zentrum München—German Research Center for Environmental Health, Institute of Toxicology, Ingolstädter Landstrasse 1, 85764 Neuherberg, Germany;2.Medical Faculty, Institute of Experimental Internal Medicine, Otto von Guericke University, Leipziger Strasse 44, 39120 Magdeburg, Germany |
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Abstract: | The Carma1–Bcl10–Malt1 (CBM) complex connects T‐cell receptor (TCR) signalling to the canonical IκB kinase (IKK)/NF (nuclear factor)‐κB pathway. Earlier studies have indicated that the COP9 signalosome (CSN), a pleiotropic regulator of the ubiquitin/26S proteasome system, controls antigen responses in T cells. The CSN is required for the degradation of the NF‐κB inhibitor IκBα, but other molecular targets involved in T‐cell signalling remained elusive. Here, we identify the CSN subunit 5 (CSN5) as a new interactor of Malt1 and Carma1. T‐cell activation triggers the recruitment of the CSN to the CBM complex, and CSN downregulation impairs TCR‐induced IKK activation. Furthermore, the CSN is required for maintaining the stability of Bcl10 in response to T‐cell activation. Taken together, our data provide evidence for a functional link between the evolutionarily conserved CSN and the adaptive immunoregulatory CBM complex in T cells. |
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Keywords: | COP9 signalosome signalling T‐cell activation |
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