Author:
Ghalandary Maryam,Li Yue,Fröhlich Thomas,Magg Thomas,Liu Yanshan,Rohlfs Meino,Hollizeck Sebastian,Conca Raffaele,Schwerd Tobias,Uhlig Holm H.,Bufler Philip,Koletzko Sibylle,Muise Aleixo M.,Snapper Scott B.,Hauck Fabian,Klein Christoph,Kotlarz Daniel
Abstract
AbstractNOD2 polymorphisms may affect sensing of the bacterial muramyl dipeptide (MDP) and trigger perturbed inflammatory responses. Genetic screening of a patient with immunodeficiency and enteropathy revealed a rare homozygous missense mutation in the first CARD domain of NOD2 (ENST00000300589; c.160G > A, p.E54K). Biochemical assays confirmed impaired NOD2-dependent signaling and proinflammatory cytokine production in patient’s cells and heterologous cellular models with overexpression of the NOD2 mutant. Immunoprecipitation-coupled mass spectrometry unveiled the ATPase valosin-containing protein (VCP) as novel interaction partner of wildtype NOD2, while the binding to the NOD2 variant p.E54K was abrogated. Knockdown of VCP in coloncarcinoma cells led to impaired NF-κB activity and IL8 expression upon MDP stimulation. In contrast, tunicamycin-induced ER stress resulted in increased IL8, CXCL1, and CXCL2 production in cells with knockdown of VCP, while enhanced expression of these proinflammatory molecules was abolished upon knockout of NOD2. Taken together, these data suggest that VCP-mediated inflammatory responses upon ER stress are NOD2-dependent.
Publisher
Springer Science and Business Media LLC
Cited by
2 articles.
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