| Literature DB >> 18256385 |
Andreas Till1, Philip Rosenstiel, Karen Bräutigam, Christian Sina, Gunnar Jacobs, Hans-Heinrich Oberg, Dirk Seegert, Trinad Chakraborty, Stefan Schreiber.
Abstract
NOD2 is an intracellular receptor for the bacterial cell wall component muramyl dipeptide. Mutations in the leucine-rich repeat region of NOD2, which lead to an impaired recognition of muramyl dipeptide, have been associated with chronic inflammatory diseases of barrier organs such as Crohn disease, asthma and atopic eczema. In this study we identify CD147 (also known as BSG and EMMPRIN), a membrane-bound regulator of cellular migration, differentiation and inflammatory processes, as a protein interaction partner of NOD2. We demonstrate a complex influence of the CD147-NOD2 interaction on NOD2-dependent signaling responses. We show that CD147 itself acts as an enhancer of the invasion of Listeria monocytogenes, an intracellular bacterial pathogen. We propose that the CD147-NOD2 interaction serves as a molecular guide to regulate NOD2 function at sites of pathogen invasion.Entities:
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Year: 2008 PMID: 18256385 DOI: 10.1242/jcs.016980
Source DB: PubMed Journal: J Cell Sci ISSN: 0021-9533 Impact factor: 5.285