Till Andreas, Rosenstiel Philip, Bräutigam Karen, Sina Christian, Jacobs Gunnar, Oberg Hans-Heinrich, Seegert Dirk, Chakraborty Trinad, Schreiber Stefan
Institute for Clinical Molecular Biology, University Hospital Schleswig-Holstein, Campus Kiel, Schittenhelmstr 12, Kiel, Germany.
J Cell Sci. 2008 Feb 15;121(Pt 4):487-95. doi: 10.1242/jcs.016980.
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.
NOD2是细菌细胞壁成分胞壁酰二肽的细胞内受体。NOD2富含亮氨酸重复序列区域的突变会导致对胞壁酰二肽的识别受损,这与屏障器官的慢性炎症性疾病有关,如克罗恩病、哮喘和特应性皮炎。在本研究中,我们鉴定出CD147(也称为BSG和EMMPRIN),一种细胞迁移、分化和炎症过程的膜结合调节因子,作为NOD2的蛋白质相互作用伙伴。我们证明了CD147-NOD2相互作用对NOD2依赖性信号反应具有复杂的影响。我们表明,CD147本身作为细胞内细菌病原体单核细胞增生李斯特菌入侵的增强子。我们提出,CD147-NOD2相互作用作为一种分子导向,在病原体入侵部位调节NOD2功能。