Nod2 Mutation in Crohn's Disease Potentiates NF-κB Activity and IL-1ß Processing
Sanford Burnham Prebys Medical Discovery Institute · University of California San Diego
Abstract
Variants of NOD2, an intracellular sensor of bacteria-derived muramyl dipeptide (MDP), increase susceptibility to Crohn's disease (CD). These variants are thought to be defective in activation of nuclear factor kappaB (NF-kappaB) and antibacterial defenses, but CD clinical specimens display elevated NF-kappaB activity. To illuminate the pathophysiological function of NOD2, we introduced such a variant to the mouse Nod2 locus. Mutant mice exhibited elevated NF-kappaB activation in response to MDP and more efficient processing and secretion of the cytokine interleukin-1beta (IL-1beta). These effects are linked to increased susceptibility to bacterial-induced intestinal inflammation and identify NOD2 as a…
Citation impact
- FWCI
- 60.33
- Percentile
- 100%
- References
- 23
Authors
8- SMShin Maeda
Sanford Burnham Prebys Medical Discovery Institute, University of California San Diego
- LHLi-Chung HsuCorresponding
Sanford Burnham Prebys Medical Discovery Institute, University of California San Diego
- HLHongjun LiuCorresponding
Sanford Burnham Prebys Medical Discovery Institute, University of California San Diego
- LALaurie A. Bankston
Sanford Burnham Prebys Medical Discovery Institute, University of California San Diego
- MIMitsutoshi Iimura
Sanford Burnham Prebys Medical Discovery Institute, University of California San Diego
Topics & keywords
- NOD2
- Muramyl dipeptide
- Crohn's disease
- Secretion
- Mutant
- Regulator
- Inflammation
- Cytokine
- Good health and well-being