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Regulation of IL-8 and IL-1β expression in Crohn's disease associated NOD2/CARD15 mutations

Regulation of IL-8 and IL-1β expression in Crohn's disease associated NOD2/CARD15 mutations Crohn's disease (CD) is a chronic inflammation affecting the gastrointestinal tract. Three mutations (Arg702Trp, Gly908Arg and Leu1007fsinsC) within the NOD2/CARD15 gene increase CD susceptibility. Here, we define cytokine regulation in primary human mononuclear cells, with muramyl dipeptide (MDP), the minimal NOD2/CARD15 activating component of peptidoglycan. By microarray, MDP induces a broad array of transcripts, including interleukin 1β (IL-1β) and interleukin 8 (IL-8). Leu1007fsinsC homozygotes demonstrated decreased transcriptional response to MDP. Electromobility shift assay demonstrated that MDP-induced NF-κB activation is mediated via p50 and p65 subunits, but not RelB or c-Rel. In wild-type individuals, MDP-induced IL-8 protein expression with a greater response to high dose (1 µg/ml) compared with low-dose (10 ng/ml) MDP. At low MDP doses, in all homozygotes, we observed no induction of IL-8 protein. With high doses of MDP, Leu1007fsinsC homozygotes showed no induction. Modest induction of IL-8 protein was observed in Gly908Arg and Arg702Trp homozygotes, indicating varying MDP sensitivity of the CD-associated mutations. In wild-type healthy control, CD and ulcerative colitis individuals, low-dose MDP and TNFα alone results in only modest IL-1β protein induction. With MDP plus TNFα, there is a synergistic induction of IL-1β secretion. In Leu1007fsinsC homozygotes, there is a profound defect in IL-1β secretion, despite marked induction of IL-1β mRNA. These findings demonstrate post-transcriptional dependency on the NOD2/CARD15 pathway for IL-1β secretion with MDP and TNFα treatment. Taken together, these studies suggest that a signaling defect of innate immunity to MDP may be an essential underlying defect in the pathogenesis of some CD patients. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Human Molecular Genetics Oxford University Press

Regulation of IL-8 and IL-1β expression in Crohn's disease associated NOD2/CARD15 mutations

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References (50)

Publisher
Oxford University Press
Copyright
Human Molecular Genetics, Vol. 13, No. 16 © Oxford University Press 2004; all rights reserved
ISSN
0964-6906
eISSN
1460-2083
DOI
10.1093/hmg/ddh182
pmid
15198989
Publisher site
See Article on Publisher Site

Abstract

Crohn's disease (CD) is a chronic inflammation affecting the gastrointestinal tract. Three mutations (Arg702Trp, Gly908Arg and Leu1007fsinsC) within the NOD2/CARD15 gene increase CD susceptibility. Here, we define cytokine regulation in primary human mononuclear cells, with muramyl dipeptide (MDP), the minimal NOD2/CARD15 activating component of peptidoglycan. By microarray, MDP induces a broad array of transcripts, including interleukin 1β (IL-1β) and interleukin 8 (IL-8). Leu1007fsinsC homozygotes demonstrated decreased transcriptional response to MDP. Electromobility shift assay demonstrated that MDP-induced NF-κB activation is mediated via p50 and p65 subunits, but not RelB or c-Rel. In wild-type individuals, MDP-induced IL-8 protein expression with a greater response to high dose (1 µg/ml) compared with low-dose (10 ng/ml) MDP. At low MDP doses, in all homozygotes, we observed no induction of IL-8 protein. With high doses of MDP, Leu1007fsinsC homozygotes showed no induction. Modest induction of IL-8 protein was observed in Gly908Arg and Arg702Trp homozygotes, indicating varying MDP sensitivity of the CD-associated mutations. In wild-type healthy control, CD and ulcerative colitis individuals, low-dose MDP and TNFα alone results in only modest IL-1β protein induction. With MDP plus TNFα, there is a synergistic induction of IL-1β secretion. In Leu1007fsinsC homozygotes, there is a profound defect in IL-1β secretion, despite marked induction of IL-1β mRNA. These findings demonstrate post-transcriptional dependency on the NOD2/CARD15 pathway for IL-1β secretion with MDP and TNFα treatment. Taken together, these studies suggest that a signaling defect of innate immunity to MDP may be an essential underlying defect in the pathogenesis of some CD patients.

Journal

Human Molecular Genetics – Oxford University Press

Published: Aug 15, 2004

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