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

• Published in: Human molecular genetics Vol. 13; no. 16; pp. 1715 - 1725
• Main Author: Li, J.
• Format: Journal Article
• Language: English
• Published: Oxford Oxford Publishing Limited (England) 15.06.2004
• ISSN: 1460-2083; 0964-6906; 1460-2083
• DOI: 10.1093/hmg/ddh182

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 1[beta] (IL-1[beta]) and interleukin 8 (IL-8). Leu1007fsinsC homozygotes demonstrated decreased transcriptional response to MDP. Electromobility shift assay demonstrated that MDP-induced NF-[kappa]B 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 TNF[alpha] alone results in only modest IL-1[beta] protein induction. With MDP plus TNF[alpha], there is a synergistic induction of IL-1[beta] secretion. In Leu1007fsinsC homozygotes, there is a profound defect in IL-1[beta] secretion, despite marked induction of IL-1[beta] mRNA. These findings demonstrate post-transcriptional dependency on the NOD2/CARD15 pathway for IL-1[beta] secretion with MDP and TNF[alpha] 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.