Brosbøl-Ravnborg A, Hvas C L, Agnholt J, Dahlerup J F, Vind I, Till A, Rosenstiel P, Höllsberg P
Institute of Medical Microbiology and Immunology, University of Aarhus, Aarhus, Denmark.
Clin Exp Immunol. 2009 Mar;155(3):487-95. doi: 10.1111/j.1365-2249.2008.03850.x. Epub 2008 Dec 15.
Pattern recognition receptors (PRRs) are an integral part of the innate immune system and govern the early control of foreign microorganisms. Single nucleotide polymorphisms (SNPs) in the intracellular pattern recognition receptor nucleotide-binding oligomerization domain-containing protein (NOD2, nucleotide oligomerization domain 2) are associated with Crohn's disease (CD). We investigated the impact of NOD2 polymorphisms on cytokine secretion and proliferation of peripheral blood mononuclear cells (PBMCs) in response to Toll-like receptor (TLR) and NOD2 ligands. Based on NOD2 SNP analyses, 41 CD patients and 12 healthy controls were studied. PBMCs were stimulated with NOD2 and TLR ligands. After 18 h culture supernatants were measured using multiplex assays for the presence of human cytokines granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin (IL)-1 beta and tumour necrosis factor (TNF)-alpha. In CD patients, TLR-induced GM-CSF secretion was impaired by both NOD2-dependent and -independent mechanisms. Moreover, TNF-alpha production was induced by a TLR-2 ligand, but a down-regulatory function by the NOD2 ligand, muramyl dipeptide, was impaired significantly in CD patients. Intracellular TLR ligands had minimal effect on GM-CSF, TNF-alpha and IL-1beta secretion. CD patients with NOD2 mutations were able to secrete TNF-alpha, but not GM-CSF, upon stimulation with NOD2 and TLR-7 ligands. CD patients have impaired GM-CSF secretion via NOD2-dependent and -independent pathways and display an impaired NOD2-dependent down-regulation of TNF-alpha secretion. The defect in GM-CSF secretion suggests a hitherto unknown role of NOD2 in the pathogenesis of CD and is consistent with the hypothesis that impaired GM-CSF secretion in part constitutes a NOD2-dependent disease risk factor.
模式识别受体(PRRs)是固有免疫系统的一个组成部分,负责对外来微生物的早期控制。细胞内模式识别受体含核苷酸结合寡聚化结构域蛋白(NOD2,核苷酸寡聚化结构域2)中的单核苷酸多态性(SNPs)与克罗恩病(CD)相关。我们研究了NOD2多态性对 Toll 样受体(TLR)和 NOD2 配体刺激下外周血单核细胞(PBMCs)细胞因子分泌和增殖的影响。基于 NOD2 SNP 分析,对 41 例 CD 患者和 12 例健康对照进行了研究。用 NOD2 和 TLR 配体刺激 PBMCs。培养 18 小时后,使用多重检测法检测培养上清液中人类细胞因子粒细胞-巨噬细胞集落刺激因子(GM-CSF)、白细胞介素(IL)-1β和肿瘤坏死因子(TNF)-α的存在情况。在 CD 患者中,TLR 诱导的 GM-CSF 分泌通过 NOD2 依赖和非依赖机制受损。此外,TLR-2 配体可诱导 TNF-α产生,但在 CD 患者中,NOD2 配体胞壁酰二肽的下调功能明显受损。细胞内 TLR 配体对 GM-CSF、TNF-α和 IL-1β分泌的影响最小。NOD2 突变的 CD 患者在受到 NOD2 和 TLR-7 配体刺激后能够分泌 TNF-α,但不能分泌 GM-CSF。CD 患者通过 NOD2 依赖和非依赖途径的 GM-CSF 分泌受损,并且 NOD2 依赖的 TNF-α分泌下调功能受损。GM-CSF 分泌缺陷提示 NOD2 在 CD 发病机制中具有迄今未知的作用,这与以下假设一致,即 GM-CSF 分泌受损部分构成了 NOD2 依赖的疾病风险因素。