Watson James L, McKay Derek M
Intestinal Disease Research Programme, Department of Pathology and Molecular Medicine, McMaster University, HSC-3N5C, 1200 Main Street West, Hamilton, Ontario, Canada L8N 3Z5.
Clin Chim Acta. 2006 Feb;364(1-2):1-11. doi: 10.1016/j.cca.2005.05.017. Epub 2005 Sep 8.
Both the endogenous commensal flora and a dysregulated mucosal immune response have been implicated as contributing to the pathogenesis of human intestinal disease. Unmethylated cytosine-guanine (CpG)-containing DNA, the ligand for Toll-like receptor 9 (TLR9), is a recently recognized microbial product with immunostimulatory and immunoregulatory effects. TLR9 is expressed by many cell types located in the intestine, including epithelial cells and classical immune cells. The physiological impact of the juxtaposition of these factors (bacterial DNA and responsive cells) in the gut therefore bears consideration. Here we discuss studies that examine the interaction between CpG DNA and the intestine, focusing on activation of epithelial cells, administration of CpG-containing oligonucleotides as therapy for experimental inflammatory enteropathies, and the role of CpG DNA in mediating the beneficial effects of bacterial probiotics.
内源性共生菌群和失调的黏膜免疫反应均被认为与人类肠道疾病的发病机制有关。含未甲基化胞嘧啶-鸟嘌呤(CpG)的DNA是Toll样受体9(TLR9)的配体,是一种最近被认识的具有免疫刺激和免疫调节作用的微生物产物。TLR9由位于肠道的多种细胞类型表达,包括上皮细胞和经典免疫细胞。因此,肠道中这些因素(细菌DNA和反应性细胞)并列所产生的生理影响值得考虑。在此,我们讨论研究CpG DNA与肠道之间相互作用的研究,重点关注上皮细胞的激活、含CpG的寡核苷酸作为实验性炎症性肠病治疗方法的应用,以及CpG DNA在介导细菌益生菌有益作用中的作用。