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幽门螺杆菌cagA阴性同基因突变体诱导胃上皮细胞分泌白细胞介素-8

Induction of interleukin-8 secretion from gastric epithelial cells by a cagA negative isogenic mutant of Helicobacter pylori.

作者信息

Crabtree J E, Xiang Z, Lindley I J, Tompkins D S, Rappuoli R, Covacci A

机构信息

Division of Medicine, St James's University Hospital, Leeds.

出版信息

J Clin Pathol. 1995 Oct;48(10):967-9. doi: 10.1136/jcp.48.10.967.

Abstract

The ability of Helicobacter pylori strains to induce interleukin-8 (IL-8) gene expression and protein secretion from gastric epithelial cell lines in vitro is variable. This cellular response is associated with bacterial expression of the CagA protein present in type I H pylori strains. To determine the role of CagA in this host cell response, an isogenic cagA negative mutant, N6.XA3, was constructed. The cagA negative isogenic mutant and the wild-type parental cagA positive strain, N6, were cocultured with AGS, ST-42 and KATO-3 gastric epithelial cell lines and secreted interleukin-8 assayed by enzyme linked immunosorbent assay. In all three cell lines there was no significant difference in the IL-8 secretion induced by the cagA negative isogenic mutant, N6.XA3, and the wild-type parent strain, N6. These studies show that CagA is not the inducer of IL-8 secretion from gastric epithelial cells. As all wild-type CagA positive strains studied to date induce IL-8, the bacterial factor(s) inducing this inflammatory response is closely associated with the expression of CagA.

摘要

幽门螺杆菌菌株在体外诱导胃上皮细胞系白细胞介素-8(IL-8)基因表达和蛋白质分泌的能力存在差异。这种细胞反应与I型幽门螺杆菌菌株中存在的CagA蛋白的细菌表达有关。为了确定CagA在这种宿主细胞反应中的作用,构建了一个同基因的cagA阴性突变体N6.XA3。将cagA阴性同基因突变体和野生型亲代cagA阳性菌株N6与AGS、ST-42和KATO-3胃上皮细胞系共培养,并通过酶联免疫吸附测定法检测分泌的白细胞介素-8。在所有三种细胞系中,cagA阴性同基因突变体N6.XA3和野生型亲代菌株N6诱导的IL-8分泌没有显著差异。这些研究表明,CagA不是胃上皮细胞IL-分泌的诱导剂。由于迄今为止研究的所有野生型CagA阳性菌株都能诱导IL-8,诱导这种炎症反应的细菌因子与CagA的表达密切相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fb7/502959/325a8b9b687c/jclinpath00235-0086-a.jpg

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