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首页> 外文期刊>Infection and immunity >Enteropathogenic Escherichia coli Infection Induces Expression of the Early Growth Response Factor by Activating Mitogen-Activated Protein Kinase Cascades in Epithelial Cells
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Enteropathogenic Escherichia coli Infection Induces Expression of the Early Growth Response Factor by Activating Mitogen-Activated Protein Kinase Cascades in Epithelial Cells

机译:肠致病性大肠杆菌感染通过激活上皮细胞中的丝裂原活化蛋白激酶级联反应诱导早期生长反应因子的表达。

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摘要

Enteropathogenic Escherichia coli (EPEC) is an extracellular bacterial pathogen that infects the human intestinal epithelium and is a major cause of infantile diarrhea in developing countries. EPEC belongs to the group of attaching and effacing (A/E) pathogens. It uses a type III secretion system to deliver proteins into the host cell that mediate signal transduction events in host cells. We used gene array technology to study epithelial cell responses to EPEC infection at the level of gene expression. We found that EPEC induces the expression of several genes in infected HeLa cells by a lipopolysaccharide (LPS)-independent mechanism, including cytokines and early growth response factor 1 (Egr-1). The transcription factor Egr-1 is an immediate-early-induced gene that is activated in most cell types in response to stress. EPEC-induced upregulation ofegr-1 is mediated by the activation of the MEK/extracellular signal-regulated kinase signal transduction pathway and is dependent on the type III secretion system. egr-1 is also induced during infection of mice by the A/E pathogenCitrobacter rodentium, suggesting that both Egr-1 and the activation of this mitogen-activated protein kinase signal transduction pathway may play a role in disease.
机译:肠致病性大肠埃希菌(EPEC)是一种细胞外细菌病原体,可感染人的肠上皮,并且是发展中国家婴儿腹泻的主要原因。 EPEC属于附着和消失(A / E)病原体组。它使用III型分泌系统将蛋白质传递到宿主细胞中,从而介导宿主细胞中的信号转导事件。我们使用基因阵列技术在基因表达水平上研究上皮细胞对EPEC感染的反应。我们发现EPEC通过不依赖脂多糖(LPS)的机制诱导感染的HeLa细胞中几个基因的表达,包括细胞因子和早期生长反应因子1(Egr-1)。转录因子Egr-1是一种立即早期诱导的基因,可在大多数细胞类型中响应压力而被激活。 EPEC诱导的 egr-1 的上调是由MEK /细胞外信号调节激酶信号转导途径的激活介导的,并且依赖于III型分泌系统。 A / E病原菌 Citrobacter rodentium 在小鼠感染过程中也诱导了 egr-1 ,这表明Egr-1和此丝裂原激活的蛋白激酶信号均被激活转导途径可能在疾病中起作用。

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