首页> 外文期刊>Comparative and functional genomics >Preliminary Characterization of the Transcriptional Response of the Porcine Intestinal Cell Line IPEC-J2 to EnterotoxigenicEscherichia coli,Escherichia coli, andE. coliLipopolysaccharide
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Preliminary Characterization of the Transcriptional Response of the Porcine Intestinal Cell Line IPEC-J2 to EnterotoxigenicEscherichia coli,Escherichia coli, andE. coliLipopolysaccharide

机译:猪肠道细胞系IPEC-J2对产肠毒素的大肠埃希氏菌,大肠埃希氏菌和大肠杆菌的转录反应的初步表征。大肠脂多糖

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IPEC-J2, a promisingin vitromodel system, is not well characterized especially on the transcriptional level, in contrast to human counterparts. The aim of this study was to characterize the gene expression in IPEC-J2 cells when coincubated with enterotoxigenicEscherichia coli(ETEC), nonpathogenicE. coli, andE. coliendotoxin. Apical infection of polarized IPEC-J2 monolayers caused a time-dependent decrease in transepithelial electrical resistance (TEER). Microarray analysis showed up-regulation of interleukins when IPEC-J2 were cocultured withE. colistrains this has so far never been measured in this cell line. Highest IL8 expression was found with the ETEC strain possessing the F4 fimbrium, suggesting IPEC-J2 cells to be F4 receptor positive, confirmed in a brush border membrane adhesion assay. It is concluded that the innate immune responses to pathogens and LPS makes the IPEC-J2 cell line a suitable model for research on intestinal host pathogen interaction.
机译:与人类对应物相比,IPEC-J2是一种很有前途的体外模型系统,尤其是在转录水平上没有得到很好的表征。这项研究的目的是表征与肠毒素性大肠杆菌(ETEC),非致病性大肠杆菌共孵育时IPEC-J2细胞中的基因表达。大肠杆菌和E.大肠内毒素。极化IPEC-J2单层的顶端感染导致跨上皮电阻(TEER)的时间依赖性下降。微阵列分析显示,当IPEC-J2与E共培养时,白介素上调。迄今为止,尚未在该细胞系中测量到这种菌株。在刷状缘膜粘附试验中证实,具有F4纤维的ETEC菌株发现最高的IL8表达,表明IPEC-J2细胞为F4受体阳性。结论是,对病原体和LPS的先天免疫应答使IPEC-J2细胞系成为研究肠道宿主病原体相互作用的合适模型。

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