Flynn Andrew N, Buret Andre G
Department of Biological Sciences, University of Calgary, Calgary, Alberta, Canada.
Microb Pathog. 2008 Aug;45(2):98-104. doi: 10.1016/j.micpath.2007.12.004. Epub 2008 Apr 22.
The murine model of Citrobacter rodentium infection has been used to complement in vitro studies of enteropathogenic Escherichia coli (EPEC) infections of human intestinal epithelial cells (IECs). However, the differences in epithelial cell responses between these two models are not fully understood. We used an in vitro model of C. rodentium infection to examine important, yet incompletely understood, cellular responses of murine IECs to this pathogen. C. rodentium attached to CMT-93 cells and disrupted their tight junctional expression of claudins-4 and -5. This was associated with a loss of barrier function that required live bacteria and was partially prevented by the inhibition of Rho kinase. Furthermore, C. rodentium caused an upregulation of IEC apoptosis that was associated with the cytoplasmic accumulation of apoptosis-inducing factor, but not with the activation of caspase-3. These studies demonstrate for the first time that C. rodentium affects murine IECs in ways that may be similar, but distinct, to the effects of EPEC on human IECs.
啮齿柠檬酸杆菌感染的小鼠模型已被用于补充对人肠道上皮细胞(IECs)肠道致病性大肠杆菌(EPEC)感染的体外研究。然而,这两种模型之间上皮细胞反应的差异尚未完全明了。我们使用啮齿柠檬酸杆菌感染的体外模型来研究小鼠IECs对该病原体重要但尚未完全理解的细胞反应。啮齿柠檬酸杆菌附着于CMT - 93细胞并破坏了它们紧密连接蛋白claudins - 4和 - 5的表达。这与屏障功能丧失有关,这种丧失需要活细菌,并且通过抑制Rho激酶可部分预防。此外,啮齿柠檬酸杆菌导致IEC细胞凋亡上调,这与凋亡诱导因子的细胞质积累有关,但与caspase - 3的激活无关。这些研究首次证明,啮齿柠檬酸杆菌对小鼠IECs的影响方式可能与EPEC对人IECs的影响相似但不同。