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首页> 外文期刊>The Veterinary Journal >Microarray analysis of differential expression of cell cycle and cell differentiation genes in cells infected with Lawsonia intracellularis
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Microarray analysis of differential expression of cell cycle and cell differentiation genes in cells infected with Lawsonia intracellularis

机译:胞内劳森氏菌感染细胞中细胞周期和细胞分化基因差异表达的微阵列分析

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摘要

Infection of intestinal crypt epithelial cells by the obligate intracellular bacterium Lawsonia intracellularis is directly linked to marked proliferation of the infected enterocytes within 3-5 days post-infection. The virulence factor for this unique host cell-proliferative response is not known, but is considered to involve altered crypt cell cycle or differentiation events. McCoy mouse fibroblast cells were infected with L. intracellularis, and then harvested for expressed mRNA at daily time points, with matching non-infected control cell cultures. Mouse DNA microarray (>44,000 transcript targets) analysis of cDNA derived from matching mRNA samples showed over 40 identifiable genes with at least 4-fold changes between days 0 and 3 after infection with L. intracellularis. These included altered transcription of typical host cell 'alarm' response genes, such as interferon-related response genes Isgf3g and Igtp, known to be associated with invading microbial agents. Altered transcription of several genes in these cells known to be active in regulation of the cell cycle or cell differentiation genes, including usp18, Hr, Elavl2 and Slfn2, were also detected. The altered transcription of several of these genes via RT-PCR analysis was confirmed. The microarray-detected altered transcription of cell cycle and cell differentiation genes is of possible interest for links to Lawsonia-related disturbances in epithelial cell differentiation within the intestinal crypt, but this would need to be confirmed in intestinal epithelial cell studies.
机译:专性细胞内细菌胞内劳森菌对肠道隐窝上皮细胞的感染与感染后3-5天内感染的肠上皮细胞的明显增殖直接相关。这种独特的宿主细胞增殖反应的毒力因子尚不清楚,但被认为涉及改变的隐窝细胞周期或分化事件。 McCoy小鼠成纤维细胞被细胞内劳森氏菌感染,然后在每天的某个时间点收获其表达的mRNA,并带有匹配的未感染对照细胞培养物。小鼠DNA微阵列(> 44,000个转录物靶标)对来自匹配mRNA样本的cDNA的分析显示,超过40种可识别的基因在感染细胞内劳森氏菌后的第0天到第3天之间至少发生了4倍的变化。这些包括改变了典型宿主细胞“警报”反应基因的转录,例如已知与入侵微生物有关的干扰素相关反应基因Isgf3g和Igtp。这些细胞中已知对调节细胞周期或细胞分化基因有活性的几个基因的转录也发生了改变,包括usp18,Hr,Elavl2和Slfn2。通过RT-PCR分析证实了其中一些基因的转录改变。微阵列检测到的细胞周期和细胞分化基因转录的改变可能与肠隐窝内上皮细胞分化中劳森菌相关的紊乱有关,但是这需要在肠上皮细胞研究中得到证实。

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