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Altered Transcription of Murine Genes Induced in the Small Bowel by Administration of Probiotic Strain Lactobacillus rhamnosus HN001

机译:通过施用益生菌菌株鼠李糖乳杆菌HN001改变小肠中鼠基因的转录

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Lactobacillus rhamnosus HN001 is a probiotic strain reported to increase resistance to epithelium-adherent and -invasive intestinal pathogens in experimental animals. To increase understanding of the relationship between strain HN001 and the bowel, transcription of selected genes in the mucosa of the murine small bowel was measured. Mice previously naive to lactobacilli ( Lactobacillus -free mice) were examined after daily exposure to HN001 in drinking water. Comparisons were made to results from matched Lactobacillus -free mice. Infant and adult mice were investigated to provide a temporal view of gene expression in response to exposure to HN001. Genes sgk1 , angptl4 , and hspa1b , associated with the apoptosis pathway, were selected for investigation by reverse transcription-quantitative PCR on the basis of a preliminary duodenal DNA microarray screen. Normalized to gapdh gene transcription, these three genes were upregulated after 6 to 10 days exposure of adult mice to HN001. Angptl4 was shown by immunofluorescence to be upregulated in duodenal epithelial cells of mucosal samples. Epithelial cell migration was faster in HN001-exposed mice than in the Lactobacillus -free controls. Transcriptional responses in infant mice differed according to bowel region and age. For example, sgk1 was upregulated in duodenal, jejunal, and ileal mucosa of mice less than 25 days old, whereas angptl4 and hspa1b were upregulated at 10 days in the duodenum but downregulated in the jejunal mucosa until mice were 25 days old. Overall, the results provide links between a probiotic strain, mucosal gene expression, and host phenotype, which may be useful in delineating mechanisms of probiotic action.
机译:鼠李糖乳杆菌HN001是一种益生菌菌株,据报道可增加对实验动物上皮粘附和侵袭性肠道病原体的抵抗力。为了增加对菌株HN001和肠之间关系的了解,对小鼠小肠粘膜中所选基因的转录进行了测量。每天接触饮用水中的HN001后,检查以前对乳杆菌幼稚的小鼠(无乳杆菌的小鼠)。与来自匹配的无乳杆菌的小鼠的结果进行比较。对婴儿和成年小鼠进行了研究,以提供对暴露于HN001的基因表达的时间观察。在初步的十二指肠DNA微阵列筛选的基础上,选择与细胞凋亡途径相关的基因sgk1,angptl4和hspa1b进行逆转录-定量PCR研究。将成年小鼠暴露于HN001后,对gapdh基因转录进行标准化,这三个基因被上调。通过免疫荧光显示Angptl4在粘膜样品的十二指肠上皮细胞中被上调。暴露于HN001的小鼠中的上皮细胞迁移要快于无乳杆菌的对照组。婴儿小鼠的转录反应根据肠区域和年龄而有所不同。例如,在小于25天的小鼠的十二指肠,空肠和回肠粘膜中sgk1上调,而在十二指肠中的Angptl4和hspa1b在第10天上调,而在空肠粘膜中Angptl4和hspa1b在25天前下调。总的来说,该结果提供了益生菌菌株,粘膜基因表达和宿主表型之间的联系,这可能有助于描述益生菌作用的机制。

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