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感染细胞内罗森尼亚菌的猪体内细胞转运和黏膜完整性维持相关机制的下调。

Down-regulation of mechanisms involved in cell transport and maintenance of mucosal integrity in pigs infected with Lawsonia intracellularis.

机构信息

The Roslin Institute, University of Edinburgh, Easter Bush Campus, Roslin, Midlothian EH25 9RG, UK.

出版信息

Vet Res. 2014 May 20;45(1):55. doi: 10.1186/1297-9716-45-55.

Abstract

Lawsonia intracellularis is an obligate intracellular bacterium, responsible for the disease complex known as proliferative enteropathy (PE). L. intracellularis is associated with intestinal crypt epithelial cell proliferation but the mechanisms responsible are yet to be defined. Microarray analysis was used to investigate the host-pathogen interaction in experimentally infected pigs to identify pathways that may be involved. Ileal samples originating from twenty-eight weaner pigs experimentally challenged with a pure culture of L. intracellularis (strain LR189/5/83) were subjected to microarray analysis. Microarray transcriptional signatures were validated using immunohistochemistry and quantitative real time PCR of selected genes at various time points post challenge. At peak of infection (14 days post challenge) 86% of altered transcripts were down regulated, particularly those involved in maintenance of mucosal integrity and regulation of cell transport. Among the up-regulated transcripts, CD163 and CDK1 were novel findings and considered to be important, due to their respective roles in innate immunity and cellular proliferation. Overall, targeted cellular mechanisms included those that are important in epithelial restitution, migration and protection; maintenance of stable inter-epithelial cell relationships; cell transport of nutrients and electrolytes; innate immunity; and cell cycle.

摘要

内罗毕分枝杆菌是一种专性细胞内细菌,可引发增殖性肠病(PE)。内罗毕分枝杆菌与肠隐窝上皮细胞增殖有关,但具体机制尚未确定。本研究采用微阵列分析,研究了实验感染猪中的宿主-病原体相互作用,以确定可能参与的途径。对 28 头实验感染内罗毕分枝杆菌(LR189/5/83 株)的仔猪的回肠样本进行了微阵列分析。使用免疫组织化学和定量实时 PCR 技术对选定基因在感染后不同时间点的转录谱进行了验证。在感染高峰期(感染后 14 天),86%的转录本下调,特别是与黏膜完整性维持和细胞转运调节相关的基因。在上调的转录本中,CD163 和 CDK1 是新发现的,由于它们分别在先天免疫和细胞增殖中的作用而被认为很重要。总之,靶向细胞机制包括在上皮修复、迁移和保护、稳定的细胞间关系维持、营养和电解质的细胞转运、先天免疫和细胞周期中发挥重要作用的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd98/4031155/fc4d5083bd27/1297-9716-45-55-1.jpg

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