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小鼠巨噬细胞对炭疽杆菌水肿毒素的转录和功能反应。

Murine macrophage transcriptional and functional responses to Bacillus anthracis edema toxin.

作者信息

Comer Jason E, Galindo Cristi L, Zhang Fan, Wenglikowski Autumn M, Bush Katie L, Garner Harold R, Peterson Johnny W, Chopra Ashok K

机构信息

Department of Microbiology and Immunology, The University of Texas Medical Branch, Galveston, TX 77555-1070, USA.

出版信息

Microb Pathog. 2006 Aug-Sep;41(2-3):96-110. doi: 10.1016/j.micpath.2006.05.001. Epub 2006 Jul 18.

Abstract

Edema toxin (EdTx), which is a combination of edema factor and a binding moiety (protective antigen), is produced by Bacillus anthracis, the etiological agent of anthrax. EdTx is an adenylyl cyclase enzyme that converts adenosine triphosphate to adenosine-3',5'-monophosphate, resulting in interstitial edema seen in anthrax patients. We used GeneChip analysis to examine global transcriptional profiles of EdTx-treated RAW 264.7 murine macrophage-like cells and identified 71 and 259 genes whose expression was significantly altered by the toxin at 3 and 6h, respectively. Alteration in the expression levels of selected genes was confirmed by real time-reverse transcriptase polymerase chain reaction. The genes with up-regulated expression in macrophages in response to EdTx-treatment were known to be involved in inflammatory responses, regulation of apoptosis, adhesion, immune cell activation, and transcription regulation. Additionally, GeneChip analysis results implied that EdTx-induced activation of activator protein-1 (AP-1) and CAAAT/enhancer-binding protein-beta (C/EBP-beta). Gel shift assays were therefore performed, and an increase in the activities of both of these transcription factors was observed within 30 min. EdTx also inhibited tumor necrosis factor alpha production and crippled the phagocytic ability of the macrophages. This is the first report detailing the host cell global transcriptional responses to EdTx.

摘要

水肿毒素(EdTx)是水肿因子和一个结合部分(保护性抗原)的组合,由炭疽病的病原体炭疽芽孢杆菌产生。EdTx是一种腺苷酸环化酶,可将三磷酸腺苷转化为3',5'-环磷酸腺苷,导致炭疽患者出现间质水肿。我们使用基因芯片分析来检测经EdTx处理的RAW 264.7鼠巨噬细胞样细胞的整体转录谱,并分别鉴定出71个和259个基因,其表达在3小时和6小时时被该毒素显著改变。通过实时逆转录聚合酶链反应证实了所选基因表达水平的改变。已知经EdTx处理后巨噬细胞中表达上调的基因参与炎症反应、细胞凋亡调节、黏附、免疫细胞激活和转录调节。此外,基因芯片分析结果表明EdTx诱导激活蛋白-1(AP-1)和CCAAT/增强子结合蛋白-β(C/EBP-β)。因此进行了凝胶迁移试验,在30分钟内观察到这两种转录因子的活性均增加。EdTx还抑制肿瘤坏死因子α的产生,并削弱巨噬细胞的吞噬能力。这是第一份详细描述宿主细胞对EdTx的整体转录反应的报告。

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