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CD154作为活性葡萄球菌肠毒素A快速定量分析的潜在早期分子生物标志物。

CD154 as a potential early molecular biomarker for rapid quantification analysis of active Staphylococcus enterotoxin A.

作者信息

Rasooly Reuven, Hernlem Bradley J

机构信息

Western Regional Research Center, Agricultural Research Service, U.S. Department of Agriculture, Albany, CA 94710, USA.

出版信息

FEMS Immunol Med Microbiol. 2012 Mar;64(2):169-74. doi: 10.1111/j.1574-695X.2011.00874.x.

Abstract

Staphylococcus aureus is a major bacterial pathogen producing a group of 21 enterotoxins (SEs). These enterotoxins have two separate but related biological activities. They cause gastroenteritis, and they function as superantigens that activate large numbers of T cells. In the current study, we demonstrate that short-term ex vivo exposure of primary naïve CD4(+) T-cells to SEA induces differential expression of the T cell surface receptor CD154 in a time- and dose-dependent manner. In addition, we show that SEA induces higher CD154 protein expression and higher splenocyte cell proliferation compared with SEB. We also demonstrate that expression of CD154 can be used for rapid detection of active SEA in milk.

摘要

金黄色葡萄球菌是一种主要的细菌病原体,可产生一组21种肠毒素(SEs)。这些肠毒素具有两种独立但相关的生物学活性。它们会引起肠胃炎,并且作为超抗原发挥作用,激活大量T细胞。在本研究中,我们证明,将原代初始CD4(+) T细胞短期离体暴露于SEA会以时间和剂量依赖性方式诱导T细胞表面受体CD154的差异表达。此外,我们表明,与SEB相比,SEA诱导更高的CD154蛋白表达和更高的脾细胞增殖。我们还证明,CD154的表达可用于快速检测牛奶中的活性SEA。

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