Suppr超能文献

用金黄色葡萄球菌的脂磷壁酸加肽聚糖刺激的牛乳腺上皮细胞的基因表达谱分析

Gene expression profiling of bovine mammary gland epithelial cells stimulated with lipoteichoic acid plus peptidoglycan from Staphylococcus aureus.

作者信息

Im Jintaek, Lee Taeheon, Jeon Jun Ho, Baik Jung Eun, Kim Kyoung Whun, Kang Seok-Seong, Yun Cheol-Heui, Kim Heebal, Han Seung Hyun

机构信息

Department of Oral Microbiology and Immunology, DRI, and BK21 Plus Program, School of Dentistry, Seoul National University, Seoul 110-749, Republic of Korea.

Department of Agricultural Biotechnology and Research Institute for Agriculture and Life Sciences, Seoul National University, Seoul 151-921, Republic of Korea.

出版信息

Int Immunopharmacol. 2014 Jul;21(1):231-40. doi: 10.1016/j.intimp.2014.05.002. Epub 2014 May 14.

Abstract

A Gram-positive bacterium, Staphylococcus aureus is known to be one of the major pathogenic bacteria responsible for causing bovine mastitis. Among the various cell wall components of S. aureus, lipoteichoic acid (LTA) and peptidoglycan (PGN) are closely associated with inflammatory responses. However, the role of LTA and PGN derived from S. aureus in bovine mastitis has not been clearly elucidated. In this study, we characterized the gene expression profile of a bovine mammary gland epithelial cell line, MAC-T cells, in the presence of LTA and PGN from S. aureus. LTA plus PGN, but not LTA or PGN alone, activated MAC-T cells. The analysis of transcriptional profiles using an Affymetrix genechip microarray showed that stimulation with LTA plus PGN produced a total of 2019 (fold change >1.2) differentially expressed genes (DEGs), with 801 up-regulated genes and 1218 down-regulated genes. Of the up-regulated genes, 14 inflammatory mediator-related DEGs, 22 intra-cellular signaling molecule-related DEGs, and 15 transcription factor-related DEGs were observed, whereas among the down-regulated DEGs 17 inflammation-related DEGs were found. The microarray results were confirmed using real-time RT-PCR of 18 genes with substantial changes in expression (9 each from the up-regulated and down-regulated DEGs). These results provide a comprehensive analysis of gene-expression profiles elicited by S. aureus LTA and PGN in MAC-T cells, contributing to an understanding of the pathogenesis for S. aureus-induced bovine mastitis.

摘要

金黄色葡萄球菌是一种革兰氏阳性菌,已知是引起牛乳腺炎的主要病原菌之一。在金黄色葡萄球菌的各种细胞壁成分中,脂磷壁酸(LTA)和肽聚糖(PGN)与炎症反应密切相关。然而,源自金黄色葡萄球菌的LTA和PGN在牛乳腺炎中的作用尚未得到明确阐明。在本研究中,我们对牛乳腺上皮细胞系MAC-T细胞在存在来自金黄色葡萄球菌的LTA和PGN的情况下的基因表达谱进行了表征。LTA加PGN可激活MAC-T细胞,但单独的LTA或PGN则不能。使用Affymetrix基因芯片微阵列对转录谱进行分析表明,用LTA加PGN刺激产生了总共2019个(倍数变化>1.2)差异表达基因(DEG),其中801个基因上调,1218个基因下调。在上调的基因中,观察到14个与炎症介质相关的DEG、22个与细胞内信号分子相关的DEG和15个与转录因子相关的DEG,而在下调的DEG中发现了17个与炎症相关的DEG。使用实时RT-PCR对18个表达有显著变化的基因(上调和下调的DEG各9个)对微阵列结果进行了验证。这些结果提供了对金黄色葡萄球菌LTA和PGN在MAC-T细胞中引发的基因表达谱的全面分析,有助于理解金黄色葡萄球菌诱导的牛乳腺炎的发病机制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验