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猪Toll样受体3(TLR3)的特性及其在应对流感病毒和支气管败血波氏杆菌时的表达

Porcine TLR3 characterization and expression in response to influenza virus and Bordetella bronchiseptica.

作者信息

Sacco Randy E, Nicholson Tracy L, Waters Theresa E, Brockmeier Susan L

机构信息

National Animal Disease Center, USDA/ARS, Ames, IA 50010, USA.

出版信息

Vet Immunol Immunopathol. 2011 Jul 15;142(1-2):57-63. doi: 10.1016/j.vetimm.2011.04.008. Epub 2011 Apr 20.

Abstract

We have provided a detailed structural analysis of porcine alveolar macrophage TLR3 extracellular domain (ECD). The porcine TLR3-ECD contains 18 leucine-rich repeats (LRRs) consisting of blocks of consensus motifs and non-consensus motifs containing insertions. Excluding the N-terminal and C-terminal LRRs, porcine TLR3 has two LRRs with insertions, resulting in one LRR of 39 amino acids and another LRR of 34 amino acids. Furthermore, we have conducted the first examination of the regulated expression of porcine alveolar macrophage TLR3 during in vivo co-infection with influenza virus and Bordetella bronchiseptica. There was a bi-phasic upregulation of porcine TLR3 during influenza virus infection (day 1 and day 10 post-infection). Co-infection resulted in an enhanced expression of porcine TLR3 only at day 1 post-infection. Interestingly, B. bronchiseptica induced an upregulation in alveolar macrophage TLR3 expression at day 10 post-infection. Based on our work and that of others, TLR3 likely plays a key role in the immune response of lung cells to influenza virus infection in several mammalian species.

摘要

我们已经对猪肺泡巨噬细胞Toll样受体3(TLR3)胞外结构域(ECD)进行了详细的结构分析。猪TLR3-ECD包含18个富含亮氨酸的重复序列(LRR),由共有基序和含有插入序列的非共有基序组成。除去N端和C端的LRR,猪TLR3有两个带有插入序列的LRR,分别形成一个39个氨基酸的LRR和另一个34个氨基酸的LRR。此外,我们首次检测了猪肺泡巨噬细胞TLR3在流感病毒和支气管败血波氏杆菌体内共感染过程中的表达调控情况。在流感病毒感染期间(感染后第1天和第10天),猪TLR3出现双相上调。共感染仅在感染后第1天导致猪TLR3表达增强。有趣的是,支气管败血波氏杆菌在感染后第10天诱导肺泡巨噬细胞TLR3表达上调。基于我们和其他人的研究工作,TLR3可能在几种哺乳动物的肺细胞对流感病毒感染的免疫反应中起关键作用。

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