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雪貂淋巴管内皮细胞的分离、鉴定及功能分析。

Isolation, characterization, and functional analysis of ferret lymphatic endothelial cells.

作者信息

Berendam Stella J, Fallert Junecko Beth A, Murphey-Corb Michael A, Fuller Deborah H, Reinhart Todd A

机构信息

Department of Infectious Diseases and Microbiology, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA 15261, USA.

Department of Microbiology and Molecular Genetics, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15261, USA.

出版信息

Vet Immunol Immunopathol. 2015 Feb 15;163(3-4):134-45. doi: 10.1016/j.vetimm.2014.11.013. Epub 2014 Dec 3.

Abstract

The lymphatic endothelium (LE) serves as a conduit for transport of immune cells and soluble antigens from peripheral tissues to draining lymph nodes (LNs), contributing to development of host immune responses and possibly dissemination of microbes. Lymphatic endothelial cells (LECs) are major constituents of the lymphatic endothelium. These specialized cells could play important roles in initiation of host innate immune responses through sensing of pathogen-associated molecular patterns (PAMPs) by pattern recognition receptors (PRRs), including toll-like receptors (TLRs). LECs secrete pro-inflammatory cytokines and chemokines to create local inflammatory conditions for recruitment of naïve antigen presenting cells (APCs) such as dendritic cells (DCs) to sites of infection and/or vaccine administration. In this study, we examined the innate immune potential of primary LEC populations derived from multiple tissues of an animal model for human infectious diseases - the ferret. We generated a total of six primary LEC populations from lung, tracheal, and mesenteric LN tissues from three different ferrets. Standard RT-PCR characterization of these primary LECs showed that they varied in their expression of LEC markers. The ferret LECs were examined for their ability to respond to poly I:C (TLR3 and RIG-I ligand) and other known TLR ligands as measured by production of proinflammatory cytokine (IFNα, IL6, IL10, Mx1, and TNFα) and chemokine (CCL5, CCL20, and CXCL10) mRNAs using real time RT-PCR. Poly I:C exposure induced robust proinflammatory responses by all of the primary ferret LECs. Chemotaxis was performed to determine the functional activity of CCL20 produced by the primary lung LECs and showed that the LEC-derived CCL20 was abundant and functional. Taken together, our results continue to reveal the innate immune potential of primary LECs during pathogen-host interactions and expand our understanding of the roles LECs might play in health and disease in animal models.

摘要

淋巴内皮(LE)作为免疫细胞和可溶性抗原从外周组织运输至引流淋巴结(LN)的通道,有助于宿主免疫反应的发展,并可能促进微生物的传播。淋巴内皮细胞(LEC)是淋巴内皮的主要组成部分。这些特殊细胞可通过模式识别受体(PRR),包括Toll样受体(TLR)感知病原体相关分子模式(PAMP),从而在宿主固有免疫反应的启动中发挥重要作用。LEC分泌促炎细胞因子和趋化因子,为幼稚抗原呈递细胞(APC),如树突状细胞(DC)募集到感染部位和/或疫苗接种部位创造局部炎症条件。在本研究中,我们检测了源自人类传染病动物模型——雪貂多个组织的原代LEC群体的固有免疫潜能。我们从三只不同雪貂的肺、气管和肠系膜淋巴结组织中总共生成了六个原代LEC群体。对这些原代LEC进行的标准逆转录聚合酶链反应(RT-PCR)表征显示,它们在LEC标志物的表达上存在差异。通过实时RT-PCR检测促炎细胞因子(IFNα、IL6、IL10、Mx1和TNFα)和趋化因子(CCL5、CCL20和CXCL10)mRNA的产生,检测雪貂LEC对聚肌胞苷酸(poly I:C,TLR3和RIG-I配体)及其他已知TLR配体的反应能力。poly I:C刺激可诱导所有原代雪貂LEC产生强烈的促炎反应。进行趋化性实验以确定原代肺LEC产生的CCL20的功能活性,结果表明LEC来源 的CCL20含量丰富且具有功能。综上所述,我们的结果不断揭示原代LEC在病原体与宿主相互作用过程中的固有免疫潜能,并扩展了我们对LEC在动物模型的健康和疾病中可能发挥作用的理解。

相似文献

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Isolation, characterization, and functional analysis of ferret lymphatic endothelial cells.雪貂淋巴管内皮细胞的分离、鉴定及功能分析。
Vet Immunol Immunopathol. 2015 Feb 15;163(3-4):134-45. doi: 10.1016/j.vetimm.2014.11.013. Epub 2014 Dec 3.

本文引用的文献

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Culturing purifies murine lymph node lymphatic endothelium.培养可纯化小鼠淋巴结淋巴管内皮细胞。
Lymphat Res Biol. 2014 Sep;12(3):144-9. doi: 10.1089/lrb.2013.0053. Epub 2014 May 16.
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Viral infection of the lung: host response and sequelae.肺部病毒感染:宿主反应和后遗症。
J Allergy Clin Immunol. 2013 Dec;132(6):1263-76; quiz 1277. doi: 10.1016/j.jaci.2013.06.006. Epub 2013 Aug 1.

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