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干扰素和白细胞介素-4对猪巨噬细胞的表型和功能调节

Phenotypic and functional modulations of porcine macrophages by interferons and interleukin-4.

作者信息

Sautter Carmen A, Auray Gaël, Python Sylvie, Liniger Matthias, Summerfield Artur

机构信息

Institute of Virology and Immunology IVI, Sensemattstrasse 293, 3147, Mittelhäusern, Switzerland; Graduate School for Cellular and Biomedical Sciences, University of Bern, Freiestrasse 1, 3012, Bern, Switzerland; Department of Infectious Diseases and Pathobiology (DIP), Vetsuisse Faculty, University of Bern, Länggassstrasse 122, 3012, Bern, Switzerland.

Institute of Virology and Immunology IVI, Sensemattstrasse 293, 3147, Mittelhäusern, Switzerland.

出版信息

Dev Comp Immunol. 2018 Jul;84:181-192. doi: 10.1016/j.dci.2018.01.018. Epub 2018 Jan 31.

Abstract

Considering that macrophage functions are strongly impacted by the local tissue environment and the type of immune response, the aim of this study was to carefully set the methodological baseline for phenotype and functions of polarized porcine monocyte-derived macrophages. To this end, macrophages were generated in autologous serum alone or with colony-stimulating factor (CSF)-1 or CSF-2, and subsequently polarized with interferon (IFN)γ, interleukin-4 or IFNβ. IFNγ promoted expression of MHC class I, MHC class II, CD11a, and CD40 as well as LPS-induced IL-6 and IL-12. A hallmark of interleukin-4 was Arginase 1 and CD203a upregulation, without abrogating pro-inflammatory cytokine production. IFNβ induced CD169, MHC class I, CD40, CD80/86, but suppressed IL-6, IL-12 and tumor-necrosis-factor secretion. CSF-2 alone altered macrophage differentiation and promoted an IFNγ-like polarization. Altogether, the results provide a comprehensive overview of porcine macrophage polarization, and demonstrate commonalities with other species as well as peculiarities of the pig.

摘要

鉴于巨噬细胞功能受到局部组织环境和免疫反应类型的强烈影响,本研究的目的是仔细设定极化猪单核细胞衍生巨噬细胞表型和功能的方法学基线。为此,巨噬细胞在单独的自体血清中或与集落刺激因子(CSF)-1或CSF-2一起生成,随后用干扰素(IFN)γ、白细胞介素-4或IFNβ进行极化。IFNγ促进了MHC I类、MHC II类、CD11a和CD40的表达以及脂多糖诱导的IL-6和IL-12的表达。白细胞介素-4的一个标志是精氨酸酶1和CD203a上调,而不消除促炎细胞因子的产生。IFNβ诱导CD169、MHC I类、CD40、CD80/86,但抑制IL-6、IL-12和肿瘤坏死因子的分泌。单独的CSF-2改变了巨噬细胞的分化并促进了类似IFNγ的极化。总之,这些结果提供了猪巨噬细胞极化的全面概述,并证明了与其他物种的共性以及猪的独特性。

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