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首页> 外文期刊>Innate immunity >Classically or alternatively activated bovine monocyte-derived macrophages in vitro do not resemble CD163/Calprotectin biased macrophage populations in the teat
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Classically or alternatively activated bovine monocyte-derived macrophages in vitro do not resemble CD163/Calprotectin biased macrophage populations in the teat

机译:体外经典或替代性激活的牛单核细胞衍生巨噬细胞与乳头中CD163 /钙卫蛋白偏向的巨噬细胞种群不相似

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摘要

The functional phenotype of resident macrophages significantly determines the character of an inflammatory response. In this study we identified two phenotypes of tissue macrophages in bovine teat tissue based on expression of Calprotectin and CD163. To investigate a possible link between the dichotomy in phenotype and functional properties of cells in association with different host mediators we set up an in vitro model with bovine monocyte-derived macrophages (MdM). In vitro differentiated MdM invariably and uniformly expressed both antigens. Classically activated MdM (IFN-γ priming and LPS stimulation) showed a decreased CD163 expression while alternative activation (IL-4/IL-13 priming) did not change expression of CD163 and Calprotectin. Differently activated MdM showed a clearly distinct expression of genes related to classical (IL-12, inducible NO synthase) or alternative activation (IL-10, arginase I). The presence of the inflammatory host mediator prostaglandin E2 (PGE2) neither influenced expression of Calprotectin and CD163 nor gene expression profiles in MdM generated in the presence of PGE2 (PGE2-MdM). Supernatants of PGE2-MdM, however, significantly dampened the migration of neutrophilic granulocytes. The results of this study highlight the discrepancy between in vivo and in vitro obtained macrophages and point to the necessity to analyze the functional capacities of bovine tissue macrophages in situ.
机译:驻留巨噬细胞的功能表型显着决定了炎症反应的特征。在这项研究中,我们根据钙卫蛋白和CD163的表达鉴定了牛乳头组织中两种组织巨噬细胞表型。为了研究表型二分法和与不同宿主介体相关的细胞功能特性之间的可能联系,我们建立了牛单核细胞衍生巨噬细胞(MdM)的体外模型。体外分化的MdM始终一致地表达两种抗原。经典激活的MdM(IFN-γ引发和LPS刺激)显示CD163表达降低,而替代激活(IL-4 / IL-13引发)不改变CD163和钙卫蛋白的表达。不同激活的MdM显示出与经典(IL-12,诱导型NO合酶)或其他激活(IL-10,精氨酸酶I)相关的基因的明显不同表达。炎症宿主介体前列腺素E2(PGE2)的存在既不影响Calprotectin和CD163的表达,也不影响在存在PGE2(PGE2-MdM)时产生的MdM中的基因表达谱。然而,PGE2-MdM的上清液显着抑制了嗜中性粒细胞的迁移。这项研究的结果突出了体内和体外获得的巨噬细胞之间的差异,并指出有必要就地分析牛组织巨噬细胞的功能能力。

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