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Description of an in vivo model for the assessment of eosinophil chemoattractants in the mouse

机译:评估小鼠嗜酸性粒细胞趋化剂的体内模型的描述

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Chemokines (chemoattractant cytokines) induce potent and selective chemotaxis of leukocyte subsets in vitro. Here, we review briefly the chemokines shown to induce eosinophil chemotaxis in vitro and describe a novel model for the study of the ability of chemokines to stimulate eosinophil migration in vivo. Eosinophils were purified from the blood of mice over-expressing the IL-5 gene and labelled with 111In. Only the C-C chemokines, eotaxin and MIP-1alpha, but not RANTES, MCP-1, MCP-3, MCP-4, MIP-1?, KC and MIP-2, effectively induced the recruitment of 111In-eosinophils in mouse skin. We suggest that this mouse model will be useful in assessing the role of endogenously-generated chemokines in mediating eosinophil migration to sites of allergic inflammation in vivo.
机译:趋化因子(趋化因子)在体外诱导白细胞亚群的有效和选择性趋化性。在这里,我们简要回顾了趋化因子在体外可诱导嗜酸性粒细胞趋化性,并描述了一种新型模型,用于研究趋化因子在体内刺激嗜酸性粒细胞迁移的能力。从过量表达IL-5基因的小鼠血液中纯化嗜酸性粒细胞,并用111In标记。只有C-C趋化因子,嗜酸性粒细胞趋化因子和MIP-1alpha,而不是RANTES,MCP-1,MCP-3,MCP-4,MIP-1α,KC和MIP-2有效诱导了111In-嗜酸性粒细胞在小鼠皮肤中的募集。我们建议,此小鼠模型将有助于评估内源性趋化因子在介导嗜酸性粒细胞迁移至体内变应性炎症部位中的作用。

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