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吞噬作用的大鼠中性粒细胞和巨噬细胞趋化因子的差异产生

Differential production of chemokines by phagocytosing rat neutrophils and macrophages.

作者信息

al-Mokdad M, Shibata F, Takano K, Nakagawa H

机构信息

Department of Physiological Chemistry, Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University, Japan.

出版信息

Inflammation. 1998 Apr;22(2):145-59. doi: 10.1023/a:1022383922039.

Abstract

In this study, rat neutrophils and macrophages produced cytokine-induced neutrophil chemoattractants (CINCs) and rat macrophage inflammatory protein-1 alpha (MIP-1 alpha) in different patterns during phagocytosis of heat-killed yeast cells in vitro. The cultured supernatants of the phagocytosing rat neutrophils and macrophages had chemotactic activities toward neutrophils, and the chemotactic potencies were markedly inhibited by anti-CINCs IgGs or/and anti-MIP-1 alpha IgG, suggesting that CINCs and MIP-1 alpha are major neutrophil chemoattractants produced by the phagocytosing neutrophils and macrophages. Dexamethasone suppressed the production of CINCs and MIP-1 alpha by the phagocytosing cells in a dose-dependent manner. Our results demonstrate significant differences in the production of CINCs and MIP-1 alpha by neutrophils and macrophages during phagocytosis of yeast cells and thus may suggest the different contribution of each chemokine to neutrophil recruitment in the processes of inflammation in rats.

摘要

在本研究中,大鼠中性粒细胞和巨噬细胞在体外吞噬热杀死的酵母细胞过程中,以不同模式产生细胞因子诱导的中性粒细胞趋化因子(CINCs)和大鼠巨噬细胞炎性蛋白-1α(MIP-1α)。吞噬大鼠中性粒细胞和巨噬细胞的培养上清液对中性粒细胞具有趋化活性,且趋化效力被抗CINCs IgG或/和抗MIP-1α IgG显著抑制,这表明CINCs和MIP-1α是吞噬性中性粒细胞和巨噬细胞产生的主要中性粒细胞趋化因子。地塞米松以剂量依赖性方式抑制吞噬细胞产生CINCs和MIP-1α。我们的结果表明,在酵母细胞吞噬过程中,中性粒细胞和巨噬细胞产生CINCs和MIP-1α存在显著差异,因此可能提示每种趋化因子在大鼠炎症过程中对中性粒细胞募集的不同贡献。

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