Activation of macrophage complement receptors for phagocytosis.

F M Griffin
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引用次数: 18

Abstract

Macrophage complement receptors, while innately incapable of promoting phagocytosis, can be activated to do so by a number of inflammatory stimuli and by several immunologic mechanisms. Studies with a complement receptor-activating lymphokine reveal that activation occurs as a result of mobilization of innately immobile receptors and suggest that receptor mobility is a prerequisite for phagocytosis. Since Fc receptors are susceptible to blockade by immune complexes at inflammatory sites, phagocytosis mediated by macrophage complement receptors may be of prime importance in vivo.

巨噬细胞补体受体对吞噬作用的激活。
巨噬细胞补体受体虽然天生不能促进吞噬,但可以通过一些炎症刺激和几种免疫机制激活。补体受体激活淋巴因子的研究表明,激活是先天不动受体动员的结果,并表明受体的移动是吞噬的先决条件。由于Fc受体容易被炎症部位的免疫复合物阻断,巨噬细胞补体受体介导的吞噬作用在体内可能是最重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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