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1型和2型细胞因子对巨噬细胞内吞作用的调节:与干扰素-γ或白细胞介素-10相反,白细胞介素-4/白细胞介素-13的差异激活作用

Type 1 and type 2 cytokine regulation of macrophage endocytosis: differential activation by IL-4/IL-13 as opposed to IFN-gamma or IL-10.

作者信息

Montaner L J, da Silva R P, Sun J, Sutterwala S, Hollinshead M, Vaux D, Gordon S

机构信息

The Wistar Institute, Philadelphia, PA 19104, USA.

出版信息

J Immunol. 1999 Apr 15;162(8):4606-13.

Abstract

Cytokine regulation of endocytic activity in primary human macrophages was studied to define ultrastructural changes and mechanisms of pinocytic regulation associated with cytokines secreted by activated T cells. The effects of IFN-gamma (type 1) and IL-4/IL-13 and IL-10 (type 2) cytokines on fluid phase and mannose receptor-mediated endocytosis were assessed by horseradish peroxidase and colloidal gold-BSA uptake and computer-assisted morphometric analysis. IL-4 and IL-13 enhanced fluid phase pinocytosis and mannose receptor-mediated uptake by activation of phosphatidylinositol 3-kinase. Inhibition of actin assembly showed that both cytokines exerted actin-dependent and -independent effects. Ultrastructurally, IL-4 and IL-13 increased tubular vesicle formation underneath the plasma membrane and at pericentriolar sites, concurrent with decreased particle sorting to lysosomes. By contrast, IL-10 or IFN-gamma decreased both fluid phase pinocytosis and mannose receptor-mediated uptake. IFN-gamma stimulated increased particle sorting to perinuclear lysosomes, while IL-10 decreased this activity. In summary, our data document differential effects on macrophage endocytic functions by type 1 or type 2 cytokines associated with induction and effector pathways in immunity.

摘要

研究了细胞因子对原代人巨噬细胞内吞活性的调节作用,以确定与活化T细胞分泌的细胞因子相关的超微结构变化和胞饮调节机制。通过辣根过氧化物酶和胶体金-BSA摄取以及计算机辅助形态计量分析,评估了IFN-γ(1型)、IL-4/IL-13和IL-10(2型)细胞因子对液相和甘露糖受体介导的内吞作用的影响。IL-4和IL-13通过激活磷脂酰肌醇3-激酶增强了液相胞饮作用和甘露糖受体介导的摄取。肌动蛋白组装的抑制表明,这两种细胞因子都发挥了肌动蛋白依赖性和非依赖性作用。超微结构上,IL-4和IL-13增加了质膜下方和中心粒周围部位的管状囊泡形成,同时减少了向溶酶体的颗粒分选。相比之下,IL-10或IFN-γ降低了液相胞饮作用和甘露糖受体介导的摄取。IFN-γ刺激增加了向核周溶酶体的颗粒分选,而IL-10降低了这种活性。总之,我们的数据记录了1型或2型细胞因子对巨噬细胞内吞功能的不同影响,这些影响与免疫中的诱导和效应途径相关。

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