[细粒棘球蚴囊液(EgCF)通过诱导细胞骨架重排抑制LPS诱导小鼠巨噬细胞的迁移和吞噬功能]。

Feiming He, Dan Dong, Yuting Chen, Yuan Liao, Ke Lin, Jin Meng, Xiangwei Wu, Xueling Chen
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引用次数: 0

摘要

目的探讨细粒棘球蚴囊液(EgCF)对脂多糖(LPS)诱导的巨噬细胞骨架重排、吞噬和迁移的影响。方法体外分离培养C57BL/6小鼠腹腔巨噬细胞,分为对照组、LPS组和LPS联合EgCF组。治疗48小时后,罗丹明标记的phalloidin染色和荧光显微镜观察丝状肌动蛋白(F-actin)的变化;TranswellTM实验室检测细胞迁移能力,流式细胞术检测细胞吞噬能力。处理1 h后,Western blot检测PI3K、AKT、磷酸化AKT (p-AKT)、Rac1、鸟苷三磷酸-Rac1 (GTP-Rac1)、WASP和Arp2蛋白的表达。结果与对照组比较,LPS刺激后巨噬细胞明显变形;伪足增多;肌动蛋白细胞骨架增加,在伪足中分布较多;迁移和吞噬能力显著提高,PI3K、p-AKT、GTP-Rac1、WASP和Arp2蛋白表达显著升高。EgCF处理导致lps活化细胞的细胞萎缩和假足突起消失,导致细胞吞噬和迁移减少;与LPS组相比,PI3K、p-AKT、GTP-Rac1、WASP、Arp2蛋白表达显著降低。结论LPS诱导巨噬细胞迁移,增强巨噬细胞的吞噬作用,而EgCF抑制巨噬细胞的迁移和吞噬作用,其作用机制与肌动蛋白细胞骨架重排有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Echinococcus granulosus cyst fluid(EgCF) inhibits the migration and phagocytic function of mouse macrophages induced by LPS via inducing cytoskeletal rearrangement].

Objective To investigate the effect of Echinococcus granulosus cyst fluid(EgCF) on the cytoskeletal rearrangement and phagocytosis and the migration of macrophages induced by lipopolysaccharide(LPS). Methods Peritoneal macrophages of C57BL/6 mice were isolated and cultured in vitro, and divided into control group and LPS group and LPS combined with EgCF group. After 48 hours of treatment, filamentous actin (F-actin) changes were observed with rhodamine-labelled phalloidin staining and fluorescence microscopy; TranswellTM chamber was used to test cell migration ability and flow cytometry to test cell phagocytosis. After 1 hour of treatment, PI3K and AKT, phosphorylated AKT (p-AKT), Rac1, guanosine triphospho-Rac1 (GTP-Rac1), WASP and Arp2 protein expressions were detected with Western blot analysis. Results Compared with the control group, after LPS stimulation, macrophages were deformed significantly; pseudopodia increased; actin cytoskeleton increased and was more distributed in pseudopodia; the ability of migration and phagocytosis were significantly improved, and the expression of PI3K, p-AKT, GTP-Rac1, WASP and Arp2 proteins significantly increased. EgCF treatment caused cell shrinkage and disappearance of pseudopodia protrusions of LPS-activated cells, and led to the reduced phagocytic and migratory of cells; the protein expression of PI3K, p-AKT, GTP-Rac1, WASP and Arp2 decreased significantly compared with the LPS group. Conclusion LPS induces the migration and enhances phagocytosis of macrophages while EgCF inhibits these effects, which is related to actin cytoskeleton rearrangement.

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