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首页> 外文期刊>Microscopy >Transient recruitment of M-Ras GTPase to phagocytic cups in RAW264 macrophages during Fc gamma R-mediated phagocytosis
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Transient recruitment of M-Ras GTPase to phagocytic cups in RAW264 macrophages during Fc gamma R-mediated phagocytosis

机译:FCγr型肾癌吞噬作用期间Raw264巨噬细胞M-RAS GTP酶对吞噬杯的泌尿病

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摘要

M-Ras, a member of the Ras superfamily, is known to be involved in diverse cellular processes. However, its involvement in Fc gamma mediated phagocytosis remains unknown. We examined the spatiotemporal localization of M-Ras during the engulfment of IgG-opsonized erythrocytes (IgG-Es) in RAW264 macrophages. By the live-cell imaging of fluorescent protein-fused M-Ras, we found that M-Ras was localized to the membrane of phagocytic cups during the early stage of phagosome formation. Notably, ratiometric image analysis revealed that M-Ras was concentrated in the membrane of forming phagosomes. Moreover, our analysis of M-Ras mutant expression showed that phagosome formation was significantly inhibited in cells expressing GDP-locked mutant M-Ras-S27N. In contrast, the expression of wild-type M-Ras or GTP-locked mutant M-Ras-G22V facilitated the uptake of IgG-Es. These data suggest that M-Ras is a novel component of the Fc gamma R-mediated phagocytic pathway and may regulate phagosome formation in macrophages.
机译:Ras Superfamily的成员M-Ras被称为不同的细胞过程。然而,其参与Fcγ介导的吞噬作用仍然未知。我们在Raw264巨噬细胞中吞噬IgG opsonized红细胞(IgG-ES)吞噬过程中M-RAS的时空定位。通过荧光蛋白熔融M-RA的活细胞成像,我们发现在吞噬蛋白酶体的早期阶段,M-RA被定位于吞噬杯的膜。值得注意的是,比率图像分析显示,在形成吞噬体的膜中浓缩M-RA。此外,我们对M-RAS突变体表达的分析表明,在表达GDP锁定突变体M-RAS-S27N的细胞中显着抑制了吞噬体形成。相反,野生型M-Ras或GTP锁定突变体M-RAS-G22V的表达促进了IgG-ES的摄取。这些数据表明M-RAS是FCγR介导的吞噬途径的新组分,可以调节巨噬细胞的吞噬组形成。

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