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首页> 外文期刊>Philosophical Transactions of the Royal Society of London, Series B. Biological Sciences >Rab8a localisation and activation by Toll-like receptors on macrophage macropinosomes
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Rab8a localisation and activation by Toll-like receptors on macrophage macropinosomes

机译:Rab8a在巨噬细胞癌细胞上的造成roll样受体的定位和活化

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摘要

Macropinocytosis is a prevalent and essential pathway inmacrophages where it contributes to anti-microbial responses and innate immune cell functions. Cell surface ruffles give rise to phagosomes and to macropinosomes as multi-functional compartments that contribute to environmental sampling, pathogen entry, plasma membrane turnover and receptor signalling. Rapid, high resolution, lattice light sheet imaging demonstrates the dynamic nature of macrophage ruffling. Pathogen-mediated activation of surface and endosomal Toll-like receptors (TLRs) in macrophages upregulates macropinocytosis. Here, using multiple forms of imaging and microscopy, we track membrane-associated, fluorescently-tagged Rab8a expressed in live macrophages, using a variety of cell markers to demonstrate Rab8a localization and its enrichment on early macropinosomes. Production of a novel biosensor and its use for quantitative FRET analysis in live cells, pinpoints macropinosomes as the site for TLR-induced activation of Rab8a. We have previously shown that TLR signalling, cytokine outputs and macrophage programming are regulated by the GTPase Rab8a with PI3 K gamma as its effector. Finally, we highlight another effector, the phosphatase OCRL, which is located on macropinosomes and interacts with Rab8a, suggesting that Rab8a may operate on multiple levels to modulate phosphoinositides in macropinosomes. These findings extend our understanding of macropinosomes as regulatory compartments for innate immune function in macrophages.
机译:Macropinocytosis是一种普遍的和必需的途径,其有助于抗微生物反应和先天免疫细胞功能。细胞表面褶皱导致吞噬物质和大批体作为多功能隔室,其有助于环境采样,病原体进入,质膜周转和受体信号传导。快速,高分辨率,格式光板成像展示了巨噬细胞荷丝的动态性质。病原体介导的表面和内体性收缩受体(TLR)在巨噬细胞中的激活上调癌细胞症。这里,使用多种形式的成像和显微镜,我们跟踪在活巨噬细胞中表达的膜相关的荧光标记的Rab8a,使用各种细胞标记物证明Rab8a定位及其在早期的宏观体内的富集。生产新型生物传感器及其用于活细胞的定量褶皱分析,针对TLR诱导的Rab8a激活的Macropinosomes。我们之前已经表明,TLR信令,细胞因子输出和巨噬细胞编程由GTP酶Rab8a调节,用PI3kγ作为其效应器。最后,我们突出了另一种效应器,磷酸酶OCR1位于大甲基体上并与Rab8a相互作用,表明Rab8a可以在多水平上运行以调节大麦多组中的磷膦酸性。这些发现将我们对Macroposomes的理解扩展为巨噬细胞内未经免疫功能的监管隔间。

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