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吞噬杯处膜重塑的定量分析。

Quantitative analysis of membrane remodeling at the phagocytic cup.

作者信息

Lee Warren L, Mason David, Schreiber Alan D, Grinstein Sergio

机构信息

Programme in Cell Biology, Hospital for Sick Children,Toronto, Ontario, M5G 1X8 Canada.

出版信息

Mol Biol Cell. 2007 Aug;18(8):2883-92. doi: 10.1091/mbc.e06-05-0450. Epub 2007 May 16.

Abstract

Nascent phagosomes, which are derived from the plasma membrane, acquire microbicidal properties through multiple fusion and fission events collectively known as maturation. Here we show that remodeling of the phagosomal membrane is apparent even before sealing, particularly when large particles are ingested. Fluorescent probes targeted to the plasma membrane are cleared from the region lining the particle before engulfment is completed. Extensive clearance was noted for components of the inner as well as outer monolayer of the plasmalemma. Segregation of lipid microdomains was ruled out as the mechanism underlying membrane remodeling, because markers residing in rafts and those that are excluded were similarly depleted. Selective endocytosis was also ruled out. Instead, several lines of evidence indicate that endomembranes inserted by exocytosis at sites of ingestion displace the original membrane constituents from the base of the phagosomal cup. The Fcgamma receptors that trigger phagocytosis remain associated with their ligands. By contrast, Src-family kinases that are the immediate effectors of receptor activation are flushed away from the cup by the incoming membranes. Together with the depletion of phosphoinositides required for signal transduction, the disengagement of receptors from their effectors by bulk membrane remodeling provides a novel means to terminate receptor signaling.

摘要

新生吞噬体源自质膜,通过一系列统称为成熟的融合和裂变事件获得杀菌特性。我们在此表明,吞噬体膜的重塑在封闭之前就已明显,尤其是在吞噬大颗粒时。在吞噬完成之前,靶向质膜的荧光探针就已从颗粒周围区域清除。质膜内、外单层的成分都有大量清除。脂质微区的分离被排除为膜重塑的潜在机制,因为存在于脂筏中的标记物和那些被排除在外的标记物同样被耗尽。选择性内吞作用也被排除。相反,几条证据表明,通过胞吐作用在吞噬部位插入的内膜将原始膜成分从吞噬杯底部取代。触发吞噬作用的Fcγ受体仍与其配体结合。相比之下,作为受体激活直接效应器的Src家族激酶被进入的膜从吞噬杯中冲走。连同信号转导所需的磷酸肌醇的耗尽,通过大量膜重塑使受体与其效应器分离提供了一种终止受体信号传导的新方法。

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