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APPL endosomes are not obligatory endocytic intermediates but act as stable cargo-sorting compartments

机译:APPL内体不是强制性的胞吞中间体,而是充当稳定的货物分选区

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Endocytosis allows cargo to enter a series of specialized endosomal compartments, beginning with early endosomes harboring Rab5 and its effector EEA1. There are, however, additional structures labeled by the Rab5 effector APPL1 whose role in endocytic transport remains unclear. It has been proposed that APPL1 vesicles are transport intermediates that convert into EEA1 endosomes. Here, we tested this model by analyzing the ultrastructural morphology, kinetics of cargo transport, and stability of the APPL1 compartment over time. We found that APPL1 resides on a tubulo-vesicular compartment that is capable of sorting cargo for recycling or degradation and that displays long lifetimes, all features typical of early endosomes. Fitting mathematical models to experimental data rules out maturation of APPL1 vesicles into EEA1 endosomes as a primary mechanism for cargo transport. Our data suggest instead that APPL1 endosomes represent a distinct population of Rab5-positive sorting endosomes, thus providing important insights into the compartmental organization of the early endocytic pathway.
机译:胞吞作用使货物进入一系列专门的内体区室,从携带Rab5及其效应子EEA1的早期内体开始。但是,还存在由Rab5效应器APPL1标记的其他结构,其在胞吞转运中的作用仍不清楚。已经提出APPL1囊泡是转化为EEA1内体的转运中间体。在这里,我们通过分析超微结构形态,货物运输动力学以及APPL1舱室随时间的稳定性来测试该模型。我们发现APPL1位于肾小管囊状隔室中,该室能够分拣货物以进行回收或降解,并且使用寿命长,这是早期内体的典型特征。将数学模型拟合到实验数据可以排除将APPL1囊泡成熟到EEA1内体中作为货物运输的主要机制。我们的数据表明,APPL1内体代表了Rab5阳性分选内体的独特群体,从而为早期内吞途径的区室组织提供了重要见识。

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