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果蝇中JAK/STAT信号通路的内吞作用调控

The endocytic control of JAK/STAT signalling in Drosophila.

作者信息

Devergne Olivier, Ghiglione Christian, Noselli Stéphane

机构信息

Institute of Developmental Biology and Cancer, CNRS-UMR 6543, University of Nice Sophia-Antipolis, Parc Valrose 06108 Nice cedex 2, France.

出版信息

J Cell Sci. 2007 Oct 1;120(Pt 19):3457-64. doi: 10.1242/jcs.005926. Epub 2007 Sep 12.

Abstract

Domeless (Dome) is an IL-6-related cytokine receptor that activates a conserved JAK/STAT signalling pathway during Drosophila development. Despite good knowledge of the signal transduction pathway in several models, the role of receptor endocytosis in JAK/STAT activation remains poorly understood. Using both in vivo genetic analysis and cell culture assays, we show that ligand binding of Unpaired 1 (Upd1) induces clathrin-dependent endocytosis of receptor-ligand complexes and their subsequent trafficking through the endosomal compartment towards the lysosome. Surprisingly, blocking trafficking in distinct endosomal compartments using mutants affecting either Clathrin heavy chain, rab5, Hrs or deep orange led to an inhibition of the JAK/STAT pathway, whereas this pathway was unchanged when rab11 was affected. This suggests that internalization and trafficking are both required for JAK/STAT activity. The requirement for clathrin-dependent endocytosis to activate JAK/STAT signalling suggests a model in which the signalling 'on' state relies not only on ligand binding to the receptor at the cell surface, but also on the recruitment of the complex into endocytic vesicles on their way to lysozomes. Selective activation of the pool of receptors marked for degradation thus provides a way to tightly control JAK/STAT activity.

摘要

无穹顶(Dome)是一种与白细胞介素-6相关的细胞因子受体,在果蝇发育过程中激活保守的JAK/STAT信号通路。尽管在几种模型中对信号转导通路有深入了解,但受体胞吞作用在JAK/STAT激活中的作用仍知之甚少。通过体内遗传分析和细胞培养试验,我们发现未配对1(Upd1)的配体结合诱导受体-配体复合物的网格蛋白依赖性胞吞作用,以及它们随后通过内体区室向溶酶体的运输。令人惊讶的是,使用影响网格蛋白重链、rab5、Hrs或深橙色的突变体阻断不同内体区室中的运输会导致JAK/STAT通路受到抑制,而当rab11受到影响时该通路则保持不变。这表明内化和运输对于JAK/STAT活性都是必需的。网格蛋白依赖性胞吞作用激活JAK/STAT信号的需求提示了一种模型,即信号“开启”状态不仅依赖于配体在细胞表面与受体的结合,还依赖于复合物在其前往溶酶体的途中被募集到内吞小泡中。因此,对标记用于降解的受体池的选择性激活提供了一种严格控制JAK/STAT活性的方法。

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