Leprince Corinne, Le Scolan Erwan, Meunier Brigitte, Fraisier Vincent, Brandon Nathalie, De Gunzburg Jean, Camonis Jacques
INSERM U528, Institut Curie Section de Recherche, 26 rue d'Ulm, 75248 Paris Cedex 05, France.
J Cell Sci. 2003 May 15;116(Pt 10):1937-48. doi: 10.1242/jcs.00403. Epub 2003 Mar 26.
Endocytosis is a regulated physiological process by which membrane receptors and their extracellular ligands are internalized. After internalization, they enter the endosomal trafficking pathway for sorting and processing. Amphiphysins consist of a family of proteins conserved throughout evolution that are crucial elements of the endocytosis machinery in mammalian cells. They act as adaptors for a series of proteins important for the endocytic process, such as dynamin. In order to improve our knowledge of amphiphysin function, we performed a two-hybrid screen with the N-terminal part of murine amphiphysin 2 (residues 1-304). One of the interacting clones corresponded to sorting nexin 4 (SNX4), a member of the SNX family of proteins which are suspected to regulate vesicular trafficking. This interaction was confirmed in vivo by co-immunoprecipitation. Immunofluorescence analysis revealed that amphiphysin 2 might bind reticulo-vesicular structures present throughout the cell body and be associated with SNX4 on these structures. In an endocytosis assay, overexpressed C-terminal or full-length SNX4 was able to inhibit transferrin receptor endocytosis as efficiently as the SH3 domain of amphiphysin 2. At lower levels of expression, SNX4 colocalized with transferrin-containing vesicles, some of which were also positive for amphiphysin 2. These results indicate that SNX4 may be part of the endocytic machinery or, alternatively, that SNX4 may associate with key elements of endocytosis such as amphiphysin 2 and sequester them when overexpressed. The presence of amphiphysin 2 on intracellular vesicles and its interplay with SNX4, which is likely to take part in intracellular trafficking, suggest that amphiphysin 2 is not only a regulator of the early steps of endocytosis. It could also play a role at the surface of the endocytic vesicle that has just been formed and of the future endosomes, in order to regulate intracellular trafficking.
内吞作用是一种受调控的生理过程,通过该过程膜受体及其细胞外配体被内化。内化后,它们进入内体运输途径进行分选和加工。发动蛋白由一类在进化过程中保守的蛋白质组成,是哺乳动物细胞内吞作用机制的关键元件。它们作为一系列对内吞过程重要的蛋白质(如发动蛋白)的衔接蛋白。为了增进我们对发动蛋白功能的了解,我们用小鼠发动蛋白2的N端部分(第1至304位氨基酸残基)进行了双杂交筛选。其中一个相互作用的克隆对应分选连接蛋白4(SNX4),它是SNX蛋白家族的成员之一,该家族蛋白被怀疑参与调控囊泡运输。这种相互作用通过共免疫沉淀在体内得到证实。免疫荧光分析显示,发动蛋白2可能与遍布细胞体的网状囊泡结构结合,并在这些结构上与SNX4相关联。在内吞作用测定中,过表达的C端或全长SNX4能够像发动蛋白2的SH3结构域一样有效地抑制转铁蛋白受体内吞作用。在较低表达水平时,SNX4与含转铁蛋白的囊泡共定位,其中一些囊泡对发动蛋白2也呈阳性。这些结果表明,SNX4可能是内吞作用机制的一部分,或者,SNX4可能与内吞作用的关键元件(如发动蛋白2)相关联,并在过表达时隔离它们。发动蛋白2在细胞内囊泡上的存在及其与可能参与细胞内运输的SNX4的相互作用表明,发动蛋白2不仅是内吞作用早期步骤的调节因子。它还可能在刚形成的内吞囊泡表面以及未来的内体表面发挥作用,以调控细胞内运输。