Tebar Francesc, Gelabert-Baldrich Mariona, Hoque Monira, Cairns Rose, Rentero Carles, Pol Albert, Grewal Thomas, Enrich Carlos
Departament de Biologia Cellular, Immunologia i Neurociències, IDIBAPS, Facultat de Medicina, Universitat de Barcelona, Barcelona, Spain.
Faculty of Pharmacy, University of Sydney, Sydney, New South Wales, Australia.
Methods Enzymol. 2014;535:55-74. doi: 10.1016/B978-0-12-397925-4.00004-3.
Cell signaling and endocytosis are intimately linked in eukaryotic cells. Signaling receptors at the cell surface enter the endocytic pathway and continue to activate downstream effectors in endosomal compartments. This spatiotemporal regulation of signal transduction provides opportunity for signal diversity and a cell-specific machinery of scaffolding/targeting proteins contributes to establish compartment-specific signaling complexes. Members of the annexin (Anx) protein family, in particular AnxA1, AnxA2, and AnxA6, appear to target their interaction partners to specific membrane microdomains to contribute to the formation of compartment-specific signaling platforms along the endocytic pathway. A major challenge to understand the impact of scaffolding/targeting proteins on spatiotemporal signal transduction along endocytic pathways is the identification, isolation, and functional analysis of low-abundance signal-transducing protein complexes in endocytic compartments. Here, we describe methods to isolate endosomes and to target signaling molecules to endosomes. Applying these methodologies to suitable animal or cell models will enable the dissection of signal transduction in the endocytic compartment in the presence or absence of annexins.
在真核细胞中,细胞信号传导与内吞作用紧密相连。细胞表面的信号受体进入内吞途径,并继续在内体区室中激活下游效应器。这种信号转导的时空调节为信号多样性提供了机会,并且一种细胞特异性的支架/靶向蛋白机制有助于建立区室特异性信号复合物。膜联蛋白(Anx)蛋白家族的成员,特别是AnxA1、AnxA2和AnxA6,似乎将其相互作用伙伴靶向特定的膜微区,以促进沿内吞途径形成区室特异性信号平台。理解支架/靶向蛋白对沿内吞途径的时空信号转导的影响的一个主要挑战是在内体区室中鉴定、分离和功能分析低丰度信号转导蛋白复合物。在这里,我们描述了分离内体并将信号分子靶向内体的方法。将这些方法应用于合适的动物或细胞模型将能够在有或没有膜联蛋白的情况下剖析内体区室中的信号转导。