Department of Chemical Biology, Leiden University Medical Center LUMC, Einthovenweg 22, 2333 ZC, Leiden, The Netherlands.
Department of Chemical Biology, Leiden University Medical Center LUMC, Einthovenweg 22, 2333 ZC, Leiden, The Netherlands
J Cell Sci. 2017 Dec 15;130(24):4087-4096. doi: 10.1242/jcs.209197. Epub 2017 Nov 27.
When cell surface receptors engage their cognate ligands in the extracellular space, they become competent to transmit potent signals to the inside of the cell, thereby instigating growth, differentiation, motility and many other processes. In order to control these signals, activated receptors are endocytosed and thoroughly curated by the endosomal network of intracellular vesicles and proteolytic organelles. In this Review, we follow the epidermal growth factor (EGF) receptor (EGFR) from ligand engagement, through its voyage on endosomes and, ultimately, to its destruction in the lysosome. We focus on the spatial and temporal considerations underlying the molecular decisions that govern this complex journey and discuss how additional cellular organelles - particularly the ER - play active roles in the regulation of receptor lifespan. In summarizing the functions of relevant molecules on the endosomes and the ER, we cover the order of molecular events in receptor activation, trafficking and downregulation, and provide an overview of how signaling is controlled at the interface between these organelles.
当细胞表面受体在细胞外空间与它们的配体结合时,它们就能够向细胞内部传递有效的信号,从而启动细胞的生长、分化、迁移和许多其他过程。为了控制这些信号,激活的受体被内吞,并被细胞内囊泡和蛋白水解细胞器的内体网络进行彻底的修饰。在这篇综述中,我们以表皮生长因子(EGF)受体(EGFR)为例,从配体结合开始,追踪它在内体上的旅程,最终在溶酶体中被破坏。我们专注于控制这一复杂过程的分子决策的时空考虑因素,并讨论了其他细胞细胞器——特别是内质网(ER)——如何在受体寿命的调节中发挥积极作用。通过总结内体和 ER 上相关分子的功能,我们涵盖了受体激活、运输和下调过程中的分子事件顺序,并概述了信号如何在这些细胞器之间的界面上得到控制。