Caldieri Giusi, Malabarba Maria Grazia, Di Fiore Pier Paolo, Sigismund Sara
Dipartimento di Oncologia ed Emato-oncologia, Università degli Studi di Milano, Via Santa Sofia 9/1, 20122, Milan, Italy.
Istituto Europeo di Oncologia, Via Ripamonti 435, 20141, Milan, Italy.
Prog Mol Subcell Biol. 2018;57:235-272. doi: 10.1007/978-3-319-96704-2_9.
Signaling from the epidermal growth factor receptor (EGFR) elicits multiple biological responses, including cell proliferation, migration, and survival. Receptor endocytosis and trafficking are critical physiological processes that control the strength, duration, diversification, and spatial restriction of EGFR signaling through multiple mechanisms, which we review in this chapter. These mechanisms include: (i) regulation of receptor density and activation at the cell surface; (ii) concentration of receptors into distinct nascent endocytic structures; (iii) commitment of the receptor to different endocytic routes; (iv) endosomal sorting and postendocytic trafficking of the receptor through distinct pathways, and (v) recycling to restricted regions of the cell surface. We also highlight how communication between organelles controls EGFR activity along the endocytic route. Finally, we illustrate how abnormal trafficking of EGFR oncogenic mutants, as well as alterations of the endocytic machinery, contributes to aberrant EGFR signaling in cancer.
表皮生长因子受体(EGFR)发出的信号引发多种生物学反应,包括细胞增殖、迁移和存活。受体的内吞作用和运输是关键的生理过程,通过多种机制控制EGFR信号的强度、持续时间、多样性和空间限制,我们将在本章对此进行综述。这些机制包括:(i)细胞表面受体密度和激活的调节;(ii)受体集中到不同的新生内吞结构中;(iii)受体进入不同内吞途径的定向;(iv)受体通过不同途径进行内体分选和内吞后运输,以及(v)循环到细胞表面的特定区域。我们还强调了细胞器之间的通讯如何在内吞途径中控制EGFR活性。最后,我们举例说明了EGFR致癌突变体的异常运输以及内吞机制的改变如何导致癌症中EGFR信号异常。