Malartre Marianne
Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Université Paris-Sud, Université Paris-Saclay, 91198, Gif-sur-Yvette Cedex, France.
Cell Mol Life Sci. 2016 May;73(9):1825-43. doi: 10.1007/s00018-016-2153-x. Epub 2016 Mar 2.
EGFR signalling is a well-conserved signalling pathway playing major roles during development and cancers. This review explores what studying the EGFR pathway during Drosophila eye development has taught us in terms of the diversity of its regulatory mechanisms. This model system has allowed the identification of numerous positive and negative regulators acting at specific time and place, thus participating to the tight control of signalling. EGFR signalling regulation is achieved by a variety of mechanisms, including the control of ligand processing, the availability of the receptor itself and the transduction of the cascade in the cytoplasm. Ultimately, the transcriptional responses contribute to the establishment of positive and negative feedback loops. The combination of these multiple mechanisms employed to regulate the EGFR pathway leads to specific cellular outcomes involved in functions as diverse as the acquisition of cell fate, proliferation, survival, adherens junction remodelling and morphogenesis.
表皮生长因子受体(EGFR)信号通路是一条在发育和癌症过程中发挥重要作用的高度保守的信号通路。本综述探讨了在果蝇眼睛发育过程中对EGFR通路的研究在其调控机制多样性方面给我们带来的启示。这个模型系统使我们能够鉴定出在特定时间和位置起作用的众多正负调节因子,从而参与信号的严格控制。EGFR信号通路的调控是通过多种机制实现的,包括配体加工的控制、受体本身的可用性以及细胞质中信号级联的转导。最终,转录反应有助于建立正负反馈回路。用于调节EGFR通路的这些多种机制的组合导致了涉及多种功能的特定细胞结果,如细胞命运的获得、增殖、存活、黏着连接重塑和形态发生。