Saikia Queen, Reeve Hannah, Alzahrani Areej, Critchley William R, Zeqiraj Elton, Divan Aysha, Harrison Michael A, Ponnambalam Sreenivasan
School of Molecular & Cellular Biology, University of Leeds, Leeds, United Kingdom.
School of Biomedical Sciences, University of Leeds, Leeds, United Kingdom.
Prog Mol Biol Transl Sci. 2023;194:109-139. doi: 10.1016/bs.pmbts.2022.06.021. Epub 2022 Jul 15.
The binding of vascular endothelial growth factor (VEGF) superfamily to VEGF receptor tyrosine kinases (VEGFRs) and co-receptors regulates vasculogenesis, angiogenesis and lymphangiogenesis. A recurring theme is that dysfunction in VEGF signaling promotes pathological angiogenesis, an important feature of cancer and pro-inflammatory disease states. Endocytosis of basal (resting) or activated VEGFRs facilitates signal attenuation and endothelial quiescence. However, increasing evidence suggest that activated VEGFRs can continue to signal from intracellular compartments such as endosomes. In this chapter, we focus on the evolving link between VEGFR endocytosis, signaling and turnover and the implications for angiogenesis. There is much interest in how such understanding of VEGFR dynamics can be harnessed therapeutically for a wide range of human disease states.
血管内皮生长因子(VEGF)超家族与VEGF受体酪氨酸激酶(VEGFRs)及共受体的结合调节血管生成、血管新生和淋巴管生成。一个反复出现的主题是,VEGF信号传导功能障碍会促进病理性血管新生,这是癌症和促炎性疾病状态的一个重要特征。基础(静息)或活化的VEGFRs的内吞作用有助于信号衰减和内皮细胞静止。然而,越来越多的证据表明,活化的VEGFRs可以在内体等细胞内区室继续发出信号。在本章中,我们重点关注VEGFR内吞作用、信号传导和周转之间不断演变的联系以及对血管新生的影响。人们对如何利用这种对VEGFR动态变化的理解来治疗多种人类疾病状态非常感兴趣。