Department of Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.
Cold Spring Harb Perspect Biol. 2013 May 1;5(5):a017459. doi: 10.1101/cshperspect.a017459.
Endocytosis is the major regulator of signaling from receptor tyrosine kinases (RTKs). The canonical model of RTK endocytosis involves rapid internalization of an RTK activated by ligand binding at the cell surface and subsequent sorting of internalized ligand-RTK complexes to lysosomes for degradation. Activation of the intrinsic tyrosine kinase activity of RTKs results in autophosphorylation, which is mechanistically coupled to the recruitment of adaptor proteins and conjugation of ubiquitin to RTKs. Ubiquitination serves to mediate interactions of RTKs with sorting machineries both at the cell surface and on endosomes. The pathways and kinetics of RTK endocytic trafficking, molecular mechanisms underlying sorting processes, and examples of deviations from the standard trafficking itinerary in the RTK family are discussed in this work.
内吞作用是受体酪氨酸激酶(RTKs)信号转导的主要调节剂。RTK 内吞作用的典型模型包括:配体与细胞表面结合激活 RTK 后,RTK 快速内化,随后将内化的配体-RTK 复合物分拣到溶酶体进行降解。RTKs 的内在酪氨酸激酶活性的激活导致自身磷酸化,这与衔接蛋白的募集和泛素与 RTKs 的缀合在机制上偶联。泛素化有助于介导 RTKs 与细胞表面和内体上的分选机制的相互作用。本文讨论了 RTK 内吞运输的途径和动力学、分选过程的分子机制,以及 RTK 家族中偏离标准运输轨迹的实例。