Pasquale Elena B
Cancer Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
Trends Biochem Sci. 2024 Dec;49(12):1079-1096. doi: 10.1016/j.tibs.2024.10.002. Epub 2024 Nov 12.
Eph receptor tyrosine kinases, together with their cell surface-anchored ephrin ligands, constitute an important cell-cell communication system that regulates physiological and pathological processes in most cell types. This review focuses on the multiple mechanisms by which Eph receptors initiate signaling via the formation of protein complexes in the plasma membrane. Upon ephrin binding, Eph receptors assemble into oligomers that can further aggregate into large complexes. Eph receptors also mediate ephrin-independent signaling through interplay with intracellular kinases or other cell-surface receptors. The distinct characteristics of Eph receptor family members, as well as their conserved domain structure, provide a framework for understanding their functional differences and redundancies. Possible areas of interest for future investigations of Eph receptor signaling complexes are also highlighted.
Eph受体酪氨酸激酶与其细胞表面锚定的ephrin配体共同构成了一个重要的细胞间通讯系统,该系统调节大多数细胞类型中的生理和病理过程。本综述重点关注Eph受体通过在质膜中形成蛋白质复合物来启动信号传导的多种机制。在ephrin结合后,Eph受体组装成寡聚体,这些寡聚体可进一步聚集形成大的复合物。Eph受体还通过与细胞内激酶或其他细胞表面受体的相互作用介导不依赖ephrin的信号传导。Eph受体家族成员的独特特征及其保守的结构域结构为理解它们的功能差异和冗余提供了一个框架。本文还强调了未来对Eph受体信号复合物进行研究可能感兴趣的领域。