Laboratory of Cell & Developmental Signaling, National Cancer Institute-Frederick, Frederick, MD 21702, USA.
Semin Cell Dev Biol. 2012 Feb;23(1):65-74. doi: 10.1016/j.semcdb.2011.10.012. Epub 2011 Oct 21.
Great strides have been made regarding our understanding of the processes and signaling events influenced by Eph/ephrin signaling that play a role in cell adhesion and cell movement. However, the precise mechanisms by which these signaling events regulate cell and tissue architecture still need further resolution. The Eph/ephrin signaling pathways and the ability to regulate cell-cell adhesion and motility constitutes an impressive system for regulating tissue separation and morphogenesis (Pasquale, 2005, 2008 [1,2]). Moreover, the de-regulation of this signaling system is linked to the promotion of aggressive and metastatic tumors in humans [2]. In the following section, we discuss some of the interesting mechanisms by which ephrins can signal through their own intracellular domains (reverse signaling) either independent of forward signaling or in addition to forward signaling through a cognate receptor. In this review we discuss how ephrins (Eph ligands) "reverse signal" through their intracellular domains to affect cell adhesion and movement, but the focus is on modes of action that are independent of SH2 and PDZ interactions.
在理解 Eph/ephrin 信号对细胞黏附和细胞运动有影响的过程和信号事件方面,已经取得了重大进展。然而,这些信号事件调节细胞和组织架构的确切机制仍需要进一步解决。Eph/ephrin 信号通路以及调节细胞-细胞黏附和运动的能力构成了一个调节组织分离和形态发生的令人印象深刻的系统(Pasquale,2005,2008 [1,2])。此外,该信号系统的失调与促进人类侵袭性和转移性肿瘤有关[2]。在接下来的部分中,我们讨论了一些 Ephrins 通过其自身细胞内结构域(反向信号)进行信号传递的有趣机制,这些机制既可以独立于正向信号,也可以与通过同源受体的正向信号相结合。在这篇综述中,我们讨论了 Ephrins(Eph 配体)如何通过其细胞内结构域“反向信号”来影响细胞黏附和运动,但重点是独立于 SH2 和 PDZ 相互作用的作用模式。