Hansen S M, Berezin V, Bock E
ENKAM Pharmaceuticals A/S, Fruebjergvej 3, Copenhagen Ø, 2100 Denmark.
Cell Mol Life Sci. 2008 Nov;65(23):3809-21. doi: 10.1007/s00018-008-8290-0.
Formation of appropriate neural circuits depends on a complex interplay between extracellular guiding cues and intracellular signaling events that result in alterations of cytoskeletal dynamics and a neurite growth response. Surface-expressed cell adhesion molecules (CAMs) interact with the surroundings via the extracellular domain and bind to the cytoskeleton via their intracellular domain. In addition, several CAMs induce signaling events via direct interactions with intracellular proteins or via interactions with cell surface receptors. Thus, CAMs are obvious candidates for transmitting extracellular guidance cues to intracellular events and thereby regulating neurite outgrowth. In this review, we focus on two CAMs, the neural cell adhesion molecule (NCAM) and N-cadherin, and their ability to mediate signaling associated with a neurite outgrowth response. In particular, we will focus on direct interaction between NCAM and N-cadherin with a number of intracellular partners, as well as on their interaction with the fibroblast growth factor receptor (FGFR).
合适神经回路的形成取决于细胞外引导线索与细胞内信号事件之间复杂的相互作用,这些相互作用会导致细胞骨架动力学的改变和神经突生长反应。表面表达的细胞粘附分子(CAMs)通过细胞外结构域与周围环境相互作用,并通过其细胞内结构域与细胞骨架结合。此外,几种CAMs通过与细胞内蛋白质的直接相互作用或与细胞表面受体的相互作用诱导信号事件。因此,CAMs显然是将细胞外引导线索传递到细胞内事件并由此调节神经突生长的候选分子。在本综述中,我们聚焦于两种CAMs,即神经细胞粘附分子(NCAM)和N-钙粘蛋白,以及它们介导与神经突生长反应相关信号传导的能力。特别地,我们将关注NCAM和N-钙粘蛋白与许多细胞内伙伴之间的直接相互作用,以及它们与成纤维细胞生长因子受体(FGFR)的相互作用。