Department of Biochemistry, Oxford University, Oxford OX1 3QU, United Kingdom; email:
Wellcome Trust Centre for Human Genetics, Oxford University, Oxford OX3 7BN, United Kingdom; email:
Annu Rev Cell Dev Biol. 2016 Oct 6;32:577-608. doi: 10.1146/annurev-cellbio-111315-125008. Epub 2016 Aug 24.
Axon guidance relies on a combinatorial code of receptor and ligand interactions that direct adhesive/attractive and repulsive cellular responses. Recent structural data have revealed many of the molecular mechanisms that govern these interactions and enabled the design of sophisticated mutant tools to dissect their biological functions. Here, we discuss the structure/function relationships of four major classes of guidance cues (ephrins, semaphorins, slits, netrins) and examples of morphogens (Wnt, Shh) and of cell adhesion molecules (FLRT). These cell signaling systems rely on specific modes of receptor-ligand binding that are determined by selective binding sites; however, defined structure-encoded receptor promiscuity also enables cross talk between different receptor/ligand families and can also involve extracellular matrix components. A picture emerges in which a multitude of highly context-dependent structural assemblies determines the finely tuned cellular behavior required for nervous system development.
轴突导向依赖于受体和配体相互作用的组合密码,这些相互作用指导细胞的黏附/吸引和排斥反应。最近的结构数据揭示了许多控制这些相互作用的分子机制,并使设计复杂的突变工具来剖析它们的生物学功能成为可能。在这里,我们讨论了四大类导向线索(ephrins、semaphorins、slits、netrins)和形态发生素(Wnt、Shh)以及细胞黏附分子(FLRT)的结构/功能关系。这些细胞信号系统依赖于特定的受体-配体结合模式,这些模式由选择性结合位点决定;然而,定义明确的结构编码受体的混杂性也允许不同的受体/配体家族之间的串扰,并且还可以涉及细胞外基质成分。一幅画面出现了,即大量高度依赖上下文的结构组装决定了神经系统发育所需的精细调节的细胞行为。