Porter B E, Weis J, Sanes J R
Department of Anatomy and Neurobiology Washington University School of Medicine St. Louis, Missouri 63110.
Neuron. 1995 Mar;14(3):549-59. doi: 10.1016/0896-6273(95)90311-9.
Motor axons preferentially reinnervate original synaptic sites on denervated muscle fibers. We have shown that components of synaptic basal lamina direct this selectivity, and we identified a protein, s-laminin, that is concentrated in synaptic basal lamina. Here, we report that a recombinant s-laminin fragment inhibits neurite outgrowth promoted by laminin. A tripeptide sequence in this fragment, Leu-Arg-Glu (LRE), contributes to this inhibition and is itself sufficient to inhibit outgrowth. LRE-mediated inhibition is selective for motoneuron-like cells and is observed in mixtures with several, but not all, outgrowth-promoting substrates. Growth cones extending on laminin stop for up to several hours upon contacting deposits of the s-laminin fragment. Thus, LRE may serve as a cell type-selective and context-dependent target-derived signal that plays a role in synapse formation.
运动轴突优先重新支配失神经支配的肌纤维上的原始突触位点。我们已经表明,突触基底层的成分指导这种选择性,并且我们鉴定出一种蛋白质,即s-层粘连蛋白,它集中在突触基底层中。在此,我们报告一种重组s-层粘连蛋白片段抑制层粘连蛋白促进的神经突生长。该片段中的一个三肽序列,亮氨酸-精氨酸-谷氨酸(LRE),促成这种抑制作用,并且其本身就足以抑制生长。LRE介导的抑制作用对运动神经元样细胞具有选择性,并且在与几种(但不是全部)促进生长的底物混合时可以观察到。在层粘连蛋白上延伸的生长锥在接触s-层粘连蛋白片段的沉积物时会停止长达数小时。因此,LRE可能作为一种细胞类型选择性且依赖于环境的靶标衍生信号,在突触形成中发挥作用。