Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
Dev Neurobiol. 2012 Apr;72(4):600-14. doi: 10.1002/dneu.20955.
Precise navigation of axons to their targets is critical for establishing proper neuronal networks during development. Axon elongation, whereby axons extend far beyond the site of initiation to reach their target cells, is an essential step in this process, but the precise molecular pathways that regulate axon growth remain uncharacterized. Here we show that 14-3-3/14-3-3ς proteins-adaptor proteins that modulate diverse cellular processes including cytoskeletal dynamics-play a critical role in Xenopus retinal ganglion cell (RGC) axon elongation in vivo and in vitro. We have identified the expression of 14-3-3/14-3-3ς transcripts and proteins in retinal growth cones, with higher levels of expression occurring during the phase of rapid pathway extension. Competitive inhibition of 14-3-3/14-3-3ς by expression of a genetically encoded peptide, R18, in RGCs resulted in a marked decrease in the length of the initial retinotectal projection in vivo and a corresponding decrease in axon elongation rate in vitro (30-40%). Furthermore, 14-3-3/14-3-3ς (R1) co-localized with Xenopus actin depolymerizing factor (ADF)/cofilin (XAC) in RGC growth cones. Inhibition of 14-3-3/14-3-3ς function with either R18 or morpholinos reduced the level of inactive pXAC and increased the sensitivity to collapse by the repulsive cue, Slit2. Collectively, these results demonstrate that14-3-3/14-3-3ς participates in the regulation of retinal axon elongation, in part by modulating XAC activity.
轴突精确导航到其靶标对于在发育过程中建立适当的神经元网络至关重要。轴突延伸,即轴突远远超出起始部位延伸到其靶细胞,是这个过程中的一个重要步骤,但调节轴突生长的精确分子途径仍未被描述。在这里,我们表明 14-3-3/14-3-3ς 蛋白 - 调节包括细胞骨架动力学在内的多种细胞过程的衔接蛋白 - 在活体和体外的非洲爪蟾视网膜神经节细胞 (RGC) 轴突延伸中起着关键作用。我们已经确定了 14-3-3/14-3-3ς 转录本和蛋白质在视网膜生长锥中的表达,在快速路径延伸阶段表达水平更高。在 RGC 中表达遗传编码肽 R18 对 14-3-3/14-3-3ς 的竞争抑制导致体内初始视网膜 - 视顶盖投射的长度明显减少,体外轴突延伸率相应降低 (30-40%)。此外,14-3-3/14-3-3ς (R1) 与非洲爪蟾肌动蛋白解聚因子 (ADF)/丝切蛋白 (XAC) 在 RGC 生长锥中共定位。用 R18 或 morpholino 抑制 14-3-3/14-3-3ς 功能会降低无活性 pXAC 的水平,并增加对排斥信号 Slit2 的崩溃敏感性。总之,这些结果表明 14-3-3/14-3-3ς 参与调节视网膜轴突延伸,部分通过调节 XAC 活性。