Alsina B, Vu T, Cohen-Cory S
Mental Retardation Research Center, Department of Psychiatry and Biobehavioral Sciences, 760 Westwood Plaza, NPI 58-258, University of California Los Angeles, Los Angeles, California 90095, USA.
Nat Neurosci. 2001 Nov;4(11):1093-101. doi: 10.1038/nn735.
Dynamic developmental changes in axon arbor morphology may directly reflect the formation, stabilization and elimination of synapses. We used dual-color imaging to study, in the live, developing animal, the relationship between axon arborization and synapse formation at the single cell level, and to examine the participation of brain-derived neurotrophic factor (BDNF) in synaptogenesis. Green fluorescent protein (GFP)-tagged synaptobrevin II served as a marker to visualize synaptic sites in individual fluorescently labeled Xenopus optic axons. Time-lapse confocal microscopy revealed that although most synapses remain stable, synapses are also formed and eliminated as axons branch and increase their complexity. Most new branches originated at GFP-labeled synaptic sites. Increasing BDNF levels significantly increased both axon arborization and synapse number, with BDNF increasing synapse number per axon terminal. The ability to visualize central synapses in real time provides insights about the dynamic mechanisms underlying synaptogenesis, and reveals BDNF as a modulator of synaptogenesis in vivo.
轴突分支形态的动态发育变化可能直接反映突触的形成、稳定和消除。我们利用双色成像技术,在活体发育动物中研究单细胞水平上轴突分支与突触形成之间的关系,并检验脑源性神经营养因子(BDNF)在突触发生中的作用参与情况。绿色荧光蛋白(GFP)标记的突触小泡蛋白II作为一种标记物,用于可视化单个荧光标记的非洲爪蟾视轴突中的突触位点。延时共聚焦显微镜显示,虽然大多数突触保持稳定,但随着轴突分支并增加其复杂性,突触也会形成和消除。大多数新分支起源于GFP标记的突触位点。增加BDNF水平显著增加了轴突分支和突触数量,BDNF增加了每个轴突末端的突触数量。实时可视化中枢突触的能力为突触发生的动态机制提供了见解,并揭示BDNF作为体内突触发生的调节剂。