Visualizing synapse formation in arborizing optic axons in vivo: dynamics and modulation by BDNF.

Nat Neurosci

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.

Published: November 2001

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.

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http://dx.doi.org/10.1038/nn735DOI Listing

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