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Fig. 4. Anti-BDNF rapidly influences presynaptic site and axon branch stability. (A) Diagrammatic representation of GFP-synaptobrevin cluster dynamics and arbor growth. The number of GFP-synaptobrevin clusters stabilized and eliminated, and the number of new GFP-synaptobrevin clusters added between observation intervals was calculated and normalized for each time interval to obtain a dynamic measure of synapse addition and stabilization over time. As new GFP-synaptobrevin clusters are added, the absolute number of clusters that are stabilized increases, but as a proportion it remains relatively constant. The hypothetical axon depicted here exhibits rates of synapse stabilization that are slightly higher than those observed for RGC axon arbors in vehicle-treated tadpoles (control). (B) Detailed analysis of the number and distribution of GFP-synaptobrevin clusters per axon branch, and of the lifetimes of individual GFP-synaptobrevin clusters for every observation period reveal the effects of neutralizing endogenous BDNF on synapse stabilization. Anti-BDNF significantly reduced the stability of GFP-synaptobrevin clusters by 2 hours (0-2 hours), an effect that was maintained through every observation period. (C) Analysis of the number of axon branches that are retained or eliminated from one observation interval to the next provides a measure of the effects of anti-BDNF on axon branch stability. Axon branches are significantly destabilized and eliminated 0-2 hours after treatment and this effect is maintained for the first 6 hours following treatment. On average, 60.2±2.6% of branches are stable every 2 hours in anti-BDNF treated arbors versus 73.3±1.6% in controls. *P≤0.05; **P≤0.005.





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