Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4350548 | Neuroscience Letters | 2006 | 5 Pages |
Abstract
For the analysis of the cellular mechanism underlying long-term synaptic plasticity, a model system that allows long-lasting pursuit is required. Previously we reported that, in hippocampal neurons under dissociated cell culture conditions, repeated (but not a single) transient activation of protein kinase A (PKA) led to an increase in the number of synapses that lasted >3 weeks, and hence we proposed that this phenomenon should serve as an appropriate model system. Here we report that repeated pulsatile application of brain-derived neurotrophic factor (BDNF) leads to persistent synapse formation equivalent to that after the repeated transient activation of PKA. A BDNF-scavenging substance applied concomitantly with PKA activation abolished the synapse formation. The release of BDNF upon PKA activation was confirmed by phosphorylation of TrkB. These results indicate that the release of BDNF is involved in the putative signaling cascade connecting PKA activation and synapse formation.
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Authors
Naoko Taniguchi, Yo Shinoda, Nobuyuki Takei, Hiroyuki Nawa, Akihiko Ogura, Keiko Tominaga-Yoshino,