Taniguchi Naoko, Shinoda Yo, Takei Nobuyuki, Nawa Hiroyuki, Ogura Akihiko, Tominaga-Yoshino Keiko
Department of Neuroscience, Osaka University Graduate School of Frontier Biosciences, Machikaneyama-cho 1-1, Toyonaka, Osaka 560-0043, Japan.
Neurosci Lett. 2006 Oct 2;406(1-2):38-42. doi: 10.1016/j.neulet.2006.06.071. Epub 2006 Aug 9.
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.
为了分析长期突触可塑性背后的细胞机制,需要一个能够实现长期追踪的模型系统。此前我们报道,在解离细胞培养条件下的海马神经元中,蛋白激酶A(PKA)的重复(而非单次)瞬时激活会导致突触数量增加,且这种增加可持续超过3周,因此我们提出这一现象应作为一个合适的模型系统。在此我们报道,重复脉冲式应用脑源性神经营养因子(BDNF)会导致持续的突触形成,这与PKA重复瞬时激活后的情况相当。与PKA激活同时应用的BDNF清除物质可消除突触形成。通过TrkB的磷酸化证实了PKA激活时BDNF的释放。这些结果表明,BDNF的释放参与了连接PKA激活与突触形成的假定信号级联反应。