Engert F, Bonhoeffer T
Max-Planck Institute of Neurobiology, München-Martinsried, Germany.
Nature. 1999 May 6;399(6731):66-70. doi: 10.1038/19978.
Long-term enhancement of synaptic efficacy in the hippocampus is an important model for studying the cellular mechanisms of neuronal plasticity, circuit reorganization, and even learning and memory. Although these long-lasting functional changes are easy to induce, it has been very difficult to demonstrate that they are accompanied or even caused by morphological changes on the subcellular level. Here we combined a local superfusion technique with two-photon imaging, which allowed us to scrutinize specific regions of the postsynaptic dendrite where we knew that the synaptic changes had to occur. We show that after induction of long-lasting (but not short-lasting) functional enhancement of synapses in area CA1, new spines appear on the postsynaptic dendrite, whereas in control regions on the same dendrite or in slices where long-term potentiation was blocked, no significant spine growth occurred.
海马体中突触效能的长期增强是研究神经元可塑性、神经回路重组乃至学习与记忆的细胞机制的重要模型。尽管这些持久的功能变化易于诱导,但要证明它们伴随着亚细胞水平的形态变化,甚至是由这些形态变化所引起,却一直非常困难。在这里,我们将局部灌流技术与双光子成像相结合,这使我们能够仔细观察突触变化必定会发生的突触后树突的特定区域。我们发现,在诱导CA1区突触的持久(而非短暂)功能增强后,突触后树突上会出现新的棘突,而在同一树突的对照区域或长期增强被阻断的切片中,则没有明显的棘突生长。