Morales M, Colicos M A, Goda Y
Division of Biology, University of California, San Diego, La Jolla 92093, USA.
Neuron. 2000 Sep;27(3):539-50. doi: 10.1016/s0896-6273(00)00064-7.
Depolymerization of actin by latrunculin A transiently promotes neurotransmitter release. The mean rate of mEPSCs increases by a Ca2+-independent process, without a concomitant change in the mean amplitude. The readily releasable vesicle pool size and the rate of refilling of the readily releasable pool remain unaltered by latrunculin treatment. Evoked neurotransmitter release also increases in a manner consistent with an increase in vesicle release probability. The observed enhancement of neurotransmitter release is specific to actin depolymerization mediated by latrunculin A and is not caused by cytochalasin D. Our findings indicate that actin participates in a regulatory mechanism that restrains fusion of synaptic vesicles at the active zone.
Latrunculin A介导的肌动蛋白解聚可短暂促进神经递质释放。微小兴奋性突触后电流(mEPSCs)的平均频率通过一个不依赖Ca2+的过程增加,而平均幅度没有相应变化。Latrunculin处理后,易释放囊泡池的大小和易释放池的再填充速率保持不变。诱发的神经递质释放也以与囊泡释放概率增加相一致的方式增加。观察到的神经递质释放增强是由Latrunculin A介导的肌动蛋白解聚所特有的,而非细胞松弛素D所致。我们的研究结果表明,肌动蛋白参与了一种调节机制,该机制可抑制突触小泡在活性区的融合。