Zakharenko Stanislav S, Zablow Leonard, Siegelbaum Steven A
Center for Neurobiology and Behavior, Department of Pharmacology, Howard Hughes Medical Institute, Columbia University, New York, NY 10032, USA.
Neuron. 2002 Sep 12;35(6):1099-110. doi: 10.1016/s0896-6273(02)00898-x.
The site of modification of synaptic transmission during long-term plasticity in the mammalian hippocampus remains controversial. Here we used a fluorescent marker of presynaptic activity, FM 1-43, to directly image presynaptic function during metabotropic glutamate receptor-dependent long-term depression (mGluR-LTD) at CA3-CA1 excitatory synapses in acute hippocampal slices. We found a significant decrease in the rate of FM 1-43 release in response to synaptic stimulation following induction of mGluR-LTD, providing direct evidence for altered presynaptic function. Moreover, we found that mGluR-LTD causes several changes in FM dye release properties that are consistent with a change in the mode of vesicle cycling, possibly involving a switch from a full fusion mode of release to a "kiss-and-run" mode of release through the transient opening of a fusion pore.
在哺乳动物海马体中,长期可塑性过程中突触传递的修饰位点仍存在争议。在此,我们使用了一种突触前活动的荧光标记物FM 1-43,来直接成像急性海马切片中CA3-CA1兴奋性突触处代谢型谷氨酸受体依赖性长时程抑制(mGluR-LTD)期间的突触前功能。我们发现,诱导mGluR-LTD后,响应突触刺激的FM 1-43释放速率显著降低,这为突触前功能改变提供了直接证据。此外,我们发现mGluR-LTD会导致FM染料释放特性发生多种变化,这些变化与囊泡循环模式的改变一致,可能涉及从完全融合释放模式转变为通过融合孔的短暂开放实现的“亲吻-逃离”释放模式。