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长时程增强(LTP)过程中N型钙离子通道的募集增强了海马CA1穿通通路突触的低释放效能。

Recruitment of N-Type Ca(2+) channels during LTP enhances low release efficacy of hippocampal CA1 perforant path synapses.

作者信息

Ahmed Mohsin S, Siegelbaum Steven A

机构信息

Department of Neuroscience, Columbia University, New York, NY 10032, USA.

出版信息

Neuron. 2009 Aug 13;63(3):372-85. doi: 10.1016/j.neuron.2009.07.013.

Abstract

The entorhinal cortex provides both direct and indirect inputs to hippocampal CA1 neurons through the perforant path and Schaffer collateral synapses, respectively. Using both two-photon imaging of synaptic vesicle cycling and electrophysiological recordings, we found that the efficacy of transmitter release at perforant path synapses is lower than at Schaffer collateral inputs. This difference is due to the greater contribution to release by presynaptic N-type voltage-gated Ca(2+) channels at the Schaffer collateral than perforant path synapses. Induction of long-term potentiation that depends on activation of NMDA receptors and L-type voltage-gated Ca(2+) channels enhances the low efficacy of release at perforant path synapses by increasing the contribution of N-type channels to exocytosis. This represents a previously uncharacterized presynaptic mechanism for fine-tuning release properties of distinct classes of synapses onto a common postsynaptic neuron and for regulating synaptic function during long-term synaptic plasticity.

摘要

内嗅皮层分别通过穿通通路和谢弗侧支突触为海马CA1神经元提供直接和间接输入。利用双光子成像技术观察突触囊泡循环以及电生理记录,我们发现穿通通路突触处递质释放的效能低于谢弗侧支输入处。这种差异是由于谢弗侧支突触前N型电压门控Ca(2+)通道对释放的贡献大于穿通通路突触。依赖于NMDA受体和L型电压门控Ca(2+)通道激活的长时程增强的诱导,通过增加N型通道对胞吐作用的贡献,增强了穿通通路突触处较低的释放效能。这代表了一种以前未被描述的突触前机制,用于微调不同类型突触在共同的突触后神经元上的释放特性,并在长期突触可塑性过程中调节突触功能。

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