Dunn Tyler W, Syed Naweed I
Hotchkiss Brain Institute, Department of Cell Biology and Anatomy, Faculty of Medicine, University of Calgary, 3330 Hospital Drive, NW, Calgary, Alberta T2N4N1, Canada.
Eur J Neurosci. 2006 Sep;24(6):1591-605. doi: 10.1111/j.1460-9568.2006.05028.x.
The mechanisms by which presynaptic neurones differentially regulate synaptic transmission with multiple postsynaptic targets in the brain are not fully understood. Using intracellular sharp electrode and whole-cell voltage-clamp recordings of soma-soma synapses between identified Lymnaea neurones, we provide direct evidence that quantal size is regulated presynaptically through the coupling of multiple release sites. This coupling effectively multiplies quantal size, thereby providing significant influence over parameters of synaptic transmission that are influenced by quantal size, such as the variance in transmitter release at stationary release probabilities. Variation in the degree of coupling is dependent on the identity of the postsynaptic cell, even though the variation in quantal size is of presynaptic origin. We have therefore demonstrated the presence of a novel mechanism by which presynaptic neurones may differentially regulate quantal size at select synaptic connections, in turn providing them with a means of regulating synaptic transmission with multiple postsynaptic cells.
在大脑中,突触前神经元如何对多个突触后靶点进行突触传递的差异调节,其机制尚未完全明确。利用细胞内尖锐电极和全细胞电压钳记录法,对已鉴定的椎实螺神经元之间的体细胞-体细胞突触进行研究,我们提供了直接证据,证明量子大小是通过多个释放位点的耦合在突触前受到调节的。这种耦合有效地使量子大小成倍增加,从而对受量子大小影响的突触传递参数产生重大影响,例如在固定释放概率下递质释放的方差。耦合程度的变化取决于突触后细胞的类型,尽管量子大小的变化源于突触前。因此,我们证明了一种新机制的存在,通过该机制突触前神经元可以在特定突触连接中差异调节量子大小,进而为它们提供一种调节与多个突触后细胞的突触传递的方式。