Arai Itaru, Jonas Peter
IST Austria (Institute of Science and Technology Austria), Klosterneuburg, Austria.
Elife. 2014 Dec 9;3:e04057. doi: 10.7554/eLife.04057.
A puzzling property of synaptic transmission, originally established at the neuromuscular junction, is that the time course of transmitter release is independent of the extracellular Ca(2+) concentration ([Ca(2+)]o), whereas the rate of release is highly [Ca(2+)]o-dependent. Here, we examine the time course of release at inhibitory basket cell-Purkinje cell synapses and show that it is independent of [Ca(2+)]o. Modeling of Ca(2+)-dependent transmitter release suggests that the invariant time course of release critically depends on tight coupling between Ca(2+) channels and release sensors. Experiments with exogenous Ca(2+) chelators reveal that channel-sensor coupling at basket cell-Purkinje cell synapses is very tight, with a mean distance of 10-20 nm. Thus, tight channel-sensor coupling provides a mechanistic explanation for the apparent [Ca(2+)]o independence of the time course of release.
突触传递的一个令人费解的特性最初是在神经肌肉接头处发现的,即递质释放的时间进程与细胞外Ca(2+)浓度([Ca(2+)]o)无关,而释放速率则高度依赖于[Ca(2+)]o。在这里,我们研究了抑制性篮状细胞 - 浦肯野细胞突触处的释放时间进程,并表明它与[Ca(2+)]o无关。对Ca(2+)依赖性递质释放的建模表明,释放的不变时间进程关键取决于Ca(2+)通道与释放传感器之间的紧密耦合。使用外源性Ca(2+)螯合剂的实验表明,篮状细胞 - 浦肯野细胞突触处的通道 - 传感器耦合非常紧密,平均距离为10 - 20纳米。因此,紧密的通道 - 传感器耦合为释放时间进程明显的[Ca(2+)]o独立性提供了一个机制解释。