Center for Theoretical Biological Physics, University of California at San Diego, La Jolla, California, USA.
PLoS Comput Biol. 2010 Nov 11;6(11):e1000983. doi: 10.1371/journal.pcbi.1000983.
We study local calcium dynamics leading to a vesicle fusion in a stochastic, and spatially explicit, biophysical model of the CA3-CA1 presynaptic bouton. The kinetic model for vesicle release has two calcium sensors, a sensor for fast synchronous release that lasts a few tens of milliseconds and a separate sensor for slow asynchronous release that lasts a few hundred milliseconds. A wide range of data can be accounted for consistently only when a refractory period lasting a few milliseconds between releases is included. The inclusion of a second sensor for asynchronous release with a slow unbinding site, and thereby a long memory, affects short-term plasticity by facilitating release. Our simulations also reveal a third time scale of vesicle release that is correlated with the stimulus and is distinct from the fast and the slow releases. In these detailed Monte Carlo simulations all three time scales of vesicle release are insensitive to the spatial details of the synaptic ultrastructure. Furthermore, our simulations allow us to identify features of synaptic transmission that are universal and those that are modulated by structure.
我们研究了 CA3-CA1 突触前末梢的随机、空间显式生物物理模型中导致囊泡融合的局部钙动力学。囊泡释放的动力学模型有两个钙传感器,一个用于持续数十毫秒的快速同步释放的传感器,和一个用于持续数百毫秒的独立的用于慢速异步释放的传感器。只有当包括释放之间持续几毫秒的不应期时,才能始终如一地解释广泛的数据。包含用于具有缓慢离解位点的异步释放的第二个传感器,从而具有长记忆,通过促进释放来影响短期可塑性。我们的模拟还揭示了与刺激相关的第三个囊泡释放时间尺度,与快速和慢速释放不同。在这些详细的蒙特卡罗模拟中,所有三个囊泡释放的时间尺度都不受突触超微结构的空间细节的影响。此外,我们的模拟使我们能够识别突触传递的普遍特征和受结构调制的特征。