Gustafsson Bengt, Ma Rong, Hanse Eric
Department of Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Front Synaptic Neurosci. 2019 Mar 7;11:7. doi: 10.3389/fnsyn.2019.00007. eCollection 2019.
Advanced imaging techniques have revealed that synapses contain nanomodules in which pre- and post-synaptic molecules are brought together to form an integrated subsynaptic component for vesicle release and transmitter reception. Based on data from an electrophysiological study of ours in which release from synapses containing a single nanomodule was induced by brief 50 Hz trains using minimal stimulation, and on data from such imaging studies, we present a possible modus operandi of such a nanomodule. We will describe the techniques and tools used to obtain and analyze the electrophysiological data from single CA3-CA1 hippocampal synapses from the neonatal rat brain. This analysis leads to the proposal that a nanomodule, despite containing a number of release locations, operates as a single release site, releasing at most a single vesicle at a time. In this nanomodule there appears to be two separate sets of release locations, one set that is responsible for release in response to the first few action potentials and another set that produces the release thereafter. The data also suggest that vesicles at the first set of release locations are primed by synaptic inactivity lasting seconds, this synaptic inactivity also resulting in a large heterogeneity in the values for vesicle release probability among the synapses. The number of vesicles being primed at this set of release locations prior to the arrival of an action potential is small (0-3) and varies from train to train. Following the first action potential, this heterogeneity in vesicle release probability largely vanishes in a release-independent manner, shaping a variation in paired-pulse plasticity among the synapses. After the first few action potentials release is produced from the second set of release locations, and is given by vesicles that have been recruited after the onset of synaptic activity. This release depends on the number of such release locations and the recruitment to such a location. The initial heterogeneity in vesicle release probability, its disappearance after a single action potential, and variation in the recruitment to the second set of release locations are instrumental in producing the heterogeneity in short-term synaptic plasticity among these synapses, and can be seen as means to create differential dynamics within a synapse population.
先进的成像技术显示,突触包含纳米模块,在该模块中,突触前和突触后分子聚集在一起,形成一个整合的亚突触组件,用于囊泡释放和递质接收。基于我们的一项电生理研究数据(该研究中,使用最小刺激,通过短暂的50赫兹串刺激诱导含有单个纳米模块的突触释放)以及此类成像研究数据,我们提出了这种纳米模块可能的运作方式。我们将描述用于获取和分析新生大鼠脑海马CA3-CA1单突触电生理数据的技术和工具。该分析得出的结论是,尽管纳米模块包含多个释放位点,但它作为一个单一的释放位点运作,一次最多释放一个囊泡。在这个纳米模块中,似乎有两组独立的释放位点,一组负责对最初的几个动作电位做出反应而释放,另一组则在随后产生释放。数据还表明,第一组释放位点的囊泡通过持续数秒的突触无活动状态进行预处理,这种突触无活动状态还导致突触间囊泡释放概率值存在很大的异质性。在动作电位到达之前,在这组释放位点被预处理的囊泡数量很少(0 - 3个),并且每次串刺激之间会有所不同。在第一个动作电位之后,囊泡释放概率的这种异质性在很大程度上以与释放无关的方式消失,形成了突触间配对脉冲可塑性的变化。在最初的几个动作电位之后,释放从第二组释放位点产生,由突触活动开始后募集的囊泡进行释放。这种释放取决于此类释放位点的数量以及向该位点的募集情况。囊泡释放概率最初的异质性、在单个动作电位后其消失以及向第二组释放位点募集的变化,有助于产生这些突触间短期突触可塑性的异质性,并且可以被视为在突触群体中创造差异动态的手段。