Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, Quebec H3A 2B4, Canada.
Learn Mem. 2021 Aug 16;28(9):277-290. doi: 10.1101/lm.052639.120. Print 2021 Sep.
A more thorough description of the changes in synaptic strength underlying synaptic plasticity may be achieved with quantal resolution measurements at individual synaptic sites. Here, we demonstrate that by using a membrane targeted genetic calcium sensor, we can measure quantal synaptic events at the individual synaptic sites of sensory neuron to motor neuron synaptic connections. These results show that synaptic strength is not evenly distributed between all contacts in these cultures, but dominated by multiquantal sites of synaptic contact, likely clusters of individual synaptic sites. Surprisingly, most synaptic contacts were not found opposite presynaptic varicosities, but instead at areas of pre- and postsynaptic contact with no visible thickening of membranes. The release probability, quantal size, and quantal content can be measured over days at individual synaptic contacts using this technique. Homosynaptic depression was accompanied by a reduction in release site probability, with no evidence of individual synaptic site silencing over the course of depression. This technique shows promise in being able to address outstanding questions in this system, including determining the synaptic changes that maintain long-term alterations in synaptic strength that underlie memory.
通过在单个突触位点进行量子分辨率测量,可能可以更深入地描述突触可塑性中突触强度的变化。在这里,我们证明通过使用膜靶向遗传钙传感器,我们可以测量感觉神经元到运动神经元突触连接的单个突触位点的量子突触事件。这些结果表明,在这些培养物中,突触强度并非均匀分布在所有接触点之间,而是由突触接触的多量子位点主导,可能是单个突触位点的集群。令人惊讶的是,大多数突触接触点不是在突触前膨体对面发现的,而是在突触前和突触后接触的区域,没有可见的膜增厚。使用这种技术,可以在单个突触接触点上连续几天测量释放概率、量子大小和量子含量。同突触抑制伴随着释放位点概率的降低,在抑制过程中没有证据表明单个突触位点沉默。这项技术有望能够解决该系统中的一些悬而未决的问题,包括确定维持记忆背后突触强度长期改变的突触变化。