兴奋性突触后钙瞬态在感觉-运动神经元突触允许在培养中对突触强度进行数天的定量检查。

IF 2.2
Learning & memory (Cold Spring Harbor, N.Y.) Pub Date : 2021-08-16 Print Date: 2021-09-01 DOI:10.1101/lm.052639.120
Tyler W Dunn, Wayne S Sossin
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引用次数: 2

摘要

对突触可塑性背后的突触强度变化的更彻底的描述可以通过对单个突触位点的量子分辨率测量来实现。在这里,我们证明,通过使用膜靶向遗传钙传感器,我们可以测量单个突触位点上的量子突触事件,感觉神经元到运动神经元的突触连接。这些结果表明,在这些培养中,突触强度不是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,大多数突触接触并没有发现相反的突触前静脉曲张,而是在突触前和突触后接触的区域没有发现明显的膜增厚。使用这种技术,可以在数天内测量单个突触接触的释放概率、量子大小和量子内容。同型突触抑制伴随着释放位点概率的降低,没有证据表明个体突触位点在抑郁过程中沉默。这项技术有望解决该系统中悬而未决的问题,包括确定维持突触强度长期变化的突触变化,这是记忆的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Excitatory postsynaptic calcium transients at <i>Aplysia</i> sensory-motor neuron synapses allow for quantal examination of synaptic strength over multiple days in culture.

Excitatory postsynaptic calcium transients at <i>Aplysia</i> sensory-motor neuron synapses allow for quantal examination of synaptic strength over multiple days in culture.

Excitatory postsynaptic calcium transients at <i>Aplysia</i> sensory-motor neuron synapses allow for quantal examination of synaptic strength over multiple days in culture.

Excitatory postsynaptic calcium transients at Aplysia sensory-motor neuron synapses allow for quantal examination of synaptic strength over multiple days in culture.

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 Aplysia 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.

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