Vahdat Zahra, Gambrell Oliver, Fisch Jonas, Friauf Eckhard, Singh Abhyudai
Department of Electrical and Computer Engineering, University of Delaware, Newark, Delaware, United States of America.
Animal Physiology Group, Department of Biology, University of Kaiserslautern, Kaiserslautern, Germany.
PLoS Comput Biol. 2025 May 13;21(5):e1013067. doi: 10.1371/journal.pcbi.1013067. eCollection 2025 May.
Quantal parameters of synapses are fundamental for the temporal dynamics of neurotransmitter release, which is the basis of interneuronal communication. We formulate a general class of models that capture the stochastic dynamics of quantal content (QC), defined as the number of SV fusion events triggered by a single action potential (AP). Considering the probabilistic and time-varying nature of SV docking, undocking, and AP-triggered fusion, we derive an exact statistical distribution for the QC over time. Analyzing this distribution at steady-state and its associated autocorrelation function, we show that QC fluctuation statistics can be leveraged for inferring key presynaptic parameters, such as the probability of SV fusion (release probability) and SV replenishment at empty docking sites (refilling probability). Our model predictions are tested with electrophysiological data obtained from 50-Hz stimulation of auditory MNTB-LSO synapses in brainstem slices from juvenile mice. Our results show that while synaptic depression can be explained by low and constant refilling/release probabilities, this scenario is inconsistent with the statistics of the electrophysiological data, which show a low QC Fano factor and almost uncorrelated successive QCs. Our systematic analysis yields a model that couples a high release probability to a time-varying refilling probability to explain both the synaptic depression and its associated statistical fluctuations. In summary, we provide a general approach that exploits stochastic signatures in QCs to infer neurotransmission regulating processes that cannot be distinguished from simple analysis of averaged synaptic responses.
突触的量子参数对于神经递质释放的时间动态至关重要,而神经递质释放是神经元间通讯的基础。我们构建了一类通用模型,该模型捕捉量子含量(QC)的随机动态,量子含量定义为单个动作电位(AP)触发的突触小泡(SV)融合事件的数量。考虑到SV对接、解对接以及AP触发融合的概率性和时变性质,我们推导出了QC随时间变化的精确统计分布。通过分析稳态下的这种分布及其相关的自相关函数,我们表明可以利用QC波动统计来推断关键的突触前参数,例如SV融合的概率(释放概率)以及空对接位点处SV的补充(再填充概率)。我们用从幼年小鼠脑干切片中对听觉内侧核团到外侧上橄榄核(MNTB-LSO)突触进行50赫兹刺激所获得的电生理数据来检验我们的模型预测。我们的结果表明,虽然突触抑制可以用低且恒定的再填充/释放概率来解释,但这种情况与电生理数据的统计结果不一致,电生理数据显示出低的QC法诺因子以及几乎不相关的连续QC。我们的系统分析得出了一个模型,该模型将高释放概率与随时间变化的再填充概率相结合,以解释突触抑制及其相关的统计波动。总之,我们提供了一种通用方法,该方法利用QC中的随机特征来推断神经传递调节过程,而这些过程无法通过对平均突触反应的简单分析来区分。