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本文引用的文献

1
What is Rate-Limiting during Sustained Synaptic Activity: Vesicle Supply or the Availability of Release Sites.在持续的突触活动中,限制速率的因素是什么:是囊泡供应还是释放位点的可用性。
Front Synaptic Neurosci. 2010 Sep 16;2:144. doi: 10.3389/fnsyn.2010.00144. eCollection 2010.
2
Synaptic vesicle pools: an update.突触囊泡池:更新。
Front Synaptic Neurosci. 2010 Oct 5;2:135. doi: 10.3389/fnsyn.2010.00135. eCollection 2010.
3
The role of presynaptic dynamics in processing of natural spike trains in hippocampal synapses.在海马突触中,突触前动力学在自然尖峰序列处理中的作用。
J Neurosci. 2010 Nov 24;30(47):15904-14. doi: 10.1523/JNEUROSCI.4050-10.2010.
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Control of neurotransmitter release: From Ca2+ to voltage dependent G-protein coupled receptors.控制神经递质释放:从 Ca2+到电压依赖性 G 蛋白偶联受体。
Pflugers Arch. 2010 Nov;460(6):975-90. doi: 10.1007/s00424-010-0872-7. Epub 2010 Sep 2.
5
Perisynaptic glia discriminate patterns of motor nerve activity and influence plasticity at the neuromuscular junction.突触周胶质细胞能够区分运动神经活动的模式,并影响神经肌肉接头的可塑性。
J Neurosci. 2010 Sep 1;30(35):11870-82. doi: 10.1523/JNEUROSCI.3165-10.2010.
6
Differential regulation of synchronous versus asynchronous neurotransmitter release by the C2 domains of synaptotagmin 1.通过突触融合蛋白 1 的 C2 结构域对同步与异步神经递质释放进行差异调节。
Proc Natl Acad Sci U S A. 2010 Aug 17;107(33):14869-74. doi: 10.1073/pnas.1000606107. Epub 2010 Aug 2.
7
Interaction between facilitation and depression at a large CNS synapse reveals mechanisms of short-term plasticity.在大型中枢神经系统突触中促进和抑郁的相互作用揭示了短期可塑性的机制。
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Synaptotagmin has an essential function in synaptic vesicle positioning for synchronous release in addition to its role as a calcium sensor.突触结合蛋白除了作为钙传感器发挥作用外,在突触小泡定位以实现同步释放方面也具有重要功能。
Neuron. 2009 Aug 27;63(4):482-96. doi: 10.1016/j.neuron.2009.07.028.
9
A general model of synaptic transmission and short-term plasticity.突触传递与短期可塑性的通用模型。
Neuron. 2009 May 28;62(4):539-54. doi: 10.1016/j.neuron.2009.03.025.
10
Modeling short-term synaptic plasticity at the calyx of Held using in vivo-like stimulation patterns.使用类体内刺激模式模拟海氏神经节处的短期突触可塑性。
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在模式化神经刺激期间,神经肌肉突触中促进短期突触可塑性的增强元件数量随着细胞外 Ca2+ 从低水平到正常水平改变而逐渐减少,从而使基础释放概率从低水平增加到正常水平。

The number of components of enhancement contributing to short-term synaptic plasticity at the neuromuscular synapse during patterned nerve Stimulation progressively decreases as basal release probability is increased from low to normal levels by changing extracellular Ca2+.

机构信息

Department of Physiology and Biophysics and Neuroscience Program, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.

出版信息

J Neurosci. 2011 May 11;31(19):7060-72. doi: 10.1523/JNEUROSCI.0392-11.2011.

DOI:10.1523/JNEUROSCI.0392-11.2011
PMID:21562268
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6703210/
Abstract

Presynaptic short-term plasticity (STP) dynamically modulates synaptic strength in a reversible manner on a timescale of milliseconds to minutes. For low basal vesicular release probability (prob0), four components of enhancement, F1 and F2 facilitation, augmentation (A), and potentiation (P), increase synaptic strength during repetitive nerve activity. For release rates that exceed the rate of replenishment of the readily releasable pool (RRP) of synaptic vesicles, depression of synaptic strength, observed as a rundown of postsynaptic potential amplitudes, can also develop. To understand the relationship between enhancement and depression at the frog (Rana pipiens) neuromuscular synapse, data obtained over a wide range of prob0 using patterned stimulation are analyzed with a hybrid model to reveal the components of STP. We find that F1, F2, A, P, and depletion of the RRP all contribute to STP during repetitive nerve activity at low prob0. As prob0 is increased by raising Ca(o)(2+) (extracellular Ca2+), specific components of enhancement no longer contribute, with first P, then A, and then F2 becoming undetectable, even though F1 continues to enhance release. For levels of prob0 that lead to appreciable depression, only F1 and depletion of the RRP contribute to STP during rundown, and for low stimulation rates, F2 can also contribute. These observations place prob0-dependent limitations on which components of enhancement contribute to STP and suggest some fundamental mechanistic differences among the components. The presented model can serve as a tool to readily characterize the components of STP over wide ranges of prob0.

摘要

突触前短期可塑性(STP)以毫秒到分钟的时间尺度动态调节突触强度,这种调节是可逆的。在基础囊泡释放概率(prob0)较低的情况下,增强的四个成分(F1 和 F2 易化、增强(A)和增强(P))在重复神经活动期间增加突触强度。对于释放速率超过突触囊泡易释放池(RRP)补充速率的情况,突触强度也会出现抑制,表现为突触后电位幅度的衰减。为了了解在青蛙(Rana pipiens)神经肌肉突触中增强和抑制之间的关系,我们使用模式化刺激在广泛的 prob0 范围内获得数据,并使用混合模型进行分析,以揭示 STP 的成分。我们发现,在低 prob0 时,F1、F2、A、P 和 RRP 的耗竭都会导致重复神经活动期间的 STP。随着 Ca(o)(2+)(细胞外 Ca2+)的增加,增强的特定成分不再起作用,首先是 P,然后是 A,然后是 F2 变得无法检测,尽管 F1 仍在增强释放。对于导致明显抑制的 prob0 水平,只有 F1 和 RRP 的耗竭会在衰减期间导致 STP,并且对于低刺激率,F2 也可以贡献。这些观察结果表明,prob0 依赖性限制了增强的哪些成分有助于 STP,并表明这些成分之间存在一些基本的机制差异。所提出的模型可以作为一种工具,在广泛的 prob0 范围内快速表征 STP 的成分。