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通过对占据释放位点数量的活动依赖性调节来控制突触前平行纤维效能

Control of Presynaptic Parallel Fiber Efficacy by Activity-Dependent Regulation of the Number of Occupied Release Sites.

作者信息

Schmidt Hartmut

机构信息

Carl-Ludwig Institute for Physiology, Medical Faculty, University of Leipzig, Leipzig, Germany.

出版信息

Front Syst Neurosci. 2019 Jul 17;13:30. doi: 10.3389/fnsys.2019.00030. eCollection 2019.

DOI:10.3389/fnsys.2019.00030
PMID:31379524
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6650762/
Abstract

Parallel fiber (PF) synapses show pronounced and lasting facilitation during bursts of high-frequency activity. They typically connect to their target neurons a single active zone (AZ), harboring few release sites (2-8) with moderate initial vesicular release probability (0.2-0.4). In light of these biophysical characteristics, it seems surprising that PF synapses can sustain facilitation during high-frequency periods of tens of action potentials (APs). Recent findings suggest an increase in the number of occupied release sites due to ultra-rapid (~180 s), Ca dependent recruitment of synaptic vesicles (SVs) from replenishment sites as major presynaptic mechanism of this lasting facilitation. On the molecular level, Synaptotagmin 7 or Munc13s have been suggested to be involved in mediating facilitation at PF synapses. The recruitment of SVs from replenishment sites appears to be reversible on a slower time-scale, thereby, explaining that PF synapses rapidly depress and ultimately become silent during low-frequency activity. Hence, PF synapses show high-frequency facilitation (HFF) but low-frequency depression (LFD). This behavior is explained by regulation of the number of occupied release sites at the AZ by AP frequency.

摘要

平行纤维(PF)突触在高频活动爆发期间表现出明显且持久的易化作用。它们通常通过单个活性区(AZ)与靶神经元相连,该活性区含有较少的释放位点(约2 - 8个),初始囊泡释放概率适中(约0.2 - 0.4)。鉴于这些生物物理特性,PF突触在数十个动作电位(AP)的高频期能够维持易化作用,这似乎令人惊讶。最近的研究结果表明,由于超快速(约180秒)、钙依赖的突触囊泡(SV)从补充位点募集,导致被占据的释放位点数量增加,这是这种持久易化作用的主要突触前机制。在分子水平上,已表明突触结合蛋白7或Munc13s参与介导PF突触的易化作用。从补充位点募集SV似乎在较慢的时间尺度上是可逆的,从而解释了PF突触在低频活动期间迅速抑制并最终沉默的现象。因此,PF突触表现出高频易化(HFF)但低频抑制(LFD)。这种行为可以通过动作电位频率对活性区被占据的释放位点数量的调节来解释。

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本文引用的文献

1
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Front Mol Neurosci. 2019 Jan 15;11:494. doi: 10.3389/fnmol.2018.00494. eCollection 2018.
2
Dynamically Primed Synaptic Vesicle States: Key to Understand Synaptic Short-Term Plasticity.动态引发的突触囊泡状态:理解突触短期可塑性的关键。
Neuron. 2018 Dec 19;100(6):1283-1291. doi: 10.1016/j.neuron.2018.11.024.
3
Synergistic control of neurotransmitter release by different members of the synaptotagmin family.
Ca2.2通道维持成熟谷氨酸能突触处的囊泡募集。
J Neurosci. 2023 May 31;43(22):4005-4018. doi: 10.1523/JNEUROSCI.1279-22.2023. Epub 2023 Apr 26.
4
Morphofunctional changes at the active zone during synaptic vesicle exocytosis.在突触小泡胞吐过程中活性区的形态功能变化。
EMBO Rep. 2023 May 4;24(5):e55719. doi: 10.15252/embr.202255719. Epub 2023 Mar 6.
5
Three small vesicular pools in sequence govern synaptic response dynamics during action potential trains.三个小的囊泡池依次控制动作电位序列期间的突触反应动力学。
Proc Natl Acad Sci U S A. 2022 Feb 1;119(5). doi: 10.1073/pnas.2114469119.
6
Developmental Increase of Neocortical Presynaptic Efficacy Maturation of Vesicle Replenishment.新皮质突触前效能的发育性增加:囊泡补充的成熟
Front Synaptic Neurosci. 2020 Jan 15;11:36. doi: 10.3389/fnsyn.2019.00036. eCollection 2019.
不同突触结合蛋白家族成员对神经递质释放的协同控制。
Curr Opin Neurobiol. 2018 Aug;51:154-162. doi: 10.1016/j.conb.2018.05.006. Epub 2018 Jun 7.
4
Synaptotagmin 7 Mediates Both Facilitation and Asynchronous Release at Granule Cell Synapses.突触融合蛋白 7 介导颗粒细胞突触的易化和非同步释放。
J Neurosci. 2018 Mar 28;38(13):3240-3251. doi: 10.1523/JNEUROSCI.3207-17.2018.
5
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Cell Rep. 2018 Feb 20;22(8):1965-1973. doi: 10.1016/j.celrep.2018.02.010.
6
Frequency-dependent mobilization of heterogeneous pools of synaptic vesicles shapes presynaptic plasticity.频率依赖性的突触囊泡异质库的动员塑造了突触前可塑性。
Elife. 2017 Oct 9;6:e28935. doi: 10.7554/eLife.28935.
7
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8
The Mechanisms and Functions of Synaptic Facilitation.突触易化的机制与功能
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9
The readily releasable pool of synaptic vesicles.突触小泡的易释放池。
Curr Opin Neurobiol. 2017 Apr;43:63-70. doi: 10.1016/j.conb.2016.12.012. Epub 2017 Jan 16.
10
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Neuron. 2016 Aug 17;91(4):808-823. doi: 10.1016/j.neuron.2016.07.033.