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调节活性区突触小泡释放概率的分子机器

Molecular Machines Regulating the Release Probability of Synaptic Vesicles at the Active Zone.

作者信息

Körber Christoph, Kuner Thomas

机构信息

Department of Functional Neuroanatomy, Institute of Anatomy and Cell Biology, Heidelberg University Heidelberg, Germany.

出版信息

Front Synaptic Neurosci. 2016 Mar 2;8:5. doi: 10.3389/fnsyn.2016.00005. eCollection 2016.

DOI:10.3389/fnsyn.2016.00005
PMID:26973506
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4773589/
Abstract

The fusion of synaptic vesicles (SVs) with the plasma membrane of the active zone (AZ) upon arrival of an action potential (AP) at the presynaptic compartment is a tightly regulated probabilistic process crucial for information transfer. The probability of a SV to release its transmitter content in response to an AP, termed release probability (Pr), is highly diverse both at the level of entire synapses and individual SVs at a given synapse. Differences in Pr exist between different types of synapses, between synapses of the same type, synapses originating from the same axon and even between different SV subpopulations within the same presynaptic terminal. The Pr of SVs at the AZ is set by a complex interplay of different presynaptic properties including the availability of release-ready SVs, the location of the SVs relative to the voltage-gated calcium channels (VGCCs) at the AZ, the magnitude of calcium influx upon arrival of the AP, the buffering of calcium ions as well as the identity and sensitivity of the calcium sensor. These properties are not only interconnected, but can also be regulated dynamically to match the requirements of activity patterns mediated by the synapse. Here, we review recent advances in identifying molecules and molecular machines taking part in the determination of vesicular Pr at the AZ.

摘要

当动作电位(AP)到达突触前区室时,突触小泡(SVs)与活性区(AZ)的质膜融合是一个严格调控的概率性过程,对信息传递至关重要。一个SV响应AP释放其递质内容物的概率,称为释放概率(Pr),在整个突触水平以及给定突触处的单个SV水平上都高度不同。Pr在不同类型的突触之间、同一类型的突触之间、来自同一轴突的突触之间甚至同一突触前终末内不同的SV亚群之间都存在差异。AZ处SV的Pr由不同突触前特性的复杂相互作用决定,这些特性包括随时可释放的SV的可用性、SV相对于AZ处电压门控钙通道(VGCCs)的位置、AP到达时钙内流的大小、钙离子的缓冲以及钙传感器的特性和敏感性。这些特性不仅相互关联,还可以动态调节以匹配由突触介导的活动模式的需求。在这里,我们综述了在识别参与确定AZ处囊泡Pr的分子和分子机器方面的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8235/4773589/a8bc06d51ec2/fnsyn-08-00005-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8235/4773589/e3a14f4bbf99/fnsyn-08-00005-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8235/4773589/62cf2f5bbf6d/fnsyn-08-00005-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8235/4773589/a8bc06d51ec2/fnsyn-08-00005-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8235/4773589/e3a14f4bbf99/fnsyn-08-00005-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8235/4773589/62cf2f5bbf6d/fnsyn-08-00005-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8235/4773589/a8bc06d51ec2/fnsyn-08-00005-g0003.jpg

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1
The calcium sensor synaptotagmin 7 is required for synaptic facilitation.突触易化需要钙传感器突触结合蛋白7。
Nature. 2016 Jan 7;529(7584):88-91. doi: 10.1038/nature16507.
2
Presynaptic Deletion of GIT Proteins Results in Increased Synaptic Strength at a Mammalian Central Synapse.突触前GIT蛋白缺失导致哺乳动物中枢突触的突触强度增加。
Neuron. 2015 Dec 2;88(5):918-925. doi: 10.1016/j.neuron.2015.10.042.
3
The trans-SNARE-regulating function of Munc18-1 is essential to synaptic exocytosis.Munc18-1的跨SNARE调节功能对于突触胞吐作用至关重要。
bioRxiv. 2025 Mar 29:2025.02.13.637710. doi: 10.1101/2025.02.13.637710.
4
Minimal presynaptic protein machinery governing diverse kinetics of calcium-evoked neurotransmitter release.调控钙诱发神经递质释放多种动力学的最小突触前蛋白机制。
Nat Commun. 2024 Dec 30;15(1):10741. doi: 10.1038/s41467-024-54960-1.
5
Spinal microcircuits go through multiphasic homeostatic compensations in a mouse model of motoneuron degeneration.在运动神经元变性的小鼠模型中,脊髓微回路经历多相稳态补偿。
Cell Rep. 2024 Dec 24;43(12):115046. doi: 10.1016/j.celrep.2024.115046. Epub 2024 Dec 9.
6
A minimal presynaptic protein machinery mediating synchronous and asynchronous exocytosis and short-term plasticity.一种介导同步和异步胞吐作用以及短期可塑性的最小突触前蛋白机制。
bioRxiv. 2024 Apr 18:2024.04.15.589559. doi: 10.1101/2024.04.15.589559.
7
Spinal microcircuits go through multiphasic homeostatic compensations in a mouse model of motoneuron degeneration.在运动神经元变性的小鼠模型中,脊髓微回路经历多相稳态补偿。
bioRxiv. 2024 Oct 12:2024.04.10.588918. doi: 10.1101/2024.04.10.588918.
8
Synaptopathies in Developmental and Epileptic Encephalopathies: A Focus on Pre-synaptic Dysfunction.发育性和癫痫性脑病中的突触病变:聚焦于突触前功能障碍
Front Neurol. 2022 Mar 8;13:826211. doi: 10.3389/fneur.2022.826211. eCollection 2022.
9
Determinants of synapse diversity revealed by super-resolution quantal transmission and active zone imaging.超高分辨率量子传递和活性区成像揭示的突触多样性决定因素。
Nat Commun. 2022 Jan 11;13(1):229. doi: 10.1038/s41467-021-27815-2.
10
The decoy SNARE Tomosyn sets tonic versus phasic release properties and is required for homeostatic synaptic plasticity.诱饵 SNAP25 样蛋白 Tomosyn 设定了强直释放与瞬态释放特性,并对维持性突触可塑性具有必要性。
Elife. 2021 Oct 29;10:e72841. doi: 10.7554/eLife.72841.
Nat Commun. 2015 Nov 17;6:8852. doi: 10.1038/ncomms9852.
4
Imaging Exocytosis of Single Synaptic Vesicles at a Fast CNS Presynaptic Terminal.在快速中枢神经系统突触前末端对单个突触囊泡的胞吐作用进行成像。
Neuron. 2015 Nov 4;88(3):492-8. doi: 10.1016/j.neuron.2015.09.047.
5
Vesicular Synaptobrevin/VAMP2 Levels Guarded by AP180 Control Efficient Neurotransmission.囊泡相关膜蛋白 2(Vesicular Synaptobrevin/VAMP2)水平受 AP180 调控,可维持高效的神经传递。
Neuron. 2015 Oct 21;88(2):330-44. doi: 10.1016/j.neuron.2015.08.034. Epub 2015 Sep 24.
6
RIM-BPs Mediate Tight Coupling of Action Potentials to Ca(2+)-Triggered Neurotransmitter Release.RIM-BPs 介导动作电位与 Ca(2+)-触发神经递质释放的紧密偶联。
Neuron. 2015 Sep 23;87(6):1234-1247. doi: 10.1016/j.neuron.2015.08.027.
7
Merits and Limitations of Vesicle Pool Models in View of Heterogeneous Populations of Synaptic Vesicles.囊泡池模型在考虑突触囊泡异质性群体方面的优缺点。
Neuron. 2015 Sep 23;87(6):1131-1142. doi: 10.1016/j.neuron.2015.08.038.
8
Ca(2+) current facilitation determines short-term facilitation at inhibitory synapses between cerebellar Purkinje cells.钙离子电流易化作用决定小脑浦肯野细胞间抑制性突触的短期易化。
J Physiol. 2015 Nov 15;593(22):4889-904. doi: 10.1113/JP270704. Epub 2015 Oct 12.
9
An Engineered Metal Sensor Tunes the Kinetics of Synaptic Transmission.一种工程金属传感器可调节突触传递的动力学。
J Neurosci. 2015 Aug 26;35(34):11769-79. doi: 10.1523/JNEUROSCI.1694-15.2015.
10
Architecture of the synaptotagmin-SNARE machinery for neuronal exocytosis.用于神经元胞吐作用的突触结合蛋白-SNARE机制的结构
Nature. 2015 Sep 3;525(7567):62-7. doi: 10.1038/nature14975. Epub 2015 Aug 17.