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新皮质突触前效能的发育性增加:囊泡补充的成熟

Developmental Increase of Neocortical Presynaptic Efficacy Maturation of Vesicle Replenishment.

作者信息

Bornschein Grit, Brachtendorf Simone, Schmidt Hartmut

机构信息

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

出版信息

Front Synaptic Neurosci. 2020 Jan 15;11:36. doi: 10.3389/fnsyn.2019.00036. eCollection 2019.

DOI:10.3389/fnsyn.2019.00036
PMID:32009937
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6974464/
Abstract

The efficacy of neocortical synapses to transmit during bursts of action potentials (APs) increases during development but the underlying mechanisms are largely unclear. We investigated synaptic efficacy at synapses between layer 5 pyramidal neurons (L5PNs) during development, using paired recordings, presynaptic two-photon Ca imaging, and numerical simulations. Our data confirm a developmental increase in paired-pulse ratios (PPRs). Independent of age, Ca imaging revealed no AP invasion failures and linear summation of presynaptic Ca transients, making differences in Ca signaling an unlikely reason for developmental changes in PPR. Cumulative excitatory postsynaptic current (EPSC) amplitudes indicate that neither the size of the readily-releasable pool (RRP) nor replenishment rates were different between age groups, while the time-courses of depression differed significantly. At young synapses, EPSCs depressed rapidly to near steady-state during the first four APs, and synaptic failures (F) increased from 0 to 30%. At mature synapses this drop was significantly slower and strongly biphasic, such that near steady-state depression was reached not before 18 APs with F remaining between 0 and 5%. While young synapses reliably transmitted during pairs of APs, albeit with strong depression, mature synapses maintained near 100% transfer efficacy with significantly less depression during high-frequency bursts of APs. Our analysis indicates that at mature synapses a replenishment pool (RepP) is responsible for their high efficacy during bursting activity, while this RepP is functionally immature at young synapses. Hence, our data provide evidence that the functional maturation of a RepP underlies increasing synaptic efficacy during the development of an excitatory cortical synapse.

摘要

新皮质突触在动作电位(AP)爆发期间传递的效能在发育过程中会增加,但其潜在机制在很大程度上尚不清楚。我们使用配对记录、突触前双光子钙成像和数值模拟,研究了发育过程中第5层锥体神经元(L5PNs)之间突触的效能。我们的数据证实了配对脉冲比率(PPR)在发育过程中的增加。与年龄无关,钙成像显示没有AP侵入失败以及突触前钙瞬变的线性总和,这使得钙信号差异不太可能是PPR发育变化的原因。累积兴奋性突触后电流(EPSC)幅度表明,不同年龄组之间即时可释放池(RRP)的大小和补充率均无差异,而抑制的时间进程则有显著差异。在年轻突触中,EPSC在前四个AP期间迅速抑制至接近稳态,突触失败(F)从0增加到30%。在成熟突触中,这种下降明显较慢且呈强烈的双相性,即直到18个AP之后才达到接近稳态的抑制,F保持在0至5%之间。虽然年轻突触在成对AP期间能够可靠地传递,尽管有强烈的抑制,但成熟突触在AP高频爆发期间保持接近100%的传递效能,且抑制明显较少。我们的分析表明,在成熟突触中,一个补充池(RepP)负责其在爆发活动期间的高效能,而这个RepP在年轻突触中功能不成熟。因此,我们的数据提供了证据,表明RepP的功能成熟是兴奋性皮质突触发育过程中突触效能增加的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d711/6974464/79e5c85ca5ed/fnsyn-11-00036-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d711/6974464/94d1e64396d4/fnsyn-11-00036-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d711/6974464/0d175b6ebfb3/fnsyn-11-00036-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d711/6974464/dc031d18202f/fnsyn-11-00036-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d711/6974464/79e5c85ca5ed/fnsyn-11-00036-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d711/6974464/94d1e64396d4/fnsyn-11-00036-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d711/6974464/0d175b6ebfb3/fnsyn-11-00036-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d711/6974464/dc031d18202f/fnsyn-11-00036-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d711/6974464/79e5c85ca5ed/fnsyn-11-00036-g0004.jpg

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Cell Rep. 2019 Aug 6;28(6):1410-1418.e4. doi: 10.1016/j.celrep.2019.07.008.
2
Control of Presynaptic Parallel Fiber Efficacy by Activity-Dependent Regulation of the Number of Occupied Release Sites.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
Front Syst Neurosci. 2019 Jul 17;13:30. doi: 10.3389/fnsys.2019.00030. eCollection 2019.
3
Dynamically Primed Synaptic Vesicle States: Key to Understand Synaptic Short-Term Plasticity.
Brain. 2025 Feb 21. doi: 10.1093/brain/awaf074.
4
Dysfunction of proprioceptive sensory synapses is a pathogenic event and therapeutic target in mice and humans with spinal muscular atrophy.本体感觉感觉突触功能障碍是脊髓性肌萎缩症小鼠和人类的致病事件及治疗靶点。
medRxiv. 2024 Jun 4:2024.06.03.24308132. doi: 10.1101/2024.06.03.24308132.
5
Interpretation of presynaptic phenotypes of synaptic plasticity in terms of a two-step priming process.根据两步引发过程来解释突触可塑性的突触前表型。
J Gen Physiol. 2024 Jan 1;156(1). doi: 10.1085/jgp.202313454. Epub 2023 Dec 19.
6
Fully-primed slowly-recovering vesicles mediate presynaptic LTP at neocortical neurons.完全预极化的慢速恢复小泡介导新皮层神经元的突触前 LTP。
Proc Natl Acad Sci U S A. 2023 Oct 24;120(43):e2305460120. doi: 10.1073/pnas.2305460120. Epub 2023 Oct 19.
7
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8
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9
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5
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6
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7
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8
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9
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10
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