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发育中的桶状皮层关键期前突触形成过程中,相邻柱之间第2/3层水平连接的尖峰时间依赖性可塑性。

Spike Timing-Dependent Plasticity at Layer 2/3 Horizontal Connections Between Neighboring Columns During Synapse Formation Before the Critical Period in the Developing Barrel Cortex.

作者信息

Itami Chiaki, Kimura Fumitaka

机构信息

Department of Physiology, Faculty of Medicine, Saitama Medical University, Moroyama, Saitama 350-0495, Japan.

Laboratory of Brain Neuroscience, Faculty of Health Care Sciences, Jikei University of Health Care Sciences, Osaka 532-0003, Japan.

出版信息

Cells. 2025 Sep 18;14(18):1459. doi: 10.3390/cells14181459.

DOI:10.3390/cells14181459
PMID:41002424
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12468516/
Abstract

The Hebbian type of spike timing-dependent plasticity (STDP) with long-term potentiation and depression (LTP and LTD) plays a crucial role at layer 4 (L4) to L2/3 synapses in deprivation-induced map plasticity. In addition, plasticity at the L2/3 horizontal connection is suggested to play an additional role in map plasticity, especially for "spared whisker response potentiation." Unimodal STDP with only LTP, or all-LTP STDP drives circuit formation at thalamocortical, as well as L4-L2/3 synapse before the critical period. Here, we first show that the L2/3 horizontal connections exhibit all-LTP STDP when axons are extending during synapse formation before the critical period. LTP-STDP induced by pre-post timing was mediated by NMDA-R because APV blocked the induction. In addition, PKA signaling was involved because PKI 6-22 blocked the induction. However, LTP-STDP induced by post-pre timing was not mediated by NMDA-R, because APV could not block its induction. Nevertheless, PKA signaling was also involved in its induction because PKI 6-22 blocked the induction. Our finding indicates that PKA signaling plays an important role in all-LTP STDP during synaptic formation at the L2/3-L2/3 connection between neighboring columns with a distinct source of Ca influx in the developing mouse barrel cortex.

摘要

具有长时程增强和抑制(LTP和LTD)的赫布型脉冲时间依赖性可塑性(STDP)在剥夺诱导的图谱可塑性中,于第4层(L4)至第2/3层突触处发挥着关键作用。此外,第2/3层水平连接的可塑性被认为在图谱可塑性中发挥额外作用,特别是对于“保留的触须反应增强”。仅具有LTP的单峰STDP或全LTP STDP在关键期之前驱动丘脑皮质以及L4 - L2/3突触处的电路形成。在此,我们首先表明,在关键期之前突触形成过程中轴突延伸时,第2/3层水平连接表现出全LTP STDP。由前 - 后时间诱导的LTP - STDP由NMDA - R介导,因为APV阻断了诱导。此外,PKA信号传导参与其中,因为PKI 6 - 22阻断了诱导。然而,由后 - 前时间诱导的LTP - STDP不由NMDA - R介导,因为APV不能阻断其诱导。尽管如此,PKA信号传导也参与其诱导,因为PKI 6 - 22阻断了诱导。我们的发现表明,在发育中的小鼠桶状皮质中,相邻柱之间第2/3 - 第2/3连接的突触形成过程中,PKA信号传导在全LTP STDP中起重要作用,且有不同的钙内流来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdb3/12468516/bcff6eb75981/cells-14-01459-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdb3/12468516/90e6717a2293/cells-14-01459-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdb3/12468516/10d0f13a83ff/cells-14-01459-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdb3/12468516/bcff6eb75981/cells-14-01459-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdb3/12468516/90e6717a2293/cells-14-01459-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdb3/12468516/10d0f13a83ff/cells-14-01459-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdb3/12468516/bcff6eb75981/cells-14-01459-g003.jpg

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本文引用的文献

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A Hypothetical Model Concerning How Spike-Timing-Dependent Plasticity Contributes to Neural Circuit Formation and Initiation of the Critical Period in Barrel Cortex.关于尖峰时间依赖可塑性如何有助于皮层桶状结构的神经回路形成和关键期起始的假设模型。
J Neurosci. 2019 May 15;39(20):3784-3791. doi: 10.1523/JNEUROSCI.1684-18.2019. Epub 2019 Mar 15.
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Developmental Switch in Spike Timing-Dependent Plasticity and Cannabinoid-Dependent Reorganization of the Thalamocortical Projection in the Barrel Cortex.桶状皮层中丘脑皮质投射的峰时依赖可塑性和大麻素依赖重组的发育转变
J Neurosci. 2016 Jun 29;36(26):7039-54. doi: 10.1523/JNEUROSCI.4280-15.2016.
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Developmental switch in spike timing-dependent plasticity at layers 4-2/3 in the rodent barrel cortex.
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