突触可塑性和内在神经放电在小鼠视觉皮层第四层微电路发育中的功能作用。

IF 1.5 4区 医学 Q3 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Sanwu Liu, Yinyun Li
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引用次数: 0

摘要

小鼠初级视觉皮层发育关键期的开始和出生后第14天睁眼之间是一个复杂的过程,对视觉认知功能至关重要。小鼠初级视觉皮层关键期的开始涉及到各神经元的内在放电特性和突触的短期可塑性的改变。为了研究各因子在可塑性关键期调控回路放电活动中的功能作用,我们采用Markram的短期可塑性模型和Wilson的内在神经元放电活动模型,基于实验结果的连接概率构建了小鼠视觉皮层第四层微电路。结果表明,在CP发育过程中,调控微电路放电模式的最关键因素是PC到PV和SST中间神经元突触的短期可塑性,其上调PV中间神经元的放电,在兴奋和抑制之间形成新的平衡;PC和PV在发育过程中的固有放电活动降低了电路的放电频率。此外,我们还研究了CP过程中丘脑皮层前馈兴奋性投射到PC和PV中间神经元的功能,发现神经放电活动在很大程度上依赖于TC输入,结果与局部回路相似,差异较小。我们认为,临界期的短期塑性发育对电路行为的调节起着至关重要的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Deciphering functional roles of synaptic plasticity and intrinsic neural firing in developing mouse visual cortex layer IV microcircuit.

Deciphering functional roles of synaptic plasticity and intrinsic neural firing in developing mouse visual cortex layer IV microcircuit.

Between the onset of the critical period of mouse primary visual cortex and eye opening at postnatal day 14 is a complex process and that is vital for the cognitive function of vision. The onset of the critical period of mouse primary visual cortex involves changes of the intrinsic firing property of each neuron and short term plasticity of synapses. In order to investigate the functional role of each factor in regulating the circuit firing activity during the critical period plasticity, we adopted the Markram's model for short term plasticity and Wilson's model for intrinsic neuron firing activity, and construct a microcircuit for mouse visual cortex layer IV based on the connection probabilities from experimental results. Our results indicate that, during CP development, the most critical factors that regulate the firing pattern of microcircuit is the short term plasticity of the synapse from PC to PV and SST interneurons, which upregulates the PV interneuron firing and produces new balance between excitation and inhibition; the intrinsic firing activity of PC and PV during development downregulates the firing frequency of the circuits. In addition, we have investigated the function of feedforward excitatory thalamic-cortical projection to PC and PV interneuron during CP, and found that neural firing activity largely depends on the TC input and the results are similar to the local circuit with minor differences. We conclude that the short term plasticity development during critical period plays a crucial role in regulating the circuit behavior.

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来源期刊
CiteScore
2.00
自引率
8.30%
发文量
32
审稿时长
3 months
期刊介绍: The Journal of Computational Neuroscience provides a forum for papers that fit the interface between computational and experimental work in the neurosciences. The Journal of Computational Neuroscience publishes full length original papers, rapid communications and review articles describing theoretical and experimental work relevant to computations in the brain and nervous system. Papers that combine theoretical and experimental work are especially encouraged. Primarily theoretical papers should deal with issues of obvious relevance to biological nervous systems. Experimental papers should have implications for the computational function of the nervous system, and may report results using any of a variety of approaches including anatomy, electrophysiology, biophysics, imaging, and molecular biology. Papers investigating the physiological mechanisms underlying pathologies of the nervous system, or papers that report novel technologies of interest to researchers in computational neuroscience, including advances in neural data analysis methods yielding insights into the function of the nervous system, are also welcomed (in this case, methodological papers should include an application of the new method, exemplifying the insights that it yields).It is anticipated that all levels of analysis from cognitive to cellular will be represented in the Journal of Computational Neuroscience.
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