首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Modeling a layer 4-to-layer 2/3 module of a single column in rat neocortex: Interweaving in vitro and in vivo experimental observations
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Modeling a layer 4-to-layer 2/3 module of a single column in rat neocortex: Interweaving in vitro and in vivo experimental observations

机译:在大鼠新皮层中对单列的第4层至第2/3层模块进行建模:体内和体外实验观察的交织

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We report a step in constructing an in silico model of a neocortical column, focusing on the synaptic connection between layer 4 (L4) spiny neurons and L2/3 pyramidal cells in rat barrel cortex. It is based first on a detailed morphological and functional characterization of synaptically connected pairs of L4-L2/3 neurons from in vitro recordings and second, on in vivo recordings of voltage responses of L2/3 pyramidal cells to current pulses and to whisker deflection. In vitro data and a detailed compartmental model of L2/3 pyramidal cells enabled us to extract their specific membrane resistivity (≈16,000 ohms-cm~2) and capacitance (≈0.8 μF/cm~2) and the spatial distribution of L4-L2/3 synaptic contacts. The average peak conductance per L4 synaptic contact is 0.26 nS for the α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid and 0.2 nS for NMDA receptors. The in vivo voltage response for current steps was then used to calibrate the model for in vivo conditions in the Down state. Consequently, the effect of a single whisker deflection was modeled by converging, on average, 350 ± 20 L4 axons onto the modeled L2/3 pyramidal cell. Based on values of synaptic conductance, the spatial distribution of L4 synapses on L2/3 den-drites, and the average in vivo spiking probability of L4 spiny neurons, the model predicts that the feed-forward L4-L2/3 connection on its own does not fire the L2/3 neuron. With a broader distribution in the number of L4 neurons or with slight synchrony among them, the L2/3 model does spike with low probability.
机译:我们报告了建设新的皮质列的计算机模型的一个步骤,重点放在大鼠桶皮层中的第4层(L4)刺神经元和L2 / 3锥体细胞之间的突触连接。它首先基于从体外记录中突触连接的L4-L2 / 3神经元对的详细形态和功能表征,其次基于体内L2 / 3锥体细胞对电流脉冲和晶须偏转的电压响应的体内记录。体外数据和详细的L2 / 3锥体细胞区室模型使我们能够提取其比膜电阻率(≈16,000ohms-cm〜2)和电容(≈0.8μF/ cm〜2)以及L4-L2的空间分布/ 3突触接触。对于α-氨基-3-羟基-5-甲基-5-甲基-4-异恶唑丙酸,每个L4突触接触的平均峰值电导为0.26 nS,对于NMDA受体为0.2 nS。然后将当前步骤的体内电压响应用于在Down状态下针对体内条件校准模型。因此,通过将平均350±20个L4轴突收敛到建模的L2 / 3锥体细胞上,对单晶须偏转的影响进行了建模。基于突触电导值,L2 / 3树突上L4突触的空间分布以及L4刺神经元的体内平均加标概率,该模型可以预测前馈L4-L2 / 3连接是独立的不会激发L2 / 3神经元。 L2 / 3模型的L4神经元数量分布较宽或彼此之间具有较小的同步性,因此其尖峰概率较低。

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