Anatomically resolved oscillatory bursts reveal dynamic motifs of thalamocortical activity during naturalistic stimulus viewing.

IF 14.7 1区 医学 Q1 NEUROSCIENCES
Lukas Sebastian Meyerolbersleben, Anton Sirota, Laura Busse
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引用次数: 0

Abstract

Natural vision requires circuit mechanisms which process complex spatiotemporal stimulus features in parallel. In the mammalian forebrain, one signature of circuit activation is fast oscillatory dynamics, reflected in the local field potential (LFP). Using data from the Allen Neuropixels Visual Coding project, we show that local visual features in naturalistic stimuli induce in mouse primary visual cortex (V1) retinotopically specific oscillations in various frequency bands and V1 layers. Specifically, layer 4 (L4) narrowband gamma was linked to luminance, low-gamma to optic flow, and L4/L5 epsilon oscillations to contrast. These feature-specific oscillations were associated with distinct translaminar spike-phase coupling patterns, which were conserved across a range of stimuli containing the relevant visual features, suggesting that they might constitute feature-specific circuit motifs. Our findings highlight visually induced fast oscillations as markers of dynamic circuit motifs, which may support differential and multiplexed coding of complex visual input and thalamocortical information propagation.

解剖解决振荡爆发揭示动态动机丘脑皮质活动在自然刺激观看。
自然视觉需要并行处理复杂时空刺激特征的神经回路机制。在哺乳动物前脑中,电路激活的一个特征是快速振荡动力学,反映在局部场电位(LFP)上。利用Allen神经像素视觉编码项目的数据,我们发现自然刺激中的局部视觉特征诱导小鼠初级视觉皮层(V1)在不同频带和V1层的视网膜特异性振荡。具体来说,第4层(L4)窄带伽马与亮度有关,低伽马与光流有关,L4/L5的epsilon振荡与对比度有关。这些特征特异性振荡与不同的跨层流峰相耦合模式有关,这种模式在包含相关视觉特征的一系列刺激中都是保守的,这表明它们可能构成了特征特异性电路基序。我们的研究结果强调了视觉诱导的快速振荡作为动态电路基序的标记,这可能支持复杂视觉输入和丘脑皮质信息传播的差异和多路编码。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neuron
Neuron 医学-神经科学
CiteScore
24.50
自引率
3.10%
发文量
382
审稿时长
1 months
期刊介绍: Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.
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