空间情境非均匀地调节初级视觉皮层的层间信息流

IF 14.7 1区 医学 Q1 NEUROSCIENCES
Xize Xu, Mitchell P Morton, Sachira Denagamage, Nyomi V Hudson, Anirvan S Nandy, Monika P Jadi
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引用次数: 0

摘要

我们的视觉体验是感觉层次中神经元集合协同活动的结果。然而,人们对物体的空间组织如何影响这种活动仍然知之甚少。我们研究了初级视觉皮层(V1)中的层间信息流如何受到孤立的视觉刺激或在已知会导致感知非均匀退化的空间配置中的侧翼刺激的影响。通过采用降维方法对特定层群进行同步记录,我们确定了皮层之间的信息传播是沿着结构稳定的通信子空间进行的。上下文刺激的空间配置会不同程度地调节层间通讯效率、前馈和有效反馈信号的平衡以及表层的上下文信号。值得注意的是,这些调节反映了知觉退化在空间上的不均匀性。我们的研究结果表明,V1 输出层中视网膜视图非均匀性皮层连接模型会影响感觉层次结构中的信息流。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spatial context non-uniformly modulates inter-laminar information flow in the primary visual cortex.

Our visual experience is a result of the concerted activity of neuronal ensembles in the sensory hierarchy. Yet, how the spatial organization of objects influences this activity remains poorly understood. We investigate how inter-laminar information flow within the primary visual cortex (V1) is affected by visual stimuli in isolation or with flankers at spatial configurations that are known to cause non-uniform degradation of perception. By employing dimensionality reduction approaches to simultaneous, layer-specific population recordings, we establish that information propagation between cortical layers occurs along a structurally stable communication subspace. The spatial configuration of contextual stimuli differentially modulates inter-laminar communication efficacy, the balance of feedforward and effective feedback signaling, and contextual signaling in the superficial layers. Remarkably, these modulations mirror the spatially non-uniform aspects of perceptual degradation. Our results suggest a model of retinotopically non-uniform cortical connectivity in the output layers of V1 that influences information flow in the sensory hierarchy.

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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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