连贯皮层反应的发展反映了前馈输入的可辨别性增强及其与循环回路的一致性。

IF 15 1区 医学 Q1 NEUROSCIENCES
Augusto Abel Lempel, Sigrid Trägenap, Clara Tepohl, Matthias Kaschube, David Fitzpatrick
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引用次数: 0

摘要

感觉皮质区通过将刺激驱动的输入转化为可靠的活动模式来指导行为。在视觉皮层中,被相同边缘方向激活的第4层(L4)神经元为共享强循环连接的第2/3层(L2/3)模块提供前馈输入。这种对齐有助于选择性放大,驱动可靠的、模块化的方向表示,但它是如何发展的仍不清楚。通过电生理和钙成像,我们发现在视觉幼稚的动物中,L4-L2/3的协同作用缺乏定向特异性。其中一个影响因素是L4的定向辨别能力较低,随着经验的增加而改善。然而,计算模型表明,错位的前馈-循环相互作用也起着关键作用,并预测了持续L2/3反应的调节动力学的发育变化,我们用全细胞记录证实了这一点。总之,我们的研究提供了证据,证明L4前馈输入的增强可辨析性及其与经验后反复出现的L2/3相互作用的一致性有助于发展具有层-颞叶一致性的可靠感觉表征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of coherent cortical responses reflects increased discriminability of feedforward inputs and their alignment with recurrent circuits.

Sensory cortical areas guide behavior by transforming stimulus-driven inputs into reliable activity patterns. In the visual cortex, layer 4 (L4) neurons activated by the same edge orientation provide feedforward input to layers 2/3 (L2/3) modules sharing strong recurrent connections. This alignment facilitates selective amplification, driving a reliable, modular representation of orientation, but how it develops remains unclear. Using electrophysiology and calcium imaging, we find that in visually naive animals, L4-L2/3 coactivity lacks orientation specificity. One contributing factor is low orientation discriminability in L4, which improves with experience. However, computational modeling indicates that misaligned feedforward-recurrent interactions also play a critical role and predict developmental changes in tuning dynamics of sustained L2/3 responses, which we confirm with whole-cell recordings. Altogether, our study provides evidence that enhanced discriminability of L4 feedforward inputs and their alignment with recurrent L2/3 interactions following experience contribute to the development of reliable sensory representations with laminar-temporal coherence.

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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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