Experience influences the refinement of feature selectivity in the mouse primary visual thalamus.

IF 14.7 1区 医学 Q1 NEUROSCIENCES
Neuron Pub Date : 2025-05-07 Epub Date: 2025-03-19 DOI:10.1016/j.neuron.2025.02.023
Takuma Sonoda, Céleste-Élise Stephany, Kaleb Kelley, Di Kang, Rui Wu, Meghna R Uzgare, Michela Fagiolini, Michael E Greenberg, Chinfei Chen
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引用次数: 0

Abstract

Neurons exhibit selectivity for specific features: a property essential for extracting and encoding relevant information in the environment. This feature selectivity is thought to be modifiable by experience at the level of the cortex. Here, we demonstrate that selective exposure to a feature during development can alter the population representation of that feature in the primary visual thalamus. This thalamic plasticity is not due to changes in corticothalamic inputs and is blocked in mutant mice that exhibit deficits in retinogeniculate refinement, suggesting that plasticity is a direct result of changes in feedforward connectivity. Notably, experience-dependent changes in thalamic feature selectivity also occur in adult animals, although these changes are transient, unlike in juvenile animals, where they are long lasting. These results reveal an unexpected degree of plasticity in the visual thalamus and show that salient environmental features can be encoded in thalamic circuits during a discrete developmental window.

经验影响小鼠初级视觉丘脑特征选择性的完善
神经元表现出对特定特征的选择性:这是提取和编码环境中相关信息所必需的属性。这种特征的选择性被认为是可以通过大脑皮层的经验来改变的。在这里,我们证明了在发育过程中选择性地暴露于一个特征可以改变该特征在初级视觉丘脑中的总体表征。这种丘脑可塑性不是由于皮质丘脑输入的变化,而是在视网膜原化细化缺陷的突变小鼠中被阻断,这表明可塑性是前馈连接变化的直接结果。值得注意的是,在成年动物中,丘脑特征选择性的经验依赖变化也会发生,尽管这些变化是短暂的,不像在幼年动物中,它们是持久的。这些结果揭示了视觉丘脑具有意想不到的可塑性,并表明在一个离散的发育窗口期间,显著的环境特征可以在丘脑回路中被编码。
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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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