Emergence of a brainstem somatosensory tonotopic map for substrate vibration

IF 21.2 1区 医学 Q1 NEUROSCIENCES
Kuo-Sheng Lee, Alastair J. Loutit, Dominica de Thomas Wagner, Mark Sanders, Daniel Huber
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引用次数: 0

Abstract

Perceiving substrate-borne vibrations is a fundamental component of tactile perception. How location (somatotopy) and frequency tuning (tonotopy) of vibrations are integratively processed is poorly understood. Here we addressed this question using in vivo electrophysiology and two-photon calcium imaging along the dorsal column–medial lemniscal pathway. We found that both frequency and location are organized into structured maps in the dorsal column nuclei (DCN). Both maps are intimately related at the fine spatial scale, with parallel map gradients that are consistent across the depth of the DCN and preserved along the ascending pathway. The tonotopic map only partially reflects the distribution of end organs in the skin and deep tissue; instead, the emergence of the fine-scale tonotopy is due to the selective dendritic sampling from axonal afferents, already at the first synaptic relay. We conclude that DCN neural circuits are key to the emergence of these two fine-scale topographical organizations in early somatosensory pathways.

Abstract Image

针对底物振动的脑干体感色调图谱的出现
感知基底振动是触觉感知的基本组成部分。人们对振动的位置(体感)和频率调谐(调谐)是如何综合处理的还知之甚少。在这里,我们利用背柱-内侧半月板通路的活体电生理学和双光子钙成像来解决这个问题。我们发现,在背柱核(DCN)中,频率和位置都被组织成结构图。这两种图谱在精细空间尺度上密切相关,其平行图谱梯度在整个背柱核深度上一致,并沿上升通路保留。音调图仅部分反映了皮肤和深层组织中末梢器官的分布;相反,细尺度音调图的出现是由于轴突传入的选择性树突取样,在第一次突触中继时就已出现。我们的结论是,DCN神经回路是早期躯体感觉通路出现这两种精细尺度地形组织的关键。
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来源期刊
Nature neuroscience
Nature neuroscience 医学-神经科学
CiteScore
38.60
自引率
1.20%
发文量
212
审稿时长
1 months
期刊介绍: Nature Neuroscience, a multidisciplinary journal, publishes papers of the utmost quality and significance across all realms of neuroscience. The editors welcome contributions spanning molecular, cellular, systems, and cognitive neuroscience, along with psychophysics, computational modeling, and nervous system disorders. While no area is off-limits, studies offering fundamental insights into nervous system function receive priority. The journal offers high visibility to both readers and authors, fostering interdisciplinary communication and accessibility to a broad audience. It maintains high standards of copy editing and production, rigorous peer review, rapid publication, and operates independently from academic societies and other vested interests. In addition to primary research, Nature Neuroscience features news and views, reviews, editorials, commentaries, perspectives, book reviews, and correspondence, aiming to serve as the voice of the global neuroscience community.
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