Topographic correspondence between retinotopic and whisker somatosensory map in mouse higher visual area and its development.

IF 3 3区 医学 Q2 NEUROSCIENCES
Frontiers in Neural Circuits Pub Date : 2025-09-02 eCollection Date: 2025-01-01 DOI:10.3389/fncir.2025.1552130
Hanaka Matsumoto, Tomonari Murakami, Kenichi Ohki
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Abstract

Aligning the topography maps of different sensory modalities in the brain is considered to be important for the unified perception of multiple sensory modalities. In mice, the superior colliculus receives both visual and whisker-related somatosensory information with the topographical correspondence between retinotopy and somatotopy. However, it remains unclear whether topographical correspondence between retinotopy and whisker somatotopy exists in the higher association cortex, and if so, how this functional organization is formed during development. Here, we conducted wide-field calcium imaging and revealed retinotopic and somatotopic correspondence in the rostrolateral area (RL), one of the higher visual areas. The retinotopic map demonstrates that RL is divided into two distinct subregions, anterior and posterior parts of RL (RLa and RLp). We further found a rough topographic correspondence between retinotopy and whisker somatotopy only in RLa, but not in RLp, Lastly, to test whether this topographic correspondence exists before eye-opening, we performed functional connectivity analysis of spontaneous cortical activity recorded from developing mice. We discovered that the topographical correspondence between retinotopy-like and somatotopy-like structures in RLa already existed before eye-opening, on postnatal day 10-11. Because spatially corresponding multisensory inputs are likely quite weak before eye-opening, these results in developing mice suggest that the initial formation of topographic correspondence between retinotopy and whisker somatotopy in the higher association cortex does not depend on spatially corresponding multisensory input experiences.

小鼠高视区视网膜异位与须状体感图的地形对应关系及其发育。
对大脑中不同感觉模态的地形图进行对齐,对于多感觉模态的统一感知具有重要意义。在小鼠中,上丘同时接收视觉和须相关的体感信息,并具有视网膜切除和躯体切除之间的地形对应关系。然而,目前尚不清楚在高级联合皮层中是否存在视网膜切除和须体切除之间的地形对应关系,如果存在,这种功能组织在发育过程中是如何形成的。在这里,我们进行了宽视场钙显像,发现了高视觉区之一的前外侧区(RL)的视网膜定位和体位对应。视网膜定位图显示RL分为两个不同的亚区,RL的前部和后部(RLa和RLp)。我们进一步发现视网膜切除和须体切除之间仅在RLa中存在大致的地形对应关系,而在RLp中没有。最后,为了测试这种地形对应是否存在于睁眼之前,我们对发育小鼠的自发皮层活动进行了功能连接分析。我们发现视网膜样结构和体样结构之间的地形对应在睁眼之前,即出生后10-11天已经存在。由于空间上对应的多感觉输入在睁眼前可能相当弱,这些在发育中的小鼠身上的结果表明,视网膜切除和须体切除在高级关联皮层的初始地形对应的形成并不依赖于空间上对应的多感觉输入体验。
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来源期刊
CiteScore
6.00
自引率
5.70%
发文量
135
审稿时长
4-8 weeks
期刊介绍: Frontiers in Neural Circuits publishes rigorously peer-reviewed research on the emergent properties of neural circuits - the elementary modules of the brain. Specialty Chief Editors Takao K. Hensch and Edward Ruthazer at Harvard University and McGill University respectively, are supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics and the public worldwide. Frontiers in Neural Circuits launched in 2011 with great success and remains a "central watering hole" for research in neural circuits, serving the community worldwide to share data, ideas and inspiration. Articles revealing the anatomy, physiology, development or function of any neural circuitry in any species (from sponges to humans) are welcome. Our common thread seeks the computational strategies used by different circuits to link their structure with function (perceptual, motor, or internal), the general rules by which they operate, and how their particular designs lead to the emergence of complex properties and behaviors. Submissions focused on synaptic, cellular and connectivity principles in neural microcircuits using multidisciplinary approaches, especially newer molecular, developmental and genetic tools, are encouraged. Studies with an evolutionary perspective to better understand how circuit design and capabilities evolved to produce progressively more complex properties and behaviors are especially welcome. The journal is further interested in research revealing how plasticity shapes the structural and functional architecture of neural circuits.
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