Single neurons and networks in the mouse claustrum integrate input from widespread cortical sources.

IF 6.4 1区 生物学 Q1 BIOLOGY
eLife Pub Date : 2025-07-16 DOI:10.7554/eLife.98002
Andrew M Shelton, David K Oliver, Ivan P Lazarte, Joachim S Grimstvedt, Ishaan Kapoor, Jake A Swann, Caitlin A Ashcroft, Simon N Williams, Niall Conway, Selma Tir, Amy Robinson, Stuart Peirson, Thomas Akam, Clifford G Kentros, Menno P Witter, Simon J B Butt, Adam Max Packer
{"title":"Single neurons and networks in the mouse claustrum integrate input from widespread cortical sources.","authors":"Andrew M Shelton, David K Oliver, Ivan P Lazarte, Joachim S Grimstvedt, Ishaan Kapoor, Jake A Swann, Caitlin A Ashcroft, Simon N Williams, Niall Conway, Selma Tir, Amy Robinson, Stuart Peirson, Thomas Akam, Clifford G Kentros, Menno P Witter, Simon J B Butt, Adam Max Packer","doi":"10.7554/eLife.98002","DOIUrl":null,"url":null,"abstract":"<p><p>The claustrum is thought to be one of the most highly interconnected forebrain structures, but its organizing principles have yet to be fully explored at the level of single neurons. Here, we investigated the identity, connectivity, and activity of identified claustrum neurons in <i>Mus musculus</i> to understand how the structure's unique convergence of input and divergence of output support binding information streams. We found that neurons in the claustrum communicate with each other across efferent projection-defined modules which were differentially innervated by sensory and frontal cortical areas. Individual claustrum neurons were responsive to inputs from more than one cortical region in a cell-type and projection-specific manner, particularly between areas of frontal cortex. In vivo imaging of claustrum axons revealed responses to both unimodal and multimodal sensory stimuli. Finally, chronic claustrum silencing specifically reduced animals' sensitivity to multimodal stimuli. These findings support the view that the claustrum is a fundamentally integrative structure, consolidating information from around the cortex and redistributing it following local computations.</p>","PeriodicalId":11640,"journal":{"name":"eLife","volume":"13 ","pages":""},"PeriodicalIF":6.4000,"publicationDate":"2025-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"eLife","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.7554/eLife.98002","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The claustrum is thought to be one of the most highly interconnected forebrain structures, but its organizing principles have yet to be fully explored at the level of single neurons. Here, we investigated the identity, connectivity, and activity of identified claustrum neurons in Mus musculus to understand how the structure's unique convergence of input and divergence of output support binding information streams. We found that neurons in the claustrum communicate with each other across efferent projection-defined modules which were differentially innervated by sensory and frontal cortical areas. Individual claustrum neurons were responsive to inputs from more than one cortical region in a cell-type and projection-specific manner, particularly between areas of frontal cortex. In vivo imaging of claustrum axons revealed responses to both unimodal and multimodal sensory stimuli. Finally, chronic claustrum silencing specifically reduced animals' sensitivity to multimodal stimuli. These findings support the view that the claustrum is a fundamentally integrative structure, consolidating information from around the cortex and redistributing it following local computations.

小鼠屏状体中的单个神经元和网络整合来自广泛皮层来源的输入。
屏状体被认为是前脑中相互联系最紧密的结构之一,但其组织原理尚未在单个神经元的水平上得到充分的探索。在这里,我们研究了小家鼠中已识别的屏状体神经元的身份、连通性和活性,以了解该结构独特的输入收敛和输出发散如何支持绑定信息流。我们发现屏状体中的神经元通过不同的投射定义模块相互交流,这些模块由感觉和额叶皮质区不同的神经支配。单个屏状体神经元以细胞类型和投射特异性的方式对来自多个皮层区域的输入作出反应,特别是在额叶皮层区域之间。屏状体轴突的体内成像显示了对单峰和多峰感觉刺激的反应。最后,慢性屏状核沉默特别降低了动物对多模态刺激的敏感性。这些发现支持了屏状体是一个从根本上整合的结构的观点,它整合来自皮层周围的信息,并根据局部计算重新分配信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信