识别小鼠胡须 S1 和 S2 皮层之间信息传递的发育开关

IF 3.2 3区 经济学 Q1 ECONOMICS Economics of Innovation and New Technology Pub Date : 2022-06-01 Epub Date: 2022-05-02 DOI:10.1523/JNEUROSCI.2246-21.2022
Linbi Cai, Jenq-Wei Yang, Chia-Fang Wang, Shen-Ju Chou, Heiko J Luhmann, Theofanis Karayannis
{"title":"识别小鼠胡须 S1 和 S2 皮层之间信息传递的发育开关","authors":"Linbi Cai, Jenq-Wei Yang, Chia-Fang Wang, Shen-Ju Chou, Heiko J Luhmann, Theofanis Karayannis","doi":"10.1523/JNEUROSCI.2246-21.2022","DOIUrl":null,"url":null,"abstract":"<p><p>The whiskers of rodents are a key sensory organ that provides critical tactile information for animal navigation and object exploration throughout life. Previous work has explored the developmental sensory-driven activation of the primary sensory cortex processing whisker information (wS1), also called barrel cortex. This body of work has shown that the barrel cortex is already activated by sensory stimuli during the first postnatal week. However, it is currently unknown when over the course of development these stimuli begin being processed by higher-order cortical areas, such as secondary whisker somatosensory area (wS2). Here we investigate the developmental engagement of wS2 by whisker stimuli and the emergence of corticocortical communication from wS1 to wS2. Using <i>in vivo</i> wide-field imaging and multielectrode recordings in control and conditional KO mice of either sex with thalamocortical innervation defects, we find that wS1 and wS2 are able to process bottom-up information coming from the thalamus from birth. We also identify that it is only at the end of the first postnatal week that wS1 begins to provide functional excitation into wS2, switching to more inhibitory actions after the second postnatal week. Therefore, we have uncovered a developmental window when information transfer between wS1 and wS2 reaches mature function.<b>SIGNIFICANCE STATEMENT</b> At the end of the first postnatal week, the primary whisker somatosensory area starts providing excitatory input to the secondary whisker somatosensory area 2. This excitatory drive weakens during the second postnatal week and switches to inhibition in the adult.</p>","PeriodicalId":51485,"journal":{"name":"Economics of Innovation and New Technology","volume":"13 1","pages":"4435-4448"},"PeriodicalIF":3.2000,"publicationDate":"2022-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9172289/pdf/","citationCount":"0","resultStr":"{\"title\":\"Identification of a Developmental Switch in Information Transfer between Whisker S1 and S2 Cortex in Mice.\",\"authors\":\"Linbi Cai, Jenq-Wei Yang, Chia-Fang Wang, Shen-Ju Chou, Heiko J Luhmann, Theofanis Karayannis\",\"doi\":\"10.1523/JNEUROSCI.2246-21.2022\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The whiskers of rodents are a key sensory organ that provides critical tactile information for animal navigation and object exploration throughout life. Previous work has explored the developmental sensory-driven activation of the primary sensory cortex processing whisker information (wS1), also called barrel cortex. This body of work has shown that the barrel cortex is already activated by sensory stimuli during the first postnatal week. However, it is currently unknown when over the course of development these stimuli begin being processed by higher-order cortical areas, such as secondary whisker somatosensory area (wS2). Here we investigate the developmental engagement of wS2 by whisker stimuli and the emergence of corticocortical communication from wS1 to wS2. Using <i>in vivo</i> wide-field imaging and multielectrode recordings in control and conditional KO mice of either sex with thalamocortical innervation defects, we find that wS1 and wS2 are able to process bottom-up information coming from the thalamus from birth. We also identify that it is only at the end of the first postnatal week that wS1 begins to provide functional excitation into wS2, switching to more inhibitory actions after the second postnatal week. Therefore, we have uncovered a developmental window when information transfer between wS1 and wS2 reaches mature function.<b>SIGNIFICANCE STATEMENT</b> At the end of the first postnatal week, the primary whisker somatosensory area starts providing excitatory input to the secondary whisker somatosensory area 2. This excitatory drive weakens during the second postnatal week and switches to inhibition in the adult.</p>\",\"PeriodicalId\":51485,\"journal\":{\"name\":\"Economics of Innovation and New Technology\",\"volume\":\"13 1\",\"pages\":\"4435-4448\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2022-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9172289/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Economics of Innovation and New Technology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1523/JNEUROSCI.2246-21.2022\",\"RegionNum\":3,\"RegionCategory\":\"经济学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2022/5/2 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"ECONOMICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Economics of Innovation and New Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1523/JNEUROSCI.2246-21.2022","RegionNum":3,"RegionCategory":"经济学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/5/2 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"ECONOMICS","Score":null,"Total":0}
引用次数: 0

摘要

啮齿类动物的胡须是一个关键的感觉器官,它为动物一生的导航和物体探索提供关键的触觉信息。以往的研究工作探索了处理胡须信息的初级感觉皮层(wS1)(也称桶状皮层)在发育过程中由感觉驱动的激活。这些研究表明,桶状皮层在出生后第一周就已经被感官刺激激活。然而,在发育过程中,这些刺激何时开始由更高阶的皮层区域(如次级须体感区(wS2))进行处理,目前尚不清楚。在此,我们研究了胡须刺激对 wS2 的发育参与,以及从 wS1 到 wS2 的皮质通信的出现。通过对丘脑皮层神经支配缺陷的对照组小鼠和条件性 KO 小鼠进行体内宽场成像和多电极记录,我们发现 wS1 和 wS2 从出生起就能处理来自丘脑的自下而上的信息。我们还发现,只有在出生后第一周结束时,wS1 才开始向 wS2 提供功能性兴奋,而在出生后第二周之后,则转为更多的抑制作用。因此,我们发现了 wS1 和 wS2 之间的信息传递达到成熟功能的发育窗口。意义声明 在出生后第一周末,初级胡须体感区开始向次级胡须体感区 2 提供兴奋性输入。这种兴奋驱动力在出生后第二周逐渐减弱,成年后转为抑制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Identification of a Developmental Switch in Information Transfer between Whisker S1 and S2 Cortex in Mice.

The whiskers of rodents are a key sensory organ that provides critical tactile information for animal navigation and object exploration throughout life. Previous work has explored the developmental sensory-driven activation of the primary sensory cortex processing whisker information (wS1), also called barrel cortex. This body of work has shown that the barrel cortex is already activated by sensory stimuli during the first postnatal week. However, it is currently unknown when over the course of development these stimuli begin being processed by higher-order cortical areas, such as secondary whisker somatosensory area (wS2). Here we investigate the developmental engagement of wS2 by whisker stimuli and the emergence of corticocortical communication from wS1 to wS2. Using in vivo wide-field imaging and multielectrode recordings in control and conditional KO mice of either sex with thalamocortical innervation defects, we find that wS1 and wS2 are able to process bottom-up information coming from the thalamus from birth. We also identify that it is only at the end of the first postnatal week that wS1 begins to provide functional excitation into wS2, switching to more inhibitory actions after the second postnatal week. Therefore, we have uncovered a developmental window when information transfer between wS1 and wS2 reaches mature function.SIGNIFICANCE STATEMENT At the end of the first postnatal week, the primary whisker somatosensory area starts providing excitatory input to the secondary whisker somatosensory area 2. This excitatory drive weakens during the second postnatal week and switches to inhibition in the adult.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
7.20
自引率
3.00%
发文量
30
期刊介绍: Economics of Innovation and New Technology is devoted to the theoretical and empirical analysis of the determinants and effects of innovation, new technology and technological knowledge. The journal aims to provide a bridge between different strands of literature and different contributions of economic theory and empirical economics. This bridge is built in two ways. First, by encouraging empirical research (including case studies, econometric work and historical research), evaluating existing economic theory, and suggesting appropriate directions for future effort in theoretical work. Second, by exploring ways of applying and testing existing areas of theory to the economics of innovation and new technology, and ways of using theoretical insights to inform data collection and other empirical research. The journal welcomes contributions across a wide range of issues concerned with innovation, including: the generation of new technological knowledge, innovation in product markets, process innovation, patenting, adoption, diffusion, innovation and technology policy, international competitiveness, standardization and network externalities, innovation and growth, technology transfer, innovation and market structure, innovation and the environment, and across a broad range of economic activity not just in ‘high technology’ areas. The journal is open to a variety of methodological approaches ranging from case studies to econometric exercises with sound theoretical modelling, empirical evidence both longitudinal and cross-sectional about technologies, regions, firms, industries and countries.
期刊最新文献
Digital transition in a turbulent world: European regional growth opportunities in 17 years' time Patent infringement litigation, executive team risk appetite and corporate innovation Synergistic governance and innovation: the positive effect of cross-holding partners Do scarce resource inputs promote or reduce patent values and innovation? A game theory approach R&D lags in economic models
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1