Embryonically active piriform cortex neurons promote intracortical recurrent connectivity during development.

IF 14.7 1区 医学 Q1 NEUROSCIENCES Neuron Pub Date : 2024-09-04 Epub Date: 2024-07-03 DOI:10.1016/j.neuron.2024.06.007
David C Wang, Fernando Santos-Valencia, Jun H Song, Kevin M Franks, Liqun Luo
{"title":"Embryonically active piriform cortex neurons promote intracortical recurrent connectivity during development.","authors":"David C Wang, Fernando Santos-Valencia, Jun H Song, Kevin M Franks, Liqun Luo","doi":"10.1016/j.neuron.2024.06.007","DOIUrl":null,"url":null,"abstract":"<p><p>Neuronal activity plays a critical role in the maturation of circuits that propagate sensory information into the brain. How widely does early activity regulate circuit maturation across the developing brain? Here, we used targeted recombination in active populations (TRAP) to perform a brain-wide survey for prenatally active neurons in mice and identified the piriform cortex as an abundantly TRAPed region. Whole-cell recordings in neonatal slices revealed preferential interconnectivity within embryonically TRAPed piriform neurons and their enhanced synaptic connectivity with other piriform neurons. In vivo Neuropixels recordings in neonates demonstrated that embryonically TRAPed piriform neurons exhibit broad functional connectivity within piriform and lead spontaneous synchronized population activity during a transient neonatal period, when recurrent connectivity is strengthening. Selectively activating or silencing these neurons in neonates enhanced or suppressed recurrent synaptic strength, respectively. Thus, embryonically TRAPed piriform neurons represent an interconnected hub-like population whose activity promotes recurrent connectivity in early development.</p>","PeriodicalId":19313,"journal":{"name":"Neuron","volume":" ","pages":"2938-2954.e6"},"PeriodicalIF":14.7000,"publicationDate":"2024-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11377168/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuron","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.neuron.2024.06.007","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/3 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Neuronal activity plays a critical role in the maturation of circuits that propagate sensory information into the brain. How widely does early activity regulate circuit maturation across the developing brain? Here, we used targeted recombination in active populations (TRAP) to perform a brain-wide survey for prenatally active neurons in mice and identified the piriform cortex as an abundantly TRAPed region. Whole-cell recordings in neonatal slices revealed preferential interconnectivity within embryonically TRAPed piriform neurons and their enhanced synaptic connectivity with other piriform neurons. In vivo Neuropixels recordings in neonates demonstrated that embryonically TRAPed piriform neurons exhibit broad functional connectivity within piriform and lead spontaneous synchronized population activity during a transient neonatal period, when recurrent connectivity is strengthening. Selectively activating or silencing these neurons in neonates enhanced or suppressed recurrent synaptic strength, respectively. Thus, embryonically TRAPed piriform neurons represent an interconnected hub-like population whose activity promotes recurrent connectivity in early development.

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
胚胎期活跃的梨状皮层神经元在发育过程中促进了皮层内的循环连接。
神经元活动在将感官信息传播到大脑的电路成熟过程中起着至关重要的作用。早期活动对整个发育中大脑回路成熟的调节作用有多大?在这里,我们利用活跃群体中的定向重组(TRAP)对小鼠出生前活跃的神经元进行了全脑调查,发现梨状皮层是一个TRAP丰富的区域。新生儿切片的全细胞记录显示,胚胎TRAP化的梨状体神经元具有优先互联性,而且它们与其他梨状体神经元的突触连接也得到了增强。新生儿体内神经像素记录显示,胚胎TRAP化的梨状体神经元在梨状体内表现出广泛的功能连接性,并在新生儿的短暂时期内导致自发的同步群体活动,而这一时期的复发性连接性正在加强。选择性地激活或沉默这些神经元可分别增强或抑制新生儿的递归突触强度。因此,胚胎TRAP化的梨状体神经元代表了一个相互连接的枢纽样群体,其活动促进了早期发育中的递归连接。
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 去求助
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.
期刊最新文献
Meningeal neutrophil immune signaling influences behavioral adaptation following threat. Stability of cross-sensory input to primary somatosensory cortex across experience. Appoptosin-Mediated Caspase Cleavage of Tau Contributes to Progressive Supranuclear Palsy Pathogenesis. Network-wide risk convergence in gene co-expression identifies reproducible genetic hubs of schizophrenia risk. Failure in a population: Tauopathy disrupts homeostatic set-points in emergent dynamics despite stability in the constituent neurons.
×
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