Brain injury reactivates a developmental program driving genesis and integration of transient LGE-class interneurons.

IF 5.6 2区 医学 Q1 CELL & TISSUE ENGINEERING
Stem Cell Reports Pub Date : 2026-08-11 Epub Date: 2026-07-16 DOI:10.1016/j.stemcr.2026.103015
G Nato, M Fogli, N Marichal, V Cerrato, G Turrini, V Proserpio, I Ghia, G Zanotto, I Molineris, M Bergami, S Oliviero, P Peretto, B Berninger, A Buffo, F Luzzati
{"title":"Brain injury reactivates a developmental program driving genesis and integration of transient LGE-class interneurons.","authors":"G Nato, M Fogli, N Marichal, V Cerrato, G Turrini, V Proserpio, I Ghia, G Zanotto, I Molineris, M Bergami, S Oliviero, P Peretto, B Berninger, A Buffo, F Luzzati","doi":"10.1016/j.stemcr.2026.103015","DOIUrl":null,"url":null,"abstract":"<p><p>Brain lesions can unlock latent neurogenic potential in parenchymal astrocytes, but the identity of their neuronal progeny has remained unclear. Here, we show that neurons generated by striatal astrocytes after excitotoxic lesions are transient, yet reach advanced morphological and functional maturation and integrate into cortico-striatal-thalamic circuits. Single-cell RNA-seq mapping onto an embryonic reference revealed these cells are not fated to adult striatal neuron types but belong to the LGE-MEIS2/PAX6 interneuron class. Reanalysis of neuroblasts from cortical and striatal astrocytes after Notch abrogation revealed shared commitment of rostral telencephalic astrocytes to this class. Public spatial transcriptomics datasets revealed these cells are widely distributed throughout the mouse telencephalon during embryonic and postnatal development. Thus, unlike other vertebrates in which adult telencephalic astroglia preserve the potential to generate resident, regionally appropriate neuronal types, homologous mammalian cells converge on a specific transient neuron class, possibly representing a reservoir for circuit plasticity in adult life.</p>","PeriodicalId":21885,"journal":{"name":"Stem Cell Reports","volume":" ","pages":"103015"},"PeriodicalIF":5.6000,"publicationDate":"2026-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13476880/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Stem Cell Reports","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.stemcr.2026.103015","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/7/16 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CELL & TISSUE ENGINEERING","Score":null,"Total":0}
引用次数: 0

Abstract

Brain lesions can unlock latent neurogenic potential in parenchymal astrocytes, but the identity of their neuronal progeny has remained unclear. Here, we show that neurons generated by striatal astrocytes after excitotoxic lesions are transient, yet reach advanced morphological and functional maturation and integrate into cortico-striatal-thalamic circuits. Single-cell RNA-seq mapping onto an embryonic reference revealed these cells are not fated to adult striatal neuron types but belong to the LGE-MEIS2/PAX6 interneuron class. Reanalysis of neuroblasts from cortical and striatal astrocytes after Notch abrogation revealed shared commitment of rostral telencephalic astrocytes to this class. Public spatial transcriptomics datasets revealed these cells are widely distributed throughout the mouse telencephalon during embryonic and postnatal development. Thus, unlike other vertebrates in which adult telencephalic astroglia preserve the potential to generate resident, regionally appropriate neuronal types, homologous mammalian cells converge on a specific transient neuron class, possibly representing a reservoir for circuit plasticity in adult life.

脑损伤重新激活了一个发育程序,驱动瞬态大鼠级中间神经元的发生和整合。
脑损伤可以释放实质星形胶质细胞的潜在神经源性潜能,但其神经元后代的身份仍不清楚。本研究表明,纹状体星形胶质细胞在兴奋性毒性损伤后产生的神经元是短暂的,但在形态和功能上达到了高级成熟,并整合到皮质-纹状体-丘脑回路中。单细胞RNA-seq定位到胚胎参照物显示,这些细胞不是注定要成为成年纹状体神经元类型,而是属于LGE-MEIS2/PAX6中间神经元类。Notch缺失后对皮层和纹状体星形胶质细胞的神经母细胞的再分析显示,吻侧端脑星形胶质细胞也属于这一类。公共空间转录组学数据显示,这些细胞在胚胎和出生后发育期间广泛分布于小鼠端脑。因此,与其他脊椎动物不同,在其他脊椎动物中,成年端脑星形胶质细胞保留了产生常驻的、局部合适的神经元类型的潜力,同源哺乳动物细胞聚集在特定的瞬时神经元类别上,可能代表了成年生命中电路可塑性的储存库。
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
Stem Cell Reports
Stem Cell Reports CELL & TISSUE ENGINEERING-CELL BIOLOGY
CiteScore
10.50
自引率
1.70%
发文量
200
审稿时长
28 weeks
期刊介绍: Stem Cell Reports publishes high-quality, peer-reviewed research presenting conceptual or practical advances across the breadth of stem cell research and its applications to medicine. Our particular focus on shorter, single-point articles, timely publication, strong editorial decision-making and scientific input by leaders in the field and a "scoop protection" mechanism are reasons to submit your best papers.
×
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
小红书