工程皮质网络:一个开放的平台,控制人类电路的形成和突触分析在体外。

IF 9.6 2区 医学 Q1 ENGINEERING, BIOMEDICAL
Pacharaporn Suklai, Taylor Minckley, Cathleen Hagemann, Karolina Faber, Rosalind Norkett, Ludovica Guetta, Kelly O'Toole, Bethany Geary, Michael J Devine, Andrea Serio
{"title":"工程皮质网络:一个开放的平台,控制人类电路的形成和突触分析在体外。","authors":"Pacharaporn Suklai, Taylor Minckley, Cathleen Hagemann, Karolina Faber, Rosalind Norkett, Ludovica Guetta, Kelly O'Toole, Bethany Geary, Michael J Devine, Andrea Serio","doi":"10.1002/adhm.202500857","DOIUrl":null,"url":null,"abstract":"<p><p>Neuronal circuits are organized by specific connections between neuron types across various brain regions. Understanding how these circuits form is crucial for uncovering the mechanisms behind circuit-related dysfunction in brain diseases. Human-induced pluripotent stem cell (iPSC) models enable the study of the molecular and cellular processes underlying neuronal networks, but their lack of precise architecture limits the investigation of specific neuronal interactions and activity-dependent processes. Microfluidic technologies offer structural control but are confined by closed systems that restrict 3D network integration, scalability, and cell retrieval. To overcome these challenges, we developed an open cortical network platform that integrates iPSC-derived cortical neurons with bioengineering techniques. Using a polydimethylsiloxane-based microgroove topography and a cell plating guide, we created \"neuronal nodes\" that facilitate flexible circuit construction in an open system. This design allows optogenetic control of neural activity and flexible network modifications, including cellular composition, neurite directionality, and synapse formation. The open, large-scale design allows neuronal material retrieval, supporting multi-level analyses of cortical circuits, such as proteomics. This platform represents a valuable tool for investigating neuronal network development and function, providing opportunities for study into both normal and pathological states, including molecular changes associated with connectivity loss in brain diseases.</p>","PeriodicalId":113,"journal":{"name":"Advanced Healthcare Materials","volume":" ","pages":"e00857"},"PeriodicalIF":9.6000,"publicationDate":"2025-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Engineering Cortical Networks: An Open Platform for Controlled Human Circuit Formation and Synaptic Analysis In Vitro.\",\"authors\":\"Pacharaporn Suklai, Taylor Minckley, Cathleen Hagemann, Karolina Faber, Rosalind Norkett, Ludovica Guetta, Kelly O'Toole, Bethany Geary, Michael J Devine, Andrea Serio\",\"doi\":\"10.1002/adhm.202500857\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Neuronal circuits are organized by specific connections between neuron types across various brain regions. Understanding how these circuits form is crucial for uncovering the mechanisms behind circuit-related dysfunction in brain diseases. Human-induced pluripotent stem cell (iPSC) models enable the study of the molecular and cellular processes underlying neuronal networks, but their lack of precise architecture limits the investigation of specific neuronal interactions and activity-dependent processes. Microfluidic technologies offer structural control but are confined by closed systems that restrict 3D network integration, scalability, and cell retrieval. To overcome these challenges, we developed an open cortical network platform that integrates iPSC-derived cortical neurons with bioengineering techniques. Using a polydimethylsiloxane-based microgroove topography and a cell plating guide, we created \\\"neuronal nodes\\\" that facilitate flexible circuit construction in an open system. This design allows optogenetic control of neural activity and flexible network modifications, including cellular composition, neurite directionality, and synapse formation. The open, large-scale design allows neuronal material retrieval, supporting multi-level analyses of cortical circuits, such as proteomics. This platform represents a valuable tool for investigating neuronal network development and function, providing opportunities for study into both normal and pathological states, including molecular changes associated with connectivity loss in brain diseases.</p>\",\"PeriodicalId\":113,\"journal\":{\"name\":\"Advanced Healthcare Materials\",\"volume\":\" \",\"pages\":\"e00857\"},\"PeriodicalIF\":9.6000,\"publicationDate\":\"2025-10-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Healthcare Materials\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1002/adhm.202500857\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, BIOMEDICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Healthcare Materials","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1002/adhm.202500857","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
引用次数: 0

摘要

神经元回路是由大脑不同区域的神经元类型之间的特定连接组织起来的。了解这些回路如何形成对于揭示脑疾病中回路相关功能障碍背后的机制至关重要。人类诱导的多能干细胞(iPSC)模型能够研究神经网络背后的分子和细胞过程,但它们缺乏精确的结构限制了对特定神经元相互作用和活动依赖过程的研究。微流控技术提供结构控制,但受到封闭系统的限制,限制了3D网络集成、可扩展性和细胞检索。为了克服这些挑战,我们开发了一个开放的皮质网络平台,将ipsc衍生的皮质神经元与生物工程技术相结合。使用基于聚二甲基硅氧烷的微槽形貌和细胞电镀指南,我们创建了“神经元节点”,促进了开放系统中柔性电路的构建。这种设计允许光遗传学控制神经活动和灵活的网络修改,包括细胞组成、神经突方向性和突触形成。开放、大规模的设计允许神经元材料检索,支持皮层回路的多层次分析,如蛋白质组学。这个平台是研究神经网络发育和功能的一个有价值的工具,为研究正常和病理状态提供了机会,包括与脑疾病中连通性丧失相关的分子变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Engineering Cortical Networks: An Open Platform for Controlled Human Circuit Formation and Synaptic Analysis In Vitro.

Neuronal circuits are organized by specific connections between neuron types across various brain regions. Understanding how these circuits form is crucial for uncovering the mechanisms behind circuit-related dysfunction in brain diseases. Human-induced pluripotent stem cell (iPSC) models enable the study of the molecular and cellular processes underlying neuronal networks, but their lack of precise architecture limits the investigation of specific neuronal interactions and activity-dependent processes. Microfluidic technologies offer structural control but are confined by closed systems that restrict 3D network integration, scalability, and cell retrieval. To overcome these challenges, we developed an open cortical network platform that integrates iPSC-derived cortical neurons with bioengineering techniques. Using a polydimethylsiloxane-based microgroove topography and a cell plating guide, we created "neuronal nodes" that facilitate flexible circuit construction in an open system. This design allows optogenetic control of neural activity and flexible network modifications, including cellular composition, neurite directionality, and synapse formation. The open, large-scale design allows neuronal material retrieval, supporting multi-level analyses of cortical circuits, such as proteomics. This platform represents a valuable tool for investigating neuronal network development and function, providing opportunities for study into both normal and pathological states, including molecular changes associated with connectivity loss in brain diseases.

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
Advanced Healthcare Materials
Advanced Healthcare Materials 工程技术-生物材料
CiteScore
14.40
自引率
3.00%
发文量
600
审稿时长
1.8 months
期刊介绍: Advanced Healthcare Materials, a distinguished member of the esteemed Advanced portfolio, has been dedicated to disseminating cutting-edge research on materials, devices, and technologies for enhancing human well-being for over ten years. As a comprehensive journal, it encompasses a wide range of disciplines such as biomaterials, biointerfaces, nanomedicine and nanotechnology, tissue engineering, and regenerative medicine.
×
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