Astrocyte-secreted cues promote neural maturation and augment activity in human forebrain organoids

IF 15.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Nature Communications Pub Date : 2025-03-23 DOI:10.1038/s41467-025-58295-3
Honghui Zheng, Yilin Feng, Jiyuan Tang, Feifei Yu, Zitian Wang, Jiani Xu, Cheng Hai, Mingyue Jiang, Yifan Cheng, Zhicheng Shao, Ning Ma, Peter E. Lobie, Shaohua Ma
{"title":"Astrocyte-secreted cues promote neural maturation and augment activity in human forebrain organoids","authors":"Honghui Zheng, Yilin Feng, Jiyuan Tang, Feifei Yu, Zitian Wang, Jiani Xu, Cheng Hai, Mingyue Jiang, Yifan Cheng, Zhicheng Shao, Ning Ma, Peter E. Lobie, Shaohua Ma","doi":"10.1038/s41467-025-58295-3","DOIUrl":null,"url":null,"abstract":"<p>Brain organoids have been proposed as suitable human brain model candidates for a variety of applications. However, the lack of appropriate maturation limits the transferability of such functional tools. Here, we present a method to facilitate neuronal maturation by integrating astrocyte-secreted factors into hPSC-derived 2D and 3D neural culture systems. We demonstrate that protein- and nutrient-enriched astrocyte-conditioned medium (ACM) accelerates neuronal differentiation with enlarged neuronal layer and the overproduction of deep-layer cortical neurons. We captured the elevated changes in the functional activity of neuronal networks within ACM-treated organoids using comprehensive electrophysiological recordings. Furthermore, astrocyte-secreted cues can induce lipid droplet accumulation in neural cultures, offering protective effects in neural differentiation to withstand cellular stress. Together, these data indicate the potential of astrocyte secretions to promote neural maturation.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"17 1","pages":""},"PeriodicalIF":15.7000,"publicationDate":"2025-03-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-025-58295-3","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Brain organoids have been proposed as suitable human brain model candidates for a variety of applications. However, the lack of appropriate maturation limits the transferability of such functional tools. Here, we present a method to facilitate neuronal maturation by integrating astrocyte-secreted factors into hPSC-derived 2D and 3D neural culture systems. We demonstrate that protein- and nutrient-enriched astrocyte-conditioned medium (ACM) accelerates neuronal differentiation with enlarged neuronal layer and the overproduction of deep-layer cortical neurons. We captured the elevated changes in the functional activity of neuronal networks within ACM-treated organoids using comprehensive electrophysiological recordings. Furthermore, astrocyte-secreted cues can induce lipid droplet accumulation in neural cultures, offering protective effects in neural differentiation to withstand cellular stress. Together, these data indicate the potential of astrocyte secretions to promote neural maturation.

Abstract Image

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
星形胶质细胞分泌的线索促进人类前脑器官组织的神经成熟并增强其活性
脑类器官已被提出作为合适的人脑模型候选人的各种应用。然而,缺乏适当的成熟度限制了这些功能工具的可转移性。在这里,我们提出了一种通过将星形胶质细胞分泌因子整合到hpsc衍生的2D和3D神经培养系统中来促进神经元成熟的方法。我们证明,富含蛋白质和营养的星形胶质细胞条件培养基(ACM)加速神经元分化,扩大神经元层和深层皮层神经元的过量生产。我们利用全面的电生理记录捕捉到了acm处理的类器官中神经元网络功能活动的升高变化。此外,星形胶质细胞分泌的线索可以诱导神经培养物中的脂滴积累,为神经分化抵御细胞应激提供保护作用。总之,这些数据表明星形胶质细胞分泌物促进神经成熟的潜力。
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
Nature Communications
Nature Communications Biological Science Disciplines-
CiteScore
24.90
自引率
2.40%
发文量
6928
审稿时长
3.7 months
期刊介绍: Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.
期刊最新文献
Electrochemical tyrosine-click bioconjugation enables multiplexed cytokine sensing and immunoprofiling in native serum. Carbene-catalyzed double esterification enables enantioselective conformational self-locking of pillar[5]arenes. Structural basis of the cyclin Y/14-3-3 protein-mediated activation of CDK16. International testing and refinement of AI algorithms predicting acute leukemia subtypes from routine laboratory data. Transcriptional competence defines the heterochromatin nucleating potential of isolated MSR units.
×
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:604180095
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