• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

制造用于神经疾病建模和药物评估的均匀脑类器官

Manufacturing Uniform Cerebral Organoids for Neurological Disease Modeling and Drug Evaluation.

作者信息

Hong Hyowon, Jun Yesl, Yoon Sae-Bom, Park Seoyoon, Lee Jaemeun, Jang Jeong Woon, Nam Hye Jin, Cho Heeyeong

机构信息

Therapeutics & Biotechnology Division, Korea Research Institute of Chemical Technology, Daejeon, Republic of Korea.

Medicinal Chemistry and Pharmacology, University of Science and Technology, Daejeon, Republic of Korea.

出版信息

Biomater Res. 2024 Nov 6;28:0104. doi: 10.34133/bmr.0104. eCollection 2024.

DOI:10.34133/bmr.0104
PMID:39507522
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11538552/
Abstract

Human cerebral organoids are promising tools for investigating brain development and the pathogenesis underlying neurological disorders. To use organoids for drug effectiveness and safety screening, the organoids dispensed into each well must be prepared under precisely the same conditions as the cells. Despite decades of extensive research on approaches to improve organoid generation, various challenges remain, such as low yields and heterogeneity in size and differentiation both within and between batches. Here, we newly established uniform cerebral organoids (UCOs) derived from induced pluripotent stem cells by optimizing organoid size and performing real-time monitoring of telencephalic differentiation marker expression. These organoids exhibited morphological uniformity and consistent expression of during telencephalic differentiation, with high productivity. Moreover, UCOs faithfully recapitulated early corticogenesis, concomitant with the establishment of neuroepithelial populations, cortical plate neurons, and glial cells. Furthermore, UCOs systematically developed neural networks and exhibited both excitatory and inhibitory electrophysiological signals when exposed to neurotransmission blockers. Neurodevelopmental disease models derived from UCOs manifested neurite outgrowth defects, which could be ameliorated with targeted drug treatment. We propose UCOs as an advanced platform with low organoid variations and high reproducibility for modeling both brain development and neurological diseases.

摘要

人类大脑类器官是研究大脑发育和神经系统疾病发病机制的有前景的工具。为了将类器官用于药物有效性和安全性筛选,每个孔中接种的类器官必须在与细胞完全相同的条件下制备。尽管在改善类器官生成方法方面进行了数十年的广泛研究,但仍然存在各种挑战,例如产量低以及批次内和批次间大小和分化的异质性。在这里,我们通过优化类器官大小并对端脑分化标志物表达进行实时监测,新建立了源自诱导多能干细胞的均匀大脑类器官(UCO)。这些类器官在端脑分化过程中表现出形态均匀性和一致的表达,且产量高。此外,UCO忠实地重现了早期皮质发生,同时建立了神经上皮群体、皮质板神经元和胶质细胞。此外,UCO系统地发育神经网络,并在暴露于神经传递阻滞剂时表现出兴奋性和抑制性电生理信号。源自UCO的神经发育疾病模型表现出神经突生长缺陷,这可以通过靶向药物治疗得到改善。我们提出UCO作为一个先进的平台,具有低类器官变异性和高重现性,可用于模拟大脑发育和神经系统疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e52/11538552/5eff50d3843d/bmr.0104.fig.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e52/11538552/9eaa72d2c6ea/bmr.0104.fig.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e52/11538552/d391660bf7c3/bmr.0104.fig.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e52/11538552/1c8225a73112/bmr.0104.fig.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e52/11538552/1cb5a4e9be72/bmr.0104.fig.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e52/11538552/5eff50d3843d/bmr.0104.fig.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e52/11538552/9eaa72d2c6ea/bmr.0104.fig.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e52/11538552/d391660bf7c3/bmr.0104.fig.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e52/11538552/1c8225a73112/bmr.0104.fig.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e52/11538552/1cb5a4e9be72/bmr.0104.fig.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e52/11538552/5eff50d3843d/bmr.0104.fig.005.jpg

相似文献

1
Manufacturing Uniform Cerebral Organoids for Neurological Disease Modeling and Drug Evaluation.制造用于神经疾病建模和药物评估的均匀脑类器官
Biomater Res. 2024 Nov 6;28:0104. doi: 10.34133/bmr.0104. eCollection 2024.
2
Dynamic Characterization of Structural, Molecular, and Electrophysiological Phenotypes of Human-Induced Pluripotent Stem Cell-Derived Cerebral Organoids, and Comparison with Fetal and Adult Gene Profiles.人诱导多能干细胞衍生脑类器官的结构、分子和电生理表型的动态特征,并与胎儿和成人基因谱进行比较。
Cells. 2020 May 23;9(5):1301. doi: 10.3390/cells9051301.
3
A Hybrid 2D-to-3D in vitro Differentiation Platform Improves Outcomes of Cerebral Cortical Organoid Generation in hiPSCs.一种混合的 2D 到 3D 体外分化平台可提高 hiPSC 来源的大脑皮质类器官生成的效率。
Curr Protoc. 2024 Oct;4(10):e70022. doi: 10.1002/cpz1.70022.
4
Human brain organoid-on-a-chip to model prenatal nicotine exposure.类脑器官芯片模型研究产前尼古丁暴露
Lab Chip. 2018 Mar 13;18(6):851-860. doi: 10.1039/c7lc01084b.
5
Production of Phenotypically Uniform Human Cerebral Organoids from Pluripotent Stem Cells.从多能干细胞生成表型一致的人类大脑类器官。
Bio Protoc. 2021 Apr 20;11(8):e3985. doi: 10.21769/BioProtoc.3985.
6
A Simple Method for Generating Cerebral Organoids from Human Pluripotent Stem Cells.一种从人多能干细胞生成脑类器官的简单方法。
Int J Stem Cells. 2022 Feb 28;15(1):95-103. doi: 10.15283/ijsc21195.
7
Human Cytomegalovirus Compromises Development of Cerebral Organoids.人类巨细胞病毒损害脑类器官的发育。
J Virol. 2019 Aug 13;93(17). doi: 10.1128/JVI.00957-19. Print 2019 Sep 1.
8
Establishment of human cerebral organoid systems to model early neural development and assess the central neurotoxicity of environmental toxins.建立人类大脑类器官系统以模拟早期神经发育并评估环境毒素的中枢神经毒性。
Neural Regen Res. 2025 Jan 1;20(1):242-252. doi: 10.4103/NRR.NRR-D-23-00928. Epub 2024 Jan 31.
9
Novel model of cortical-meningeal organoid co-culture system improves human cortical brain organoid cytoarchitecture.新型皮质脑膜器官共培养模型改善了人类皮质脑类器官的细胞结构。
Sci Rep. 2023 May 14;13(1):7809. doi: 10.1038/s41598-023-35077-9.
10
Uniform cerebral organoid culture on a pillar plate by simple and reproducible spheroid transfer from an ultralow attachment well plate.通过简单且可重复的从超低附着培养板转移到柱状培养板来实现脑类器官的均匀培养。
Biofabrication. 2024 Jan 16;16(2). doi: 10.1088/1758-5090/ad1b1e.

引用本文的文献

1
Hydrogen Peroxide-Releasing Hydrogel-Mediated Cellular Senescence Model for Aging Research.用于衰老研究的过氧化氢释放水凝胶介导的细胞衰老模型
Biomater Res. 2025 Mar 14;29:0161. doi: 10.34133/bmr.0161. eCollection 2025.
2
Toxicity assessment using neural organoids: innovative approaches and challenges.使用神经类器官进行毒性评估:创新方法与挑战
Toxicol Res. 2025 Feb 12;41(2):91-103. doi: 10.1007/s43188-025-00279-y. eCollection 2025 Mar.
3
Brain organoid methodologies to explore mechanisms of disease in progressive multiple sclerosis.

本文引用的文献

1
Complex heatmap visualization.复杂热图可视化。
Imeta. 2022 Aug 1;1(3):e43. doi: 10.1002/imt2.43. eCollection 2022 Sep.
2
Trofinetide in Rett syndrome: A brief review of safety and efficacy.曲非奈肽治疗瑞特综合征:安全性与疗效简要综述
Intractable Rare Dis Res. 2023 Nov;12(4):262-266. doi: 10.5582/irdr.2023.01060.
3
MeCP2 dysfunction prevents proper BMP signaling and neural progenitor expansion in brain organoid.MeCP2 功能障碍可阻止脑类器官中 BMP 信号的正常传递和神经祖细胞的扩增。
用于探索进展性多发性硬化症疾病机制的脑类器官方法
Front Cell Neurosci. 2024 Dec 18;18:1488691. doi: 10.3389/fncel.2024.1488691. eCollection 2024.
Ann Clin Transl Neurol. 2023 Jul;10(7):1170-1185. doi: 10.1002/acn3.51799. Epub 2023 Jun 11.
4
Human pluripotent-stem-cell-derived organoids for drug discovery and evaluation.人多能干细胞衍生类器官用于药物发现和评价。
Cell Stem Cell. 2023 May 4;30(5):571-591. doi: 10.1016/j.stem.2023.04.011.
5
Trofinetide Receives FDA Approval as First Drug for Rett Syndrome.曲非奈肽获美国食品药品监督管理局批准,成为首个用于治疗雷特综合征的药物。
JAMA. 2023 Apr 11;329(14):1142. doi: 10.1001/jama.2023.4003.
6
Functional neuronal circuitry and oscillatory dynamics in human brain organoids.人类脑类器官中的功能性神经元回路和振荡动力学。
Nat Commun. 2022 Jul 29;13(1):4403. doi: 10.1038/s41467-022-32115-4.
7
Enhanced cortical neural stem cell identity through short SMAD and WNT inhibition in human cerebral organoids facilitates emergence of outer radial glial cells.通过在人神经脑器官中短暂抑制 SMAD 和 WNT 增强皮质神经干细胞特性,有利于外放射状胶质细胞的出现。
Nat Cell Biol. 2022 Jun;24(6):981-995. doi: 10.1038/s41556-022-00929-5. Epub 2022 Jun 13.
8
The Role of the Extracellular Matrix in Neural Progenitor Cell Proliferation and Cortical Folding During Human Neocortex Development.细胞外基质在人类新皮层发育过程中神经祖细胞增殖和皮质折叠中的作用
Front Cell Neurosci. 2022 Jan 24;15:804649. doi: 10.3389/fncel.2021.804649. eCollection 2021.
9
Modeling human neurodevelopmental diseases with brain organoids.利用脑类器官模拟人类神经发育疾病。
Cell Regen. 2022 Jan 4;11(1):1. doi: 10.1186/s13619-021-00103-6.
10
Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases.神经原兴奋-抑制平衡在遗传神经疾病的类器官模型中被改变。
Mol Brain. 2021 Oct 11;14(1):156. doi: 10.1186/s13041-021-00864-w.