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探索类器官和组装体技术:聚焦于视网膜和大脑。

Exploring organoid and assembloid technologies: a focus on retina and brain.

作者信息

Ouaidat Sara, Bellapianta Alessandro, Ammer-Pickhardt Franziska, Taghipour Tara, Bolz Matthias, Salti Ahmad

机构信息

Research Group Cellular and Molecular Ophthalmology, University Clinic for Ophthalmology and Optometry, Kepler University Hospital, Johannes Kepler University Linz, Linz, Austria.

Department of Biosciences & Medical Biology, Paris-Lodron-University of Salzburg (PLUS), Salzburg, Austria.

出版信息

Expert Rev Mol Med. 2025 Mar 27;27:e14. doi: 10.1017/erm.2025.9.

DOI:10.1017/erm.2025.9
PMID:40145178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12011387/
Abstract

BACKGROUND

The recent emergence of three-dimensional organoids and their utilization as in vitro disease models confirmed the complexities behind organ-specific functions and unravelled the importance of establishing suitable human models for various applications. Also, in light of persistent challenges associated with their use, researchers have been striving to establish more advanced structures (i.e. assembloids) that can help address the limitations presented in the current organoids.

METHODS

In this review, we discuss the distinct organoid types that are available to date, with a special focus on retinal and brain organoids, and highlight their importance in disease modelling.

RESULTS

We refer to published research to explore the extent to which retinal and brain organoids can serve as potential alternatives to organ/cell transplants and direct our attention to the topic of photostimulation in retinal organoids. Additionally, we discuss the advantages of incorporating microfluidics and organ-on-a-chip devices for boosting retinal organoid performance. The challenges of organoids leading to the subsequent development of assembloid fusion models are also presented.

CONCLUSION

In conclusion, organoid technology has laid the foundation for generating upgraded models that not only better replicate in vivo systems but also allow for a deeper comprehension of disease pathophysiology.

摘要

背景

三维类器官的近期出现及其作为体外疾病模型的应用,证实了器官特异性功能背后的复杂性,并揭示了建立适用于各种应用的人体模型的重要性。此外,鉴于其使用中存在的持续挑战,研究人员一直在努力建立更先进的结构(即组装体),以帮助解决当前类器官中存在的局限性。

方法

在本综述中,我们讨论了迄今为止可用的不同类型的类器官,特别关注视网膜和脑类器官,并强调它们在疾病建模中的重要性。

结果

我们参考已发表的研究,探讨视网膜和脑类器官可在多大程度上作为器官/细胞移植的潜在替代物,并将我们的注意力引向视网膜类器官中的光刺激主题。此外,我们讨论了结合微流体和芯片器官装置以提高视网膜类器官性能的优势。还介绍了类器官导致组装体融合模型后续发展的挑战。

结论

总之,类器官技术为生成升级模型奠定了基础,这些模型不仅能更好地复制体内系统,还能更深入地理解疾病病理生理学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a90/12011387/2e8cd8b1d432/S1462399425000092_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a90/12011387/7b2a873b7e76/S1462399425000092_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a90/12011387/98d570bd7fed/S1462399425000092_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a90/12011387/2e8cd8b1d432/S1462399425000092_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a90/12011387/7b2a873b7e76/S1462399425000092_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a90/12011387/98d570bd7fed/S1462399425000092_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a90/12011387/2e8cd8b1d432/S1462399425000092_fig3.jpg

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本文引用的文献

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Non-Invasive Quality Control of Organoid Cultures Using Mesofluidic CSTR Bioreactors and High-Content Imaging.使用微流控连续搅拌槽式生物反应器和高内涵成像技术对类器官培养物进行非侵入性质量控制
Adv Mater Technol. 2025 Feb 5;10(3). doi: 10.1002/admt.202400473. Epub 2024 Aug 31.
2
Human assembloid model of the ascending neural sensory pathway.上行神经感觉通路的人类类组装体模型。
Nature. 2025 Apr 9. doi: 10.1038/s41586-025-08808-3.
3
Model construction and clinical therapeutic potential of engineered cardiac organoids for cardiovascular diseases.
用于心血管疾病的工程化心脏类器官的模型构建及临床治疗潜力
Biomater Transl. 2024 Nov 15;5(4):337-354. doi: 10.12336/biomatertransl.2024.04.002. eCollection 2024.
4
Advances in liver organoids: replicating hepatic complexity for toxicity assessment and disease modeling.肝脏类器官的进展:复制肝脏复杂性用于毒性评估和疾病建模。
Stem Cell Res Ther. 2025 Jan 26;16(1):27. doi: 10.1186/s13287-025-04139-2.
5
Advances in cardiac organoid research: implications for cardiovascular disease treatment.心脏类器官研究进展:对心血管疾病治疗的意义
Cardiovasc Diabetol. 2025 Jan 18;24(1):25. doi: 10.1186/s12933-025-02598-8.
6
Transplantation of genome-edited retinal organoids restores some fundamental physiological functions coordinated with severely degenerated host retinas.基因组编辑的视网膜类器官移植可恢复一些与严重退化的宿主视网膜协调的基本生理功能。
Stem Cell Reports. 2025 Feb 11;20(2):102393. doi: 10.1016/j.stemcr.2024.102393. Epub 2025 Jan 16.
7
Intestinal organoids: The path towards clinical application.肠道类器官:通往临床应用之路。
Eur J Cell Biol. 2025 Mar;104(1):151474. doi: 10.1016/j.ejcb.2024.151474. Epub 2024 Dec 25.
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Harnessing 3D models to uncover the mechanisms driving infectious and inflammatory disease in the intestine.利用三维模型揭示肠道感染性和炎症性疾病的发病机制。
BMC Biol. 2024 Dec 31;22(1):300. doi: 10.1186/s12915-024-02092-9.
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