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用于临床应用的诱导多能干细胞衍生类器官的优点与挑战。

Merits and challenges of iPSC-derived organoids for clinical applications.

作者信息

Xu Ziran, Yang Jiaxu, Xin Xianyi, Liu Chengrun, Li Lisha, Mei Xianglin, Li Meiying

机构信息

The Key Laboratory of Pathobiology, Ministry of Education, Jilin University, Changchun, Jilin, China.

Department of Clinical Laboratory, Lequn Branch, The First Hospital of Jilin University, Changchun, Jilin, China.

出版信息

Front Cell Dev Biol. 2023 May 26;11:1188905. doi: 10.3389/fcell.2023.1188905. eCollection 2023.

DOI:10.3389/fcell.2023.1188905
PMID:37305682
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10250752/
Abstract

Induced pluripotent stem cells (iPSCs) have entered an unprecedented state of development since they were first generated. They have played a critical role in disease modeling, drug discovery, and cell replacement therapy, and have contributed to the evolution of disciplines such as cell biology, pathophysiology of diseases, and regenerative medicine. Organoids, the stem cell-derived 3D culture systems that mimic the structure and function of organs , have been widely used in developmental research, disease modeling, and drug screening. Recent advances in combining iPSCs with 3D organoids are facilitating further applications of iPSCs in disease research. Organoids derived from embryonic stem cells, iPSCs, and multi-tissue stem/progenitor cells can replicate the processes of developmental differentiation, homeostatic self-renewal, and regeneration due to tissue damage, offering the potential to unravel the regulatory mechanisms of development and regeneration, and elucidate the pathophysiological processes involved in disease mechanisms. Herein, we have summarized the latest research on the production scheme of organ-specific iPSC-derived organoids, the contribution of these organoids in the treatment of various organ-related diseases, in particular their contribution to COVID-19 treatment, and have discussed the unresolved challenges and shortcomings of these models.

摘要

诱导多能干细胞(iPSC)自首次产生以来,已进入了前所未有的发展阶段。它们在疾病建模、药物发现和细胞替代疗法中发挥了关键作用,并推动了细胞生物学、疾病病理生理学和再生医学等学科的发展。类器官是一种源自干细胞的三维培养系统,可模拟器官的结构和功能,已广泛应用于发育研究、疾病建模和药物筛选。将iPSC与三维类器官相结合的最新进展,正在推动iPSC在疾病研究中的进一步应用。源自胚胎干细胞、iPSC和多组织干细胞/祖细胞的类器官,能够复制发育分化、稳态自我更新以及因组织损伤而再生的过程,这为揭示发育和再生的调控机制以及阐明疾病机制中涉及的病理生理过程提供了潜力。在此,我们总结了关于器官特异性iPSC衍生类器官生产方案的最新研究、这些类器官在治疗各种器官相关疾病中的作用,特别是它们对COVID-19治疗的贡献,并讨论了这些模型尚未解决的挑战和不足之处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/285b/10250752/1d8025c608e9/fcell-11-1188905-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/285b/10250752/9ab998ca1eba/fcell-11-1188905-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/285b/10250752/b8bd803f7061/fcell-11-1188905-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/285b/10250752/e615490b3473/fcell-11-1188905-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/285b/10250752/1d8025c608e9/fcell-11-1188905-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/285b/10250752/9ab998ca1eba/fcell-11-1188905-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/285b/10250752/b8bd803f7061/fcell-11-1188905-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/285b/10250752/e615490b3473/fcell-11-1188905-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/285b/10250752/1d8025c608e9/fcell-11-1188905-g004.jpg

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2
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PLoS Biol. 2022 Nov 3;20(11):e3001845. doi: 10.1371/journal.pbio.3001845. eCollection 2022 Nov.
3
Human Nasal Organoids Model SARS-CoV-2 Upper Respiratory Infection and Recapitulate the Differential Infectivity of Emerging Variants.
Small Sci. 2024 Sep 19;4(11):2400314. doi: 10.1002/smsc.202400314. eCollection 2024 Nov.
4
An update on mammalian and non-mammalian animal models for biomarker development in neurodegenerative disorders.神经退行性疾病生物标志物开发的哺乳动物和非哺乳动物动物模型的最新进展。
Cell Mol Life Sci. 2025 Apr 7;82(1):147. doi: 10.1007/s00018-025-05668-y.
5
Advances in humanoid organoid-based research on inter-organ communications during cardiac organogenesis and cardiovascular diseases.基于类器官的人体心脏器官发生和心血管疾病期间器官间通讯研究进展。
J Transl Med. 2025 Mar 28;23(1):380. doi: 10.1186/s12967-025-06381-x.
6
Induced pluripotent stem cell-related approaches to generate dopaminergic neurons for Parkinson's disease.用于帕金森病的诱导多能干细胞相关方法来生成多巴胺能神经元。
Neural Regen Res. 2025 Nov 1;20(11):3193-3206. doi: 10.4103/NRR.NRR-D-24-00771. Epub 2024 Dec 7.
7
A comprehensive review of electrophysiological techniques in amyotrophic lateral sclerosis research.肌萎缩侧索硬化症研究中电生理技术的全面综述。
Front Cell Neurosci. 2024 Aug 30;18:1435619. doi: 10.3389/fncel.2024.1435619. eCollection 2024.
8
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Adv Sci (Weinh). 2024 Aug;11(32):e2403892. doi: 10.1002/advs.202403892. Epub 2024 Jun 23.
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Induced Pluripotent Stem Cells and CRISPR-Cas9 Innovations for Treating Alpha-1 Antitrypsin Deficiency and Glycogen Storage Diseases.诱导多能干细胞和 CRISPR-Cas9 创新技术治疗 α-1 抗胰蛋白酶缺乏症和糖原贮积病。
Cells. 2024 Jun 18;13(12):1052. doi: 10.3390/cells13121052.
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