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诱导多能干细胞(iPSCs):诱导的分子机制与应用。

Induced pluripotent stem cells (iPSCs): molecular mechanisms of induction and applications.

机构信息

Department of Neurodegenerative Diseases, Beckman Research Institute of City of Hope, Duarte, CA, 91010, USA.

Irell & Manella Graduate School of Biological Sciences, Beckman Research Institute of City of Hope, Duarte, CA, 91010, USA.

出版信息

Signal Transduct Target Ther. 2024 Apr 26;9(1):112. doi: 10.1038/s41392-024-01809-0.


DOI:10.1038/s41392-024-01809-0
PMID:38670977
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11053163/
Abstract

The induced pluripotent stem cell (iPSC) technology has transformed in vitro research and holds great promise to advance regenerative medicine. iPSCs have the capacity for an almost unlimited expansion, are amenable to genetic engineering, and can be differentiated into most somatic cell types. iPSCs have been widely applied to model human development and diseases, perform drug screening, and develop cell therapies. In this review, we outline key developments in the iPSC field and highlight the immense versatility of the iPSC technology for in vitro modeling and therapeutic applications. We begin by discussing the pivotal discoveries that revealed the potential of a somatic cell nucleus for reprogramming and led to successful generation of iPSCs. We consider the molecular mechanisms and dynamics of somatic cell reprogramming as well as the numerous methods available to induce pluripotency. Subsequently, we discuss various iPSC-based cellular models, from mono-cultures of a single cell type to complex three-dimensional organoids, and how these models can be applied to elucidate the mechanisms of human development and diseases. We use examples of neurological disorders, coronavirus disease 2019 (COVID-19), and cancer to highlight the diversity of disease-specific phenotypes that can be modeled using iPSC-derived cells. We also consider how iPSC-derived cellular models can be used in high-throughput drug screening and drug toxicity studies. Finally, we discuss the process of developing autologous and allogeneic iPSC-based cell therapies and their potential to alleviate human diseases.

摘要

诱导多能干细胞(iPSC)技术改变了体外研究,为推进再生医学带来了巨大的希望。iPSC 具有几乎无限扩增的能力,易于基因工程操作,并且可以分化为大多数体细胞类型。iPSC 已广泛应用于人类发育和疾病建模、药物筛选和细胞治疗的开发。在这篇综述中,我们概述了 iPSC 领域的关键进展,并强调了 iPSC 技术在体外建模和治疗应用中的巨大多功能性。我们首先讨论了揭示体细胞核重编程潜力并成功产生 iPSC 的关键发现。我们考虑体细胞重编程的分子机制和动力学,以及诱导多能性的多种方法。随后,我们讨论了各种基于 iPSC 的细胞模型,从单一细胞类型的单核培养物到复杂的三维类器官,以及这些模型如何应用于阐明人类发育和疾病的机制。我们使用神经退行性疾病、2019 年冠状病毒病(COVID-19)和癌症的例子来说明可以使用 iPSC 衍生细胞建模的多种疾病特异性表型。我们还考虑了如何使用 iPSC 衍生的细胞模型进行高通量药物筛选和药物毒性研究。最后,我们讨论了开发自体和同种异体 iPSC 为基础的细胞治疗的过程及其缓解人类疾病的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cbd/11053163/c4a0aad91e04/41392_2024_1809_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cbd/11053163/ec49e020523d/41392_2024_1809_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cbd/11053163/bb141d78ffa8/41392_2024_1809_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cbd/11053163/f328c1fbabe0/41392_2024_1809_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cbd/11053163/f385c128b22c/41392_2024_1809_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cbd/11053163/aac7eae97fb0/41392_2024_1809_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cbd/11053163/527cd0ef14ca/41392_2024_1809_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cbd/11053163/c4a0aad91e04/41392_2024_1809_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cbd/11053163/ec49e020523d/41392_2024_1809_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cbd/11053163/bb141d78ffa8/41392_2024_1809_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cbd/11053163/f328c1fbabe0/41392_2024_1809_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cbd/11053163/f385c128b22c/41392_2024_1809_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cbd/11053163/aac7eae97fb0/41392_2024_1809_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cbd/11053163/527cd0ef14ca/41392_2024_1809_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cbd/11053163/c4a0aad91e04/41392_2024_1809_Fig7_HTML.jpg

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本文引用的文献

[1]
PTCH1-mutant human cerebellar organoids exhibit altered neural development and recapitulate early medulloblastoma tumorigenesis.

Dis Model Mech. 2024-2-1

[2]
Thalamocortical organoids enable in vitro modeling of 22q11.2 microdeletion associated with neuropsychiatric disorders.

Cell Stem Cell. 2024-3-7

[3]
Derivation of human primordial germ cell-like cells in an embryonic-like culture.

Nat Commun. 2024-1-2

[4]
The rise of epitranscriptomics: recent developments and future directions.

Trends Pharmacol Sci. 2024-1

[5]
The evolution of embryo models.

Nat Methods. 2023-12

[6]
Myelin organoids for the study of Alzheimer's disease.

Front Neurosci. 2023-10-24

[7]
Developing a human iPSC-derived three-dimensional myelin spheroid platform for modeling myelin diseases.

iScience. 2023-9-25

[8]
Live-cell three-dimensional single-molecule tracking reveals modulation of enhancer dynamics by NuRD.

Nat Struct Mol Biol. 2023-11

[9]
Generating hematopoietic cells from human pluripotent stem cells: approaches, progress and challenges.

Cell Regen. 2023-9-1

[10]
Astrocytic response mediated by the CLU risk allele inhibits OPC proliferation and myelination in a human iPSC model.

Cell Rep. 2023-8-29

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