通过重编程操纵细胞命运:方法与应用。

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Development Pub Date : 2024-10-01 Epub Date: 2024-09-30 DOI:10.1242/dev.203090
Masaki Yagi, Joy E Horng, Konrad Hochedlinger
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引用次数: 0

摘要

细胞的可塑性会随着发育和分化而逐渐减弱,然而这些过程可以通过使用定义的转录因子将体细胞重编程为诱导多能干细胞(iPSCs)而在实验中逆转。过去15年来,重编程技术的进步使研究人员能够利用患者特异性iPSCs研究疾病,从根本上了解细胞身份是如何维持的,利用各种胚胎模型重现胚胎发生的早期阶段,以及逆转培养细胞和动物的衰老过程。在此,我们回顾并比较了目前可用的重编程方法,包括基于转录因子的方法和基于小分子的方法,以获得具有早期胚胎特征的多能细胞。此外,我们还讨论了我们目前对抵制重编程的机制及其在细胞特性维持中的作用的理解。最后,我们回顾了最近利用重编程因子使细胞和组织恢复活力的努力,以及 iPSCs 在研究植入前发育的新型胚胎模型中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Manipulating cell fate through reprogramming: approaches and applications.

Cellular plasticity progressively declines with development and differentiation, yet these processes can be experimentally reversed by reprogramming somatic cells to induced pluripotent stem cells (iPSCs) using defined transcription factors. Advances in reprogramming technology over the past 15 years have enabled researchers to study diseases with patient-specific iPSCs, gain fundamental insights into how cell identity is maintained, recapitulate early stages of embryogenesis using various embryo models, and reverse aspects of aging in cultured cells and animals. Here, we review and compare currently available reprogramming approaches, including transcription factor-based methods and small molecule-based approaches, to derive pluripotent cells characteristic of early embryos. Additionally, we discuss our current understanding of mechanisms that resist reprogramming and their role in cell identity maintenance. Finally, we review recent efforts to rejuvenate cells and tissues with reprogramming factors, as well as the application of iPSCs in deriving novel embryo models to study pre-implantation development.

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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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