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利用胚胎和诱导多能干细胞衍生的心脏和神经元细胞进行药物发现模型和毒性测试。

Drug discovery models and toxicity testing using embryonic and induced pluripotent stem-cell-derived cardiac and neuronal cells.

机构信息

BioTalentum Ltd., 2100 Gödöllö, Hungary.

出版信息

Stem Cells Int. 2012;2012:379569. doi: 10.1155/2012/379569. Epub 2012 May 8.

Abstract

Development of induced pluripotent stem cells (iPSCs) using forced expression of specific sets of transcription factors has changed the field of stem cell research extensively. Two important limitations for research application of embryonic stem cells (ESCs), namely, ethical and immunological issues, can be circumvented using iPSCs. Since the development of first iPSCs, tremendous effort has been directed to the development of methods to increase the efficiency of the process and to reduce the extent of genomic modifications associated with the reprogramming procedure. The established lineage-specific differentiation protocols developed for ESCs are being applied to iPSCs, as they have great potential in regenerative medicine for cell therapy, disease modeling either for drug development or for fundamental science, and, last but not least, toxicity testing. This paper reviews efforts aimed at practical development of iPSC differentiation to neural/cardiac lineages and further the use of these iPSCs-derived cells for drug development and toxicity testing.

摘要

利用特定转录因子的强制表达来开发诱导多能干细胞(iPSCs)已经广泛改变了干细胞研究领域。使用 iPSCs 可以避免胚胎干细胞(ESCs)研究应用的两个重要限制,即伦理和免疫问题。自第一个 iPSCs 的开发以来,人们已经做出了巨大的努力来开发方法来提高该过程的效率,并减少与重编程过程相关的基因组修饰的程度。已经针对 ESCs 开发了建立的谱系特异性分化方案,并将其应用于 iPSCs,因为它们在再生医学中的细胞治疗、用于药物开发或基础科学的疾病建模以及最后但并非最不重要的毒性测试方面具有巨大的潜力。本文综述了旨在将 iPSC 分化为神经/心脏谱系的实际发展的努力,以及进一步将这些 iPSCs 衍生细胞用于药物开发和毒性测试。

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