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使用小分子而非外源性转录因子进行重编程。

Reprogramming with Small Molecules instead of Exogenous Transcription Factors.

作者信息

Lin Tongxiang, Wu Shouhai

机构信息

Guangzhou University of Chinese Medicine, The Second Affiliated Hospital (Guangdong Provincial Hospital of Chinese Medicine), 55 Neihuan W. Road, Higher Education Mega Center, Guangzhou, Guangdong 510006, China ; Fujian Agriculture and Forestry University, Stem Cell Research Center, 15 Shangxiadian Road, Cangshan District, Fuzhou, Fujian 350002, China.

Guangzhou University of Chinese Medicine, The Second Affiliated Hospital (Guangdong Provincial Hospital of Chinese Medicine), 55 Neihuan W. Road, Higher Education Mega Center, Guangzhou, Guangdong 510006, China.

出版信息

Stem Cells Int. 2015;2015:794632. doi: 10.1155/2015/794632. Epub 2015 Apr 1.

DOI:10.1155/2015/794632
PMID:25922608
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4397468/
Abstract

Induced pluripotent stem cells (iPSCs) could be employed in the creation of patient-specific stem cells, which could subsequently be used in various basic and clinical applications. However, current iPSC methodologies present significant hidden risks with respect to genetic mutations and abnormal expression which are a barrier in realizing the full potential of iPSCs. A chemical approach is thought to be a promising strategy for safety and efficiency of iPSC generation. Many small molecules have been identified that can be used in place of exogenous transcription factors and significantly improve iPSC reprogramming efficiency and quality. Recent studies have shown that the use of small molecules results in the generation of chemically induced pluripotent stem cells from mouse embryonic fibroblast cells. These studies might lead to new areas of stem cell research and medical applications, not only human iPSC by chemicals alone, but also safe generation of somatic stem cells for cell based clinical trials and other researches. In this paper, we have reviewed the recent advances in small molecule approaches for the generation of iPSCs.

摘要

诱导多能干细胞(iPSC)可用于创建患者特异性干细胞,随后可用于各种基础和临床应用。然而,目前的iPSC方法在基因突变和异常表达方面存在重大潜在风险,这是实现iPSC全部潜力的一个障碍。化学方法被认为是一种有前景的iPSC生成策略,有望提高其安全性和效率。许多小分子已被确定可用于替代外源性转录因子,并显著提高iPSC重编程效率和质量。最近的研究表明,使用小分子可从小鼠胚胎成纤维细胞生成化学诱导多能干细胞。这些研究可能会开辟干细胞研究和医学应用的新领域,不仅包括仅通过化学方法生成人类iPSC,还包括安全生成用于基于细胞的临床试验和其他研究的体细胞干细胞。在本文中,我们综述了小分子方法在iPSC生成方面的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba8d/4397468/f53ddebb6cd9/SCI2015-794632.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba8d/4397468/e9740b5a3c5b/SCI2015-794632.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba8d/4397468/631941fad7c8/SCI2015-794632.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba8d/4397468/f53ddebb6cd9/SCI2015-794632.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba8d/4397468/e9740b5a3c5b/SCI2015-794632.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba8d/4397468/631941fad7c8/SCI2015-794632.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba8d/4397468/f53ddebb6cd9/SCI2015-794632.003.jpg

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