Suppr超能文献

利用小分子改善体细胞诱导多能干细胞的生成。

Using small molecules to improve generation of induced pluripotent stem cells from somatic cells.

作者信息

Desponts Caroline, Ding Sheng

机构信息

Department of Chemistry, The Scripps Research Institute, La Jolla, CA, USA.

出版信息

Methods Mol Biol. 2010;636:207-18. doi: 10.1007/978-1-60761-691-7_13.

Abstract

Induction of pluripotent stem cells from somatic cells by defined factors was shown to be possible only recently, but already several laboratories have made tremendous strive toward improving and understanding the process. Originally, Oct4, Sox2, Klf4, and cMyc were identified as being the combination of genes necessary to induce reprogramming. It was later shown that cMyc was dispensable; however, in its absence the process was less efficient and took a considerably longer period of time to occur. Furthermore, others have shown that the combination of Oct4, Sox2, Nanog, and Lin28 could also induce reprogramming. One major caveat associated with these techniques remains the need for overexpression of several genes using viral systems. Until very recently, most studies were done using integrating viruses such as retroviruses and lentiviruses. This method ensured that the protein of interested would be expressed at a high concentration and for an adequate period of time necessary to induce reprogramming. Up to date, others have now been able to use different nonintegrative method such as adenovirus and plasmid transfection to induce reprogramming. Furthermore, piggyBac transposition was successfully used to induce reprogramming of murine cells. Most importantly, it was recently published that reprogramming can be induced in the absence of virus, with proteins and small molecules. All of the later methods are appealing since they do not require the integration of the virus or plasmid to exert its effect. However, one avenue that would be all the more therapeutically appealing would be to induce reprogramming in the absence of gene overexpression systems, using small molecules to modulate signaling pathways in the somatic cells. A few molecules have already been identified with the ability to either improve the process or replace one or two of the genes deemed necessary for reprogramming. We have screened successfully for compounds that can replace some of these factors, and share the methods developed following these screens.

摘要

体细胞重编程为多能干细胞的技术直到最近才被证明是可行的,但已有多个实验室为改进和深入了解这一过程付出了巨大努力。最初,Oct4、Sox2、Klf4和cMyc被确定为诱导重编程所需的基因组合。后来发现cMyc并非必需;然而,没有cMyc时,重编程过程效率较低,所需时间也长得多。此外,还有研究表明,Oct4、Sox2、Nanog和Lin28的组合也能诱导重编程。这些技术的一个主要问题是,需要使用病毒系统来过量表达多个基因。直到最近,大多数研究都是使用逆转录病毒和慢病毒等整合型病毒进行的。这种方法可确保目的蛋白在诱导重编程所需的足够长的时间内以高浓度表达。目前,已有其他人能够使用腺病毒和质粒转染等不同的非整合方法来诱导重编程。此外,piggyBac转座已成功用于诱导小鼠细胞重编程。最重要的是,最近有报道称,无需病毒,利用蛋白质和小分子就能诱导重编程。所有这些后来的方法都很有吸引力,因为它们不需要整合病毒或质粒来发挥作用。然而,更具治疗吸引力的途径是,在不使用基因过表达系统的情况下,利用小分子调节体细胞中的信号通路来诱导重编程。已经发现了一些能够改善重编程过程或替代一两个被认为是重编程所必需的基因的分子。我们已经成功筛选出了一些能够替代其中某些因子的化合物,并分享在这些筛选之后开发的方法。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验