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Transactivator protein:An alternative for delivery of recombinant proteins for safer reprogramming of induced Pluripotent Stem Cell

机译:反式激活蛋白:传递重组蛋白的一种替代方法,可以更安全地重编程诱导的多能干细胞

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摘要

Induced pluripotent stem cells (iPSC) are somatic cells reprogrammed to pluripotency by forced expression of pluripotency factors. These cells are shown to have the same pluripotent potential as embryonic stem cells (ESC) and considered as an alternative to the much controversial usage of ESC which involved human embryos. However, the traditional method in reprogramming cells into iPSC using genome-integrating retro- or lenti- viruses remains an obstacle for its application in clinical setting. Although numerous studies have been conducted for a safer DNA-based reprogramming, reprogramming of iPSC by genetic modifications may raise the possibility of malignant transformation and has been a major limitation for its usage in clinical applications. Therefore, there is a need for an alternative method to reprogram the cells without the use of gene editing and a much safer way to deliver transcription factors to induce pluripotency on target cells. Using protein transduction approach, a number of studies have demonstrated the generation of human iPSCs from human fibroblasts and mouse embryonic fibroblasts by direct delivery of reprogramming proteins. In this review, the definition and mechanism of HIV-TAT protein (a type of protein transduction domain) in delivering recombinant proteins, including the potential of protein-based delivery to induce iPSC were further discussed.
机译:诱导多能干细胞(iPSC)是通过强制表达多能性因子而重新编程为多能性的体细胞。这些细胞具有与胚胎干细胞(ESC)相同的多能潜能,并被认为是涉及人类胚胎的ESC备受争议的替代方法。但是,使用整合基因组的逆转录病毒或慢病毒将细胞重编程为iPSC的传统方法仍然是其在临床中应用的障碍。尽管已进行了许多研究,以更安全地进行基于DNA的重编程,但通过基因修饰对iPSC进行重编程可能会增加恶性转化的可能性,并且已成为其在临床应用中的主要限制。因此,需要在不使用基因编辑的情况下重新编程细胞的替代方法以及递送转录因子以在靶细胞上诱导多能性的更安全的方法。使用蛋白质转导方法,许多研究已证明通过直接递送重编程蛋白质可从人成纤维细胞和小鼠胚胎成纤维细胞中生成人iPSC。在这篇综述中,进一步讨论了HIV-TAT蛋白(一种蛋白转导域)在传递重组蛋白中的定义和机理,包括基于蛋白的传递诱导iPSC的潜力。

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