Center for Regenerative Medicine Barcelona, Barcelona, Spain.
Cell Cycle. 2010 Oct 1;9(19):3887-91. doi: 10.4161/cc.9.19.13301. Epub 2010 Oct 9.
The reprogramming of somatic cells to induced pluripotent stem (iPS) cells is one of the major discoveries of recent years. The development and application of patient specific iPS lines could potentially revolutionise cell-based therapy, facilitating the treatment of a wide range of diseases. Despite the numerous technological advancements in the field, an in-depth mechanistical understanding of the pathways involved in reprogramming is still lacking. Several groups have recently provided a mechanistical insight into the role of the p53 tumour suppressor pathway in reprogramming. The repercussions of these findings are profound and reveal an unexpected role of p53 as a "guardian of reprogramming", ensuring genomic integrity during reprogramming at the cost of a reduced efficiency of the process. Here we analyse the latest findings in the field and discuss their relevance for future applications of iPS cell technology.
体细胞重编程为诱导多能干细胞(iPS 细胞)是近年来的重大发现之一。患者特异性 iPS 系的开发和应用可能会彻底改变基于细胞的治疗,为广泛的疾病治疗带来便利。尽管该领域取得了众多技术进步,但对重编程所涉及的途径的深入机制理解仍有所欠缺。最近,有几个研究小组深入了解了 p53 肿瘤抑制途径在重编程中的作用。这些发现意义深远,揭示了 p53 出人意料的作用,即作为“重编程的守护者”,在重编程过程中确保基因组完整性,代价是降低了该过程的效率。本文我们分析了该领域的最新发现,并讨论了它们对未来 iPS 细胞技术应用的相关性。