Li Han, Collado Manuel, Villasante Aranzazu, Strati Katerina, Ortega Sagrario, Cañamero Marta, Blasco Maria A, Serrano Manuel
Tumor Suppression Group, Spanish National Cancer Research Centre (CNIO), 3 Melchor Fernandez Almagro Street, Madrid E-28029, Spain.
Nature. 2009 Aug 27;460(7259):1136-9. doi: 10.1038/nature08290. Epub 2009 Aug 9.
The mechanisms involved in the reprogramming of differentiated cells into induced pluripotent stem (iPS) cells by the three transcription factors Oct4 (also known as Pou5f1), Klf4 and Sox2 remain poorly understood. The Ink4/Arf locus comprises the Cdkn2a-Cdkn2b genes encoding three potent tumour suppressors, namely p16(Ink4a), p19(Arf) and p15(Ink4b), which are basally expressed in differentiated cells and upregulated by aberrant mitogenic signals. Here we show that the locus is completely silenced in iPS cells, as well as in embryonic stem (ES) cells, acquiring the epigenetic marks of a bivalent chromatin domain, and retaining the ability to be reactivated after differentiation. Cell culture conditions during reprogramming enhance the expression of the Ink4/Arf locus, further highlighting the importance of silencing the locus to allow proliferation and reprogramming. Indeed, the three factors together repress the Ink4/Arf locus soon after their expression and concomitant with the appearance of the first molecular markers of 'stemness'. This downregulation also occurs in cells carrying the oncoprotein large-T, which functionally inactivates the pathways regulated by the Ink4/Arf locus, thus indicating that the silencing of the locus is intrinsic to reprogramming and not the result of a selective process. Genetic inhibition of the Ink4/Arf locus has a profound positive effect on the efficiency of iPS cell generation, increasing both the kinetics of reprogramming and the number of emerging iPS cell colonies. In murine cells, Arf, rather than Ink4a, is the main barrier to reprogramming by activation of p53 (encoded by Trp53) and p21 (encoded by Cdkn1a); whereas, in human fibroblasts, INK4a is more important than ARF. Furthermore, organismal ageing upregulates the Ink4/Arf locus and, accordingly, reprogramming is less efficient in cells from old organisms, but this defect can be rescued by inhibiting the locus with a short hairpin RNA. All together, we conclude that the silencing of Ink4/Arf locus is rate-limiting for reprogramming, and its transient inhibition may significantly improve the generation of iPS cells.
由转录因子Oct4(也称为Pou5f1)、Klf4和Sox2将分化细胞重编程为诱导多能干细胞(iPS细胞)所涉及的机制仍知之甚少。Ink4/Arf基因座包含Cdkn2a - Cdkn2b基因,这些基因编码三种有效的肿瘤抑制因子,即p16(Ink4a)、p19(Arf)和p15(Ink4b),它们在分化细胞中基础表达,并由异常的促有丝分裂信号上调。在此我们表明,该基因座在iPS细胞以及胚胎干细胞(ES细胞)中完全沉默,获得了双价染色质结构域的表观遗传标记,并保留了分化后重新激活的能力。重编程过程中的细胞培养条件增强了Ink4/Arf基因座的表达,进一步凸显了沉默该基因座以允许增殖和重编程的重要性。事实上,这三种因子在表达后不久并伴随“干性”的首个分子标记出现时,共同抑制了Ink4/Arf基因座。这种下调也发生在携带癌蛋白大T的细胞中,该癌蛋白在功能上使由Ink4/Arf基因座调控的通路失活,因此表明该基因座的沉默是重编程所固有的,而非选择性过程的结果。对Ink4/Arf基因座的基因抑制对iPS细胞生成效率有深远的积极影响,增加了重编程的动力学以及新出现的iPS细胞集落数量。在鼠细胞中,Arf而非Ink4a是通过激活p53(由Trp53编码)和p21(由Cdkn1a编码)进行重编程的主要障碍;而在人成纤维细胞中,INK4a比ARF更重要。此外,机体衰老会上调Ink4/Arf基因座,因此,来自老年机体的细胞重编程效率较低,但通过用短发夹RNA抑制该基因座可以挽救这一缺陷。总之,我们得出结论,Ink4/Arf基因座的沉默是重编程的限速因素,其瞬时抑制可能显著改善iPS细胞生成。