Department of Cell Biology, Yale University, New Haven, CT 06520, USA; Yale Stem Cell Center, Yale University, New Haven, CT 06520, USA.
Department of Biomedical Engineering, Yale University, New Haven, CT 06520, USA; Department of Cell Biology, Second Military Medical University, Shanghai 200433, China.
Cell. 2014 Feb 13;156(4):649-62. doi: 10.1016/j.cell.2014.01.020. Epub 2014 Jan 30.
Reprogramming somatic cells to induced pluripotency by Yamanaka factors is usually slow and inefficient and is thought to be a stochastic process. We identified a privileged somatic cell state, from which acquisition of pluripotency could occur in a nonstochastic manner. Subsets of murine hematopoietic progenitors are privileged whose progeny cells predominantly adopt the pluripotent fate with activation of endogenous Oct4 locus after four to five divisions in reprogramming conditions. Privileged cells display an ultrafast cell cycle of ∼8 hr. In fibroblasts, a subpopulation cycling at a similar ultrafast speed is observed after 6 days of factor expression and is increased by p53 knockdown. This ultrafast cycling population accounts for >99% of the bulk reprogramming activity in wild-type or p53 knockdown fibroblasts. Our data demonstrate that the stochastic nature of reprogramming can be overcome in a privileged somatic cell state and suggest that cell-cycle acceleration toward a critical threshold is an important bottleneck for reprogramming. PAPERCLIP:
通过山中因子将体细胞重编程为诱导多能性通常较慢且效率较低,被认为是一种随机过程。我们鉴定了一种特权体细胞状态,从中可以以非随机的方式获得多能性。小鼠造血祖细胞的亚群是特权的,其后代细胞在重编程条件下经过四到五次分裂后,主要通过内源 Oct4 基因座的激活而采用多能性命运。特权细胞显示出超快的细胞周期,约为 8 小时。在成纤维细胞中,在表达因子 6 天后观察到以类似超快速度循环的亚群,并通过 p53 敲低增加。这个超快循环群体占野生型或 p53 敲低成纤维细胞中大部分重编程活性的 >99%。我们的数据表明,重编程的随机性可以在特权体细胞状态下克服,并表明向关键阈值的细胞周期加速是重编程的一个重要瓶颈。