Lubanska Dorota, Qemo Ingrid, Byrne Megan, Matthews Kaitlyn N, Fifield Bre-Anne, Brown Jillian, da Silva Elizabeth Fidalgo, Porter Lisa A
Department of Biomedical Sciences, University of Windsor, Ontario, Windsor, Ontario, Canada.
Stem Cells. 2021 Dec;39(12):1688-1700. doi: 10.1002/stem.3453. Epub 2021 Sep 17.
Fully differentiated cells can be reprogrammed through ectopic expression of key transcription factors to create induced pluripotent stem cells. These cells share many characteristics of normal embryonic stem cells and have great promise in disease modeling and regenerative medicine. The process of remodeling has its limitations, including a very low efficiency due to the upregulation of many antiproliferative genes, including cyclin dependent kinase inhibitors CDKN1A and CDKN2A, which serve to protect the cell by inducing apoptotic and senescent programs. Our data reveals a unique cell cycle mechanism enabling mouse fibroblasts to repress cyclin dependent kinase inhibitors through the activation of the epigenetic regulator EZH2 by a cyclin-like protein SPY1. This data reveals that the SPY1 protein is required for reprogramming to a pluripotent state and is capable of increasing reprogramming efficiency.
通过关键转录因子的异位表达,可将完全分化的细胞重编程以创建诱导多能干细胞。这些细胞具有许多正常胚胎干细胞的特征,在疾病建模和再生医学方面极具潜力。重编程过程存在局限性,包括由于许多抗增殖基因上调导致效率极低,这些抗增殖基因包括细胞周期蛋白依赖性激酶抑制剂CDKN1A和CDKN2A,它们通过诱导凋亡和衰老程序来保护细胞。我们的数据揭示了一种独特的细胞周期机制,该机制使小鼠成纤维细胞能够通过类细胞周期蛋白SPY1激活表观遗传调节因子EZH2,从而抑制细胞周期蛋白依赖性激酶抑制剂。该数据表明,SPY1蛋白是重编程至多能状态所必需的,并且能够提高重编程效率。