Department of Cell Biology and Human Anatomy, Institute for Pediatric Regenerative Medicine, School of Medicine, University of California, Davis, CA, USA.
Bioessays. 2010 May;32(5):385-7. doi: 10.1002/bies.201000014.
Current methods of reprogramming differentiated cells into induced pluripotent stem cells remain slow and inefficient. In a recent report published online in Nature, Bhutani et al.1 developed a cell fusion strategy, achieving quick and efficient reprogramming toward pluripotency. Using this assay, they identified an immune system protein called activation-induced cytidine deaminase, or AID, which unexpectedly is actually able to "aid" in reprogramming due to its involvement in DNA demethylation that is required for induction of the two key pluripotency genes, Oct4 and Nanog. More recently, Popp et al. 2 also reported online in Nature that AID is important for complete cell reprogramming in mammals. Together, these findings provide new insights into how cells are reprogrammed, identify the specific role of AID in cell fate reversal, and advance the field of regenerative medicine.
目前将分化细胞重编程为诱导多能干细胞的方法仍然很慢且效率低下。在最近发表在《自然》杂志上的一项研究中,Bhutani 等人 1 开发了一种细胞融合策略,实现了快速高效的多能性重编程。他们使用这种检测方法鉴定了一种称为激活诱导胞嘧啶脱氨酶(activation-induced cytidine deaminase,AID)的免疫系统蛋白,出乎意料的是,由于 AID 参与了诱导两个关键多能性基因 Oct4 和 Nanog 所需的 DNA 去甲基化,它实际上能够“辅助”重编程。最近,Popp 等人 2 也在《自然》杂志上在线报道称,AID 对于哺乳动物的完全细胞重编程很重要。总之,这些发现为细胞如何被重编程提供了新的见解,确定了 AID 在细胞命运逆转中的特定作用,并推进了再生医学领域。