| Literature DB >> 26686652 |
Yang Zhao1, Ting Zhao2, Jingyang Guan3, Xu Zhang3, Yao Fu3, Junqing Ye4, Jialiang Zhu3, Gaofan Meng4, Jian Ge3, Susu Yang3, Lin Cheng3, Yaqin Du3, Chaoran Zhao3, Ting Wang3, Linlin Su3, Weifeng Yang5, Hongkui Deng6.
Abstract
Somatic cells can be reprogrammed into pluripotent stem cells (PSCs) by using pure chemicals, providing a different paradigm to study somatic reprogramming. However, the cell fate dynamics and molecular events that occur during the chemical reprogramming process remain unclear. We now show that the chemical reprogramming process requires the early formation of extra-embryonic endoderm (XEN)-like cells and a late transition from XEN-like cells to chemically-induced (Ci)PSCs, a unique route that fundamentally differs from the pathway of transcription factor-induced reprogramming. Moreover, precise manipulation of the cell fate transition in a step-wise manner through the XEN-like state allows us to identify small-molecule boosters and establish a robust chemical reprogramming system with a yield up to 1,000-fold greater than that of the previously reported protocol. These findings demonstrate that chemical reprogramming is a promising approach to manipulate cell fates.Mesh:
Year: 2015 PMID: 26686652 DOI: 10.1016/j.cell.2015.11.017
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582