Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8917281 | Science Bulletin | 2018 | 25 Pages |
Abstract
Embryonic stem cells (ESCs) maintain their cellular identity through the systematic regulation of master transcription factors and chromatin remodeling complexes. Recent work has shown that the unusually large-scale enhancers-namely super-enhancers (SEs), on which BRD4, a member of the bromodomain and extraterminal domain (BET) family is highly enriched-could regulate pluripotency-related transcription factors. Moreover, inhibition of BRD4 binding on SEs has been shown to induce the differentiation of ESCs. However, the underlying mechanism of BRD4 inhibition-mediated stem cell differentiation remains elusive. Here we show that both mouse and human ESCs lose their capacity for self-renewal upon treatment with JQ1, a selective inhibitor of BET family including BRD4, with rapid suppression of pluripotency-associated genes. Notably, a high concentration of JQ1 could selectively eliminate ESCs via apoptosis, without affecting the functionality of differentiated somatic cells from ESCs, suggesting that inhibition of BET may have a beneficial effect on the development of pluripotent stem cell-based cell therapy.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Chemistry (General)
Authors
Jung Hyun Im, Seon In Hwang, Jong-Wan Kim, Soon-Jung Park, Kyu-ree Kang, Jueng Soo You, Kee Pyo Kim, Sung-Hwan Moon, Hyuk-Jin Cha, Hyung-Min Chung, Hans R. Schöler, Jung Keun Hyun, Dong Wook Han,