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抑制BET可选择性地消除未分化的多能干细胞。

Inhibition of BET selectively eliminates undifferentiated pluripotent stem cells.

作者信息

Im Jung Hyun, Hwang Seon In, Kim Jong-Wan, Park Soon-Jung, Kang Kyu-Ree, You Jueng Soo, Kim Kee Pyo, Moon Sung-Hwan, Cha Hyuk-Jin, Chung Hyung-Min, Schöler Hans R, Hyun Jung Keun, Han Dong Wook

机构信息

Department of Stem Cell Biology, School of Medicine, Konkuk University, Seoul 05029, Republic of Korea.

Department of Nanobiomedical Science, Dankook University Graduate School, Cheonan 330714, Republic of Korea.

出版信息

Sci Bull (Beijing). 2018 Apr 30;63(8):477-487. doi: 10.1016/j.scib.2018.02.023. Epub 2018 Mar 15.

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.

摘要

胚胎干细胞(ESCs)通过对主转录因子和染色质重塑复合物的系统调控来维持其细胞特性。最近的研究表明,异常大规模的增强子,即超级增强子(SEs),富含溴结构域和额外末端结构域(BET)家族成员BRD4,能够调控多能性相关转录因子。此外,已证明抑制BRD4与SEs的结合可诱导ESCs分化。然而,BRD4抑制介导的干细胞分化的潜在机制仍不清楚。在此我们表明,用JQ1(一种包括BRD4在内的BET家族的选择性抑制剂)处理后,小鼠和人类ESCs均丧失自我更新能力,多能性相关基因迅速受到抑制。值得注意的是,高浓度的JQ1可通过凋亡选择性地消除ESCs,而不影响源自ESCs的分化体细胞的功能,这表明抑制BET可能对基于多能干细胞的细胞治疗的发展具有有益作用。

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