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タイトル: ZEB2 and MEIS1 independently contribute to hematopoiesis via early hematopoietic enhancer activation
著者: Kitagawa, Yohko
Ikenaka, Akihiro
Sugimura, Ryohichi
Niwa, Akira
Saito, Megumu K.
著者名の別形: 北川, 瑶子
池中, 亮裕
杉村, 竜一
丹羽, 明
齋藤, 潤
キーワード: Natural sciences
Biological sciences
Developmental biology
発行日: 20-Oct-2023
出版者: Elsevier BV
誌名: iScience
巻: 26
号: 10
論文番号: 107893
抄録: Cell differentiation is achieved by acquiring a cell type-specific transcriptional program and epigenetic landscape. While the cell type-specific patterning of enhancers has been shown to precede cell fate decisions, it remains unclear how regulators of these enhancers are induced to initiate cell specification and how they appropriately restrict cells that differentiate. Here, using embryonic stem cell–derived hematopoietic cell differentiation cultures, we show the activation of some hematopoietic enhancers during arterialization of hemogenic endothelium, a prerequisite for hematopoiesis. We further reveal that ZEB2, a factor involved in the transcriptional regulation of arterial endothelial cells, and a hematopoietic regulator MEIS1 are independently required for activating these enhancers. Concomitantly, ZEB2 or MEIS1 deficiency impaired hematopoietic cell development. These results suggest that multiple regulators expressed from an earlier developmental stage non-redundantly contribute to the establishment of hematopoietic enhancer landscape, thereby restricting cell differentiation despite the unrestricted expression of these regulators to hematopoietic cells.
記述: 血球細胞分化に必要な新たな因子を同定. 京都大学プレスリリース. 2023-09-29.
Delineating the dynamic transcriptional and epigenetic landscape regulating hematopoiesis. 京都大学プレスリリース. 2023-10-17.
著作権等: © 2023 The Authors.
This is an open access article under the CC BY-NC-ND license.
URI: http://hdl.handle.net/2433/285251
DOI(出版社版): 10.1016/j.isci.2023.107893
PubMed ID: 37771659
関連リンク: https://www.cira.kyoto-u.ac.jp/j/pressrelease/news/230929-100000.html
https://www.cira.kyoto-u.ac.jp/e/pressrelease/news/231017-110000.html
出現コレクション:学術雑誌掲載論文等

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