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  Lgr5(+) stem and progenitor cells reside at the apex of a heterogeneous embryonic hepatoblast pool

Prior, N., Hindley, C. J., Rost, F., Melendez, E., Lau, W. W. Y., Gottgens, B., Rulands, S., Simons, B. D., & Huch, M. (2019). Lgr5(+) stem and progenitor cells reside at the apex of a heterogeneous embryonic hepatoblast pool. Development, 146(12):. doi:10.1242/dev.174557.

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アイテムのパーマリンク: https://hdl.handle.net/21.11116/0000-0004-9A55-F 版のパーマリンク: https://hdl.handle.net/21.11116/0000-0009-D5F0-7
資料種別: 学術論文

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 作成者:
Prior, Nicole1, 著者
Hindley, Christopher J.1, 著者
Rost, Fabian1, 著者
Melendez, Elena1, 著者
Lau, Winnie W. Y.1, 著者
Gottgens, Berthold1, 著者
Rulands, Steffen2, 著者           
Simons, Benjamin D.1, 著者
Huch, Meritxell1, 著者
所属:
1external, ou_persistent22              
2Max Planck Institute for the Physics of Complex Systems, Max Planck Society, ou_2117288              

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 MPIPKS: Living matter
 要旨: During mouse embryogenesis, progenitors within the liver known as hepatoblasts give rise to adult hepatocytes and cholangiocytes. Hepatoblasts, which are specified at E8.5-E9.0, have been regarded as a homogeneous progenitor population that initiate differentiation from E13.5. Recently, scRNA-seq analysis has identified sub-populations of transcriptionally distinct hepatoblasts at E11.5. Here, we show that hepatoblasts are not only transcriptionally but also functionally heterogeneous, and that a subpopulation of E9.5-E10.0 hepatoblasts exhibit a previously unidentified early commitment to cholangiocyte fate. Importantly, we also identify a subpopulation constituting2% of E9.5-E10.0 hepatoblasts that express the adult stem cell marker Lgr5, and generate both hepatocyte and cholangiocyte progeny that persist for the lifespan of the mouse. Combining lineage tracing and scRNA-seq, we show that Lgr5 marks E9.5-E10.0 bipotent liver progenitors residing at the apex of a hepatoblast hierarchy. Furthermore, isolated Lgr5(+) hepatoblasts can be clonally expanded in vitro into embryonic liver organoids, which can commit to either hepatocyte or cholangiocyte fates. Our study demonstrates functional heterogeneity within E9.5 hepatoblasts and identifies Lgr5 as a marker for a subpopulation of bipotent liver progenitors.

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 日付: 2019-06-122019-05-29
 出版の状態: 出版
 ページ: -
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 目次: -
 査読: -
 識別子(DOI, ISBNなど): ISI: 000473330400023
DOI: 10.1242/dev.174557
 学位: -

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出版物名: Development
  その他 : Development
種別: 学術雑誌
 著者・編者:
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出版社, 出版地: Cambridge, Cambridgeshire : Company of Biologists
ページ: - 巻号: 146 (12) 通巻号: dev174557 開始・終了ページ: - 識別子(ISBN, ISSN, DOIなど): ISSN: 0950-1991
CoNE: https://pure.mpg.de/cone/journals/resource/954927546241