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  Defining the Identity and Dynamics of Adult Gastric Isthmus Stem Cells.

Han, S., Fink, J., Jörg, D. J., Lee, E., Yum, M. K., Chatzeli, L., et al. (2019). Defining the Identity and Dynamics of Adult Gastric Isthmus Stem Cells. Cell stem cell, 25(3), 342-356. doi:10.1016/j.stem.2019.07.008.

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Han, Seungmin, Autor
Fink, Juergen, Autor
Jörg, David J., Autor
Lee, Eunmin, Autor
Yum, Min Kyu, Autor
Chatzeli, Lemonia, Autor
Merker, Sebastian R, Autor
Josserand, Manon, Autor
Trendafilova, Teodora, Autor
Andersson-Rolf, Amanda, Autor
Dabrowska, Catherine, Autor
Kim, Hyunki, Autor
Naumann, Ronald1, Autor           
Lee, Ji-Hyun, Autor
Sasaki, Nobuo, Autor
Mort, Richard Lester, Autor
Basak, Onur, Autor
Clevers, Hans, Autor
Stange, Daniel E, Autor
Philpott, Anna, Autor
Kim, Jong Kyoung, AutorSimons, Benjamin D, AutorKoo, Bon-Kyoung, Autor mehr..
Affiliations:
1Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society, ou_2340692              

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 Zusammenfassung: The gastric corpus epithelium is the thickest part of the gastrointestinal tract and is rapidly turned over. Several markers have been proposed for gastric corpus stem cells in both isthmus and base regions. However, the identity of isthmus stem cells (IsthSCs) and the interaction between distinct stem cell populations is still under debate. Here, based on unbiased genetic labeling and biophysical modeling, we show that corpus glands are compartmentalized into two independent zones, with slow-cycling stem cells maintaining the base and actively cycling stem cells maintaining the pit-isthmus-neck region through a process of "punctuated" neutral drift dynamics. Independent lineage tracing based on Stmn1 and Ki67 expression confirmed that rapidly cycling IsthSCs maintain the pit-isthmus-neck region. Finally, single-cell RNA sequencing (RNA-seq) analysis is used to define the molecular identity and lineage relationship of a single, cycling, IsthSC population. These observations define the identity and functional behavior of IsthSCs.

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 Datum: 2019-09-05
 Publikationsstatus: Erschienen
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 Ort, Verlag, Ausgabe: -
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 Art der Begutachtung: -
 Identifikatoren: DOI: 10.1016/j.stem.2019.07.008
Anderer: cbg-7480
PMID: 31422913
 Art des Abschluß: -

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Titel: Cell stem cell
  Andere : Cell Stem Cell
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: -
Seiten: - Band / Heft: 25 (3) Artikelnummer: - Start- / Endseite: 342 - 356 Identifikator: -