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Emergence and patterning dynamics of mouse-definitive endoderm.
Pour, Maayan; Kumar, Abhishek Sampath; Farag, Naama; Bolondi, Adriano; Kretzmer, Helene; Walther, Maria; Wittler, Lars; Meissner, Alexander; Nachman, Iftach.
Afiliación
  • Pour M; School of Neurobiology, Biochemistry and Biophysics, Department of Biochemistry and Molecular Biology, Tel Aviv University, Tel Aviv 6997801, Israel.
  • Kumar AS; Department of Genome Regulation, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany.
  • Farag N; School of Neurobiology, Biochemistry and Biophysics, Department of Biochemistry and Molecular Biology, Tel Aviv University, Tel Aviv 6997801, Israel.
  • Bolondi A; Department of Genome Regulation, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany.
  • Kretzmer H; Department of Genome Regulation, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany.
  • Walther M; Department of Genome Regulation, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany.
  • Wittler L; Department of Developmental Genetics, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany.
  • Meissner A; Department of Genome Regulation, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany.
  • Nachman I; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
iScience ; 25(1): 103556, 2022 Jan 21.
Article en En | MEDLINE | ID: mdl-34988400
ABSTRACT
The segregation of definitive endoderm (DE) from bipotent mesendoderm progenitors leads to the formation of two distinct germ layers. Dissecting DE commitment and onset has been challenging as it occurs within a narrow spatiotemporal window in the embryo. Here, we employ a dual Bra/Sox17 reporter cell line to study DE onset dynamics. We find Sox17 expression initiates in vivo in isolated cells within a temporally restricted window. In 2D and 3D in vitro models, DE cells emerge from mesendoderm progenitors at a temporally regular, but spatially stochastic pattern, which is subsequently arranged by self-sorting of Sox17 + cells. A subpopulation of Bra-high cells commits to a Sox17+ fate independent of external Wnt signal. Self-sorting coincides with upregulation of E-cadherin but is not necessary for DE differentiation or proliferation. Our in vivo and in vitro results highlight basic rules governing DE onset and patterning through the commonalities and differences between these systems.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: IScience Año: 2022 Tipo del documento: Article País de afiliación: Israel

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: IScience Año: 2022 Tipo del documento: Article País de afiliación: Israel
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