A Critical Role for Sox9 in Notch-Induced Astrogliogenesis and Stem Cell Maintenance§

Authors

  • Simone Martini,

    1. Department of Biochemistry, Medical Faculty, Christian-Albrechts-University Kiel, Kiel, Germany
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  • Kristina Bernoth,

    1. Department of Biochemistry, Medical Faculty, Christian-Albrechts-University Kiel, Kiel, Germany
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  • Heather Main,

    1. Department of Cell and Molecular Biology, Karolinska Institute, Stockholm, Sweden
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  • German Dario Camargo Ortega,

    1. Department of Cell and Molecular Biology, Karolinska Institute, Stockholm, Sweden
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  • Urban Lendahl,

    1. Department of Cell and Molecular Biology, Karolinska Institute, Stockholm, Sweden
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  • Ursula Just,

    Corresponding author
    1. Department of Biochemistry, Medical Faculty, Christian-Albrechts-University Kiel, Kiel, Germany
    • Ursula Just, Department of Biochemistry, Christian-Albrechts-University of Kiel, Olshausenstr. 40, 24098 Kiel, Germany

      Ralf Schwanbeck, Department of Biochemistry, Christian-Albrechts-University of Kiel, Olshausenstr. 40, 24098 Kiel, Germany

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    • Telephone: +49-431-880-2513; Fax: +49-431-880-2609

  • Ralf Schwanbeck

    Corresponding author
    1. Department of Biochemistry, Medical Faculty, Christian-Albrechts-University Kiel, Kiel, Germany
    • Ursula Just, Department of Biochemistry, Christian-Albrechts-University of Kiel, Olshausenstr. 40, 24098 Kiel, Germany

      Ralf Schwanbeck, Department of Biochemistry, Christian-Albrechts-University of Kiel, Olshausenstr. 40, 24098 Kiel, Germany

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    • Telephone: +49-431-880-2513; Fax: +49-431-880-2609


  • Author contributions: S.M.: collection and assembly of data, data analysis and interpretation, and final approval of manuscript; K.B., H.M., and G.D.C.O.: collection and/or assembly of data and final approval of manuscript; U.L.: data analysis and interpretation, manuscript writing, financial support, and final approval of manuscript; U.J.: concept and design, data analysis and interpretation, provision of study materials, manuscript writing, financial support, and final approval of manuscript; R.S.: Concept and design, collection and/or assembly of data, data analysis and interpretation, manuscript writing, and final approval of manuscript.

  • Disclosure of potential conflicts of interest is found at the end of this article.

  • §

    First published online in STEM CELLS EXPRESS January 10, 2013.

Abstract

Notch signaling is a key regulator of cell-fate decisions and is essential for proper neuroectodermal development. There, it favors the formation of ectoderm, promotes maintenance of neural stem cells, inhibits differentiation into neurons, and commits neural progenitors to a glial fate. In this report, we explore downstream effects of Notch important for astroglial differentiation. Transient activation of Notch1 during early stages of neuroectodermal differentiation of embryonic stem cells resulted in an increase of neural stem cells, a reduction in neurons, an induction of astroglial cell differentiation, and an induction of neural crest (NC) development. Transient or continuous activation of Notch1 during neuroectodermal differentiation led to upregulation of Sox9 expression. Knockdown of the Notch1-induced Sox9 expression reversed Notch1-induced astroglial cell differentiation, increase in neural stem cells, and the decrease in neurons, whereas the Notch1 effects on NC development were hardly affected by knockdown of Sox9 expression. These findings reveal a critical role for Notch-mediated upregulation of Sox9 in a select set of neural lineage determination steps controlled by Notch. STEM CELLS 2013;31:741–751

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