Mapping spatio-temporal activation of Notch signaling during neurogenesis and gliogenesis in the developing mouse brain

Authors

  • Akinori Tokunaga,

    1. Department of Physiology, Keio University School of Medicine, Tokyo, Japan
    2. Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency, Saitama, Japan
    3. Osaka University Graduate School of Medicine, Suita, Osaka, Japan
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  • Jun Kohyama,

    1. Department of Physiology, Keio University School of Medicine, Tokyo, Japan
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  • Tetsu Yoshida,

    1. Department of Physiology, Keio University School of Medicine, Tokyo, Japan
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  • Keiko Nakao,

    1. Department of Physiology, Keio University School of Medicine, Tokyo, Japan
    2. Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency, Saitama, Japan
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  • Kazunobu Sawamoto,

    1. Department of Physiology, Keio University School of Medicine, Tokyo, Japan
    2. Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency, Saitama, Japan
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  • Hideyuki Okano

    1. Department of Physiology, Keio University School of Medicine, Tokyo, Japan
    2. Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency, Saitama, Japan
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Address correspondence and reprint requests to H. Okano, Department of Physiology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160–8582, Japan.
E-mail: hidokano@sc.itc.keio.ac.jp

Abstract

Notch1 plays various important roles including the maintenance of the stem cell state as well as the promotion of glial fates in mammalian CNS development. However, because of the very low amount of the activated form of Notch1 present in vivo, its precise activation pattern has remained unknown. In this study, we mapped the active state of this signaling pathway in situ in the developing mouse brain using a specific antibody that recognizes the processed form of the intracellular domain of Notch1 cleaved by presenilin/γ-secretase activity. By using this antibody, active state of Notch1 came to be detectable with a higher sensitivity than using conventional antibody against Notch1. We found that activated Notch1 was mainly detected in the nuclei of a subpopulation of radial glial cells, the majority of proliferating precursor cells in the ventricular zone (VZ). However, Notch1 activation was not detected in neuronal precursor cells positive for neuronal basic helix-loop-helix proteins or in differentiating neurons in the embryonic forebrain. Interestingly, we found that Notch1 was transiently activated in the astrocytic lineage during perinatal CNS development. Taken together, the present method has enabled us to determine the timing, gradients, and boundaries of the activation of Notch signaling.

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