β-Catenin Signaling Promotes Proliferation of Progenitor Cells in the Adult Mouse Subventricular Zone

Author:

Adachi Kazuhide123,Mirzadeh Zaman4,Sakaguchi Masanori3,Yamashita Toru523,Nikolcheva Tania6,Gotoh Yukiko7,Peltz Gary6,Gong Leyi8,Kawase Takeshi1,Alvarez-Buylla Arturo4,Okano Hideyuki3,Sawamoto Kazunobu923

Affiliation:

1. Department of Neurosurgery, Keio University School of Medicine, Tokyo, Japan

2. Bridgestone Laboratory of Developmental and Regenerative Neurobiology, Keio University School of Medicine, Tokyo, Japan

3. Department of Physiology, Keio University School of Medicine, Tokyo, Japan

4. Department of Neurological Surgery and Program in Developmental and Stem Cell Biology, University of California San Francisco, San Francisco, California, USA

5. Department of Neurology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama, Japan

6. Departments of Genetics and Genomics, University of Tokyo, Tokyo, Japan

7. Institute of Molecular and Cellular Biosciences, University of Tokyo, Tokyo, Japan

8. Department of Chemistry, Roche Palo Alto, Palo Alto, California, USA

9. Department of Developmental and Regenerative Biology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan

Abstract

Abstract The subventricular zone (SVZ) is the largest germinal zone in the mature rodent brain, and it continuously produces young neurons that migrate to the olfactory bulb. Neural stem cells in this region generate migratory neuroblasts via highly proliferative transit-amplifying cells. The Wnt/β-catenin signaling pathway partially regulates the proliferation and neuronal differentiation of neural progenitor cells in the embryonic brain. Here, we studied the role of β-catenin signaling in the adult mouse SVZ. β-Catenin-dependent expression of a destabilized form of green fluorescent protein was detected in progenitor cells in the adult SVZ of Axin2-d2EGFP reporter mice. Retrovirus-mediated expression of a stabilized β-catenin promoted the proliferation of Mash1+ cells and inhibited their differentiation into neuroblasts. Conversely, the expression of Dkk1, an inhibitor of Wnt signaling, reduced the proliferation of Mash1+ cells. In addition, an inhibitor of GSK3β promoted the proliferation of Mash1+ cells and increased the number of new neurons in the olfactory bulb 14 days later. These results suggest that β-catenin signaling plays a role in the proliferation of progenitor cells in the SVZ of the adult mouse brain. Disclosure of potential conflicts of interest is found at the end of this article.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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