Beta-Catenin Signaling Negatively Regulates Intermediate Progenitor Population Numbers in the Developing Cortex |
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Authors: | Christopher A. Mutch Jessica D. Schulte Eric Olson Anjen Chenn |
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Affiliation: | 1. Department of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, United States of America.; 2. Department of Neuroscience and Physiology, State University of New York, Upstate Medical University, Syracuse, New York, United States of America.;Universidade Federal do Rio de Janeiro, Brazil |
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Abstract: | Intermediate progenitor cells constitute a second proliferative cell type in the developing mammalian cerebral cortex. Little is known about the factors that govern the production of intermediate progenitors. Although persistent expression of stabilized β-catenin was found to delay the maturation of radial glial progenitors into intermediate progenitors, the relationship between β-catenin signaling and intermediate progenitors remains poorly understood. Using a transgenic reporter mouse for Axin2, a direct target of Wnt/β-catenin signaling, we observed that β-catenin signaling is decreased in intermediate progenitor cells relative to radial glial progenitors. Conditional deletion of β-catenin from mouse cortical neural progenitors increased intermediate progenitor numbers, while conditional expression of stabilized β-catenin reduced the intermediate progenitor population. Together, these findings provide evidence that β-catenin signaling in radial progenitors negatively regulates intermediate progenitor cell number during cortical development. |
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