Forced G1-phase reduction alters mode of division, neuron number, and laminar phenotype in the cerebral cortex
| Autor: | Sabina Pfister, Edouard Ollier, Louis-Jan Pilaz, Rodney J. Douglas, Elodie Gautier, Veronique Cortay, Colette Dehay, Henry Kennedy, Nathalie Doerflinger, Marion Betizeau, Guillaume Marcy, Dorothée Patti |
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| Rok vydání: | 2009 |
| Předmět: |
Cell division
PAX6 Transcription Factor Subventricular zone Biology Mice Pregnancy medicine Animals Paired Box Transcription Factors RNA Small Interfering Eye Proteins Genetics Cerebral Cortex Homeodomain Proteins Neurons Multidisciplinary Base Sequence Neurogenesis G1 Phase Biological Sciences Cell biology Repressor Proteins Corticogenesis Cyclin E1 medicine.anatomical_structure Electroporation Phenotype Cerebral cortex Female Neuron PAX6 Cell Division |
| Zdroj: | Proceedings of the National Academy of Sciences of the United States of America. 106(51) |
| ISSN: | 1091-6490 |
| Popis: | The link between cortical precursors G1 duration (TG1) and their mode of division remains a major unresolved issue of potential importance for regulating corticogenesis. Here, we induced a 25% reduction in TG1 in mouse cortical precursors via forced expression of cyclin D1 and cyclin E1. We found that in utero electroporation-mediated gene transfer transfects a cohort of synchronously cycling precursors, necessitating alternative methods of measuring cell-cycle phases to those classical used. TG1 reduction promotes cell-cycle reentry at the expense of differentiation and increases the self-renewal capacities of Pax6 precursors as well as of Tbr2 basal precursors (BPs). A population level analysis reveals sequential and lineage-specific effects, showing that TG1 reduction: ( i ) promotes Pax6 self-renewing proliferative divisions before promoting divisions wherein Pax6 precursors generate Tbr2 BPs and ( ii ) promotes self-renewing proliferative divisions of Tbr2 precursors at the expense of neurogenesis, thus leading to an amplification of the BPs pool in the subventricular zone and the dispersed mitotic compartment of the intermediate zone. These results point to the G1 mode of division relationship as an essential control mechanism of corticogenesis. This is further supported by long-term studies showing that TG1 reduction results in cytoarchitectural modifications including supernumerary supragranular neuron production. Modeling confirms that the TG1-induced changes in neuron production and laminar fate are mediated via the changes in the mode of division. These findings also have implications for understanding the mechanisms that have contributed to brain enlargement and complexity during evolution. |
| Databáze: | OpenAIRE |
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