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Assessing Cell Cycle Progression of Neural Stem and Progenitor Cells in the Mouse Developing Brain after Genotoxic Stress
Published on: May 7, 2014
Neural stem and progenitor cells shorten S-phase on commitment to neuron production
Yoko Arai1, Jeremy N Pulvers, Christiane Haffner
1Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307 Dresden, Germany.
Nature Communications
|January 13, 2011
Summary
Neural stem and progenitor cells lengthen their cell cycle G1-phase during brain development. Expanding progenitors spend more time in S-phase for DNA quality control before committing to neuron production.
Area of Science:
- Neuroscience
- Developmental Biology
- Cell Biology
Background:
- Cell cycle regulation is crucial for mammalian cerebral cortex development.
- Lengthening of the G1-phase of the cell cycle is observed, but the specific neural stem and progenitor cells affected remain unclear.
Purpose of the Study:
- To develop a novel method for determining cell-cycle parameters in specific neural stem and progenitor cell classes.
- To identify which neural progenitor populations exhibit G1-phase lengthening during cerebral cortex development.
Main Methods:
- Utilized molecular markers to classify neural stem and progenitor cells, rather than relying on their location.
- Measured cell-cycle parameters, including G1 and S-phase duration, in distinct progenitor populations.
- Performed comparative genome-wide gene expression analysis.
Main Results:
- G1-phase lengthening is associated with the transition from apical progenitors to basal progenitors.
- Expanding apical and basal progenitors have a significantly longer S-phase compared to committed progenitors.
- Gene expression analysis revealed alterations in cell-cycle regulation, DNA replication/repair, and chromatin remodeling factors.
Conclusions:
- Expanding neural stem and progenitor cells allocate more S-phase time to DNA quality control compared to progenitors committed to neuron production.
- These findings provide new insights into the cell-cycle regulation strategies during mammalian brain development.
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