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Return to quiescence of mouse neural stem cells by degradation of a proactivation protein

15 juil. 2016Science

DOI : 10.1126/science.aaf4802

Auteurs

Noelia Urbán, Debbie L. C. van den Berg, Antoine Forget, Jimena Andersen, Jeroen A. A. Demmers, Charles Hunt, Olivier Ayrault, François Guillemot

Résumé

Sending neural stem cells back to the garage

In the brain's hippocampus, which modulates memories and emotions, neural stem cells generate new neurons, even during adulthood. How many new neurons are generated, and when, follows from the balance between quiescence and proliferation in the pool of neural stem cells. Urbán et al. asked what signals send proliferating stem cells back into a quiescent state. They found that a key transcription factor that promotes cellular proliferation was degraded through the ubiquitinylation system. This molecular interaction regulated the return to a resting state, but one that was not quite as quiescent as the original state. Stem cells in this resting but primed state sustained the stem cell pool.

Science , this issue p. 292

Membres

OLIVIER AYRAULT

Directeur de recherche CNRS