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  ROS Dynamics Delineate Functional States of Hippocampal Neural Stem Cells and Link to Their Activity-Dependent Exit from Quiescence.

Adusumilli, V. S., Walker, T. L., Overall, R. W., Klatt, G. M., Zeidan, S. A., Zocher, S., et al. (2021). ROS Dynamics Delineate Functional States of Hippocampal Neural Stem Cells and Link to Their Activity-Dependent Exit from Quiescence. Cell stem cell, 28(2), 300-314. doi:10.1016/j.stem.2020.10.019.

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Adusumilli, Vijay S, Autor
Walker, Tara L, Autor
Overall, Rupert W, Autor
Klatt, Gesa M, Autor
Zeidan, Salma A, Autor
Zocher, Sara, Autor
Kirova, Dilyana G, Autor
Ntitsias, Konstantinos, Autor
Fischer, Tim J, Autor
Sykes, Alex1, Autor           
Reinhardt, Susanne, Autor
Dahl, Andreas, Autor
Mansfeld, Jorg, Autor
Rünker, Annette E, Autor
Kempermann, Gerd, Autor
Affiliations:
1Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society, ou_2340692              

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 Zusammenfassung: Cellular redox states regulate the balance between stem cell maintenance and activation. Increased levels of intracellular reactive oxygen species (ROS) are linked to proliferation and lineage specification. In contrast to this general principle, we here show that in the hippocampus of adult mice, quiescent neural precursor cells (NPCs) maintain the highest ROS levels (hiROS). Classifying NPCs on the basis of cellular ROS content identified distinct functional states. Shifts in ROS content primed cells for a subsequent state transition, with lower ROS content marking proliferative activity and differentiation. Physical activity, a physiological activator of adult hippocampal neurogenesis, recruited hiROS NPCs into proliferation via a transient Nox2-dependent ROS surge. In the absence of Nox2, baseline neurogenesis was unaffected, but the activity-induced increase in proliferation disappeared. These results provide a metabolic classification of NPC functional states and describe a mechanism linking the modulation of cellular ROS by behavioral cues to the activation of adult NPCs.

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 Datum: 2021-02-04
 Publikationsstatus: Erschienen
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 Ort, Verlag, Ausgabe: -
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 Art der Begutachtung: -
 Identifikatoren: DOI: 10.1016/j.stem.2020.10.019
Anderer: cbg-8136
PMID: 33275875
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Titel: Cell stem cell
  Andere : Cell Stem Cell
Genre der Quelle: Zeitschrift
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Affiliations:
Ort, Verlag, Ausgabe: -
Seiten: - Band / Heft: 28 (2) Artikelnummer: - Start- / Endseite: 300 - 314 Identifikator: -