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Ehm, O.K.H. ; Göritz, C.* ; Covic, M. ; Schäffner, I. ; Schwarz, T.J. ; Karaca, E. ; Kempkes, B. ; Kremmer, E. ; Pfrieger, F.W.* ; Espinosa, L.* ; Bigas, A.* ; Giachino, C.* ; Taylor, V.* ; Frisen, J.* ; Lie, D.C.

RBPJκ-dependent signaling is essential for long-term maintenance of neural stem cells in the adult hippocampus.

J. Neurosci. 30, 13794-13807 (2010)
Verlagsversion DOI
The generation of new neurons from neural stem cells in the adult hippocampal dentate gyrus contributes to learning and mood regulation. To sustain hippocampal neurogenesis throughout life, maintenance of the neural stem cell pool has to be tightly controlled. We found that the Notch/RBPJκ-signaling pathway is highly active in neural stem cells of the adult mouse hippocampus. Conditional inactivation of RBPJκ in neural stem cells in vivo resulted in increased neuronal differentiation of neural stem cells in the adult hippocampus at an early time point and depletion of the Sox2-positive neural stem cell pool and suppression of hippocampal neurogenesis at a later time point. Moreover, RBPJκ-deficient neural stem cells displayed impaired self-renewal in vitro and loss of expression of the transcription factor Sox2. Interestingly, we found that Notch signaling increases Sox2 promoter activity and Sox2 expression in adult neural stem cells. In addition, activated Notch and RBPJκ were highly enriched on the Sox2 promoter in adult hippocampal neural stem cells, thus identifying Sox2 as a direct target of Notch/RBPJκ signaling. Finally, we found that overexpression of Sox2 can rescue the self-renewal defect in RBPJκ-deficient neural stem cells. These results identify RBPJκ-dependent pathways as essential regulators of adult neural stem cell maintenance and suggest that the actions of RBPJκ are, at least in part, mediated by control of Sox2 expression.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Dentate gyrus; Progenitor cells; In-vivo; Subentricular zone; Newborn neurons; Transgenic mice; SOX2 expression; Gene knockout; Granule cells; Mouse-brain
ISSN (print) / ISBN 0270-6474
e-ISSN 1529-2401
Quellenangaben Band: 30, Heft: 41, Seiten: 13794-13807 Artikelnummer: , Supplement: ,
Verlag Society for Neuroscience
Begutachtungsstatus Peer reviewed