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Schäffner, I.* ; Minakaki, G.* ; Khan, M.A. ; Balta, E.A.* ; Schlötzer-Schrehardt, U.* ; Schwarz, T.J. ; Beckervordersandforth, R.* ; Winner, B.* ; Webb, A.E.* ; DePinho, R.A.* ; Paik, J.* ; Wurst, W. ; Klucken, J.* ; Lie, D.C.C.*

FoxO function is essential for maintenance of autophagic flux and neuronal morphogenesis in adult neurogenesis.

Neuron 99, 1188-1203.e6 (2018)
Verlagsversion DOI
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Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Autophagy is a conserved catabolic pathway with emerging functions in mammalian neurodevelopment and human neurodevelopmental diseases. The mechanisms controlling autophagy in neuronal development are not fully understood. Here, we found that conditional deletion of the Forkhead Box O transcription factors FoxO1, FoxO3, and FoxO4 strongly impaired autophagic flux in developing neurons of the adult mouse hippocampus. Moreover, FoxO deficiency led to altered dendritic morphology, increased spine density, and aberrant spine positioning in adult-generated neurons. Strikingly, pharmacological induction of autophagy was sufficient to correct abnormal dendrite and spine development of FoxO-deficient neurons. Collectively, these findings reveal a novel link between FoxO transcription factors, autophagic flux, and maturation of developing neurons.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Foxo ; Adult Neurogenesis ; Aging ; Autism ; Autophagy ; Hippocampus ; Spines ; Stem Cells; Neural Stem-cells; Autism Spectrum Disorders; Dentate Granule Cells; In-vivo; Transcription Factors; Mammalian Autophagy; Alzheimers-disease; Homeostasis; Clearance; Degradation
ISSN (print) / ISBN 0896-6273
e-ISSN 1097-4199
Zeitschrift Neuron
Quellenangaben Band: 99, Heft: 6, Seiten: 1188-1203.e6 Artikelnummer: , Supplement: ,
Verlag Cell Press
Verlagsort Cambridge, Mass.
Begutachtungsstatus Peer reviewed