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Published in: Brain Structure and Function 1/2019

Open Access 01-01-2019 | Original Article

Deficiency of the clock gene Bmal1 affects neural progenitor cell migration

Authors: Amira A. H. Ali, Beryl Schwarz-Herzke, Shakila Mir, Benita Sahlender, Marion Victor, Boris Görg, Martin Schmuck, Katharina Dach, Ellen Fritsche, Andreas Kremer, Charlotte von Gall

Published in: Brain Structure and Function | Issue 1/2019

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Abstract

We demonstrate the impact of a disrupted molecular clock in Bmal1-deficient (Bmal1−/−) mice on migration of neural progenitor cells (NPCs). Proliferation of NPCs in rostral migratory stream (RMS) was reduced in Bmal1−/− mice, consistent with our earlier studies on adult neurogenesis in hippocampus. However, a significantly higher number of NPCs from Bmal1−/− mice reached the olfactory bulb as compared to wild-type littermates (Bmal1+/+ mice), indicating a higher migration velocity in Bmal1−/− mice. In isolated NPCs from Bmal1−/− mice, not only migration velocity and expression pattern of genes involved in detoxification of reactive oxygen species were affected, but also RNA oxidation of catalase was increased and catalase protein levels were decreased. Bmal1+/+ migration phenotype could be restored by treatment with catalase, while treatment of NPCs from Bmal1+/+ mice with hydrogen peroxide mimicked Bmal1−/− migration phenotype. Thus, we conclude that Bmal1 deficiency affects NPC migration as a consequence of dysregulated detoxification of reactive oxygen species.
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Metadata
Title
Deficiency of the clock gene Bmal1 affects neural progenitor cell migration
Authors
Amira A. H. Ali
Beryl Schwarz-Herzke
Shakila Mir
Benita Sahlender
Marion Victor
Boris Görg
Martin Schmuck
Katharina Dach
Ellen Fritsche
Andreas Kremer
Charlotte von Gall
Publication date
01-01-2019
Publisher
Springer Berlin Heidelberg
Published in
Brain Structure and Function / Issue 1/2019
Print ISSN: 1863-2653
Electronic ISSN: 1863-2661
DOI
https://doi.org/10.1007/s00429-018-1775-1

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