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Impact of Actin Filament Stabilization on Adult Hippocampal and Olfactory Bulb Neurogenesis

Authors :
René Jüttner
Helmut Kettenmann
Isabella Heuser
Klaus Fink
Matthias Endres
Ingo Przesdzing
Golo Kronenberg
Ferah Yildirim
Tina Baldinger
Reinhard Sohr
Karen Gertz
Shengbo Ji
Pierre Chryso Djoufack
Rainer Hellweg
Heide Hörtnagl
Sarah Eckart
Rainer Glass
Helmut Schröck
Dorette Freyer
Jitender Kumar
Imke Kirste
Source :
The Journal of Neuroscience. 30:3419-3431
Publication Year :
2010
Publisher :
Society for Neuroscience, 2010.

Abstract

Rearrangement of the actin cytoskeleton is essential for dynamic cellular processes. Decreased actin turnover and rigidity of cytoskeletal structures have been associated with aging and cell death. Gelsolin is a Ca2+-activated actin-severing protein that is widely expressed throughout the adult mammalian brain. Here, we used gelsolin-deficient (Gsn−/−) mice as a model system for actin filament stabilization. InGsn−/−mice, emigration of newly generated cells from the subventricular zone into the olfactory bulb was slowed.In vitro, gelsolin deficiency did not affect proliferation or neuronal differentiation of adult neural progenitors cells (NPCs) but resulted in retarded migration. Surprisingly, hippocampal neurogenesis was robustly induced by gelsolin deficiency. The ability of NPCs to intrinsically sense excitatory activity and thereby implement coupling between network activity and neurogenesis has recently been established. Depolarization-induced [Ca2+]iincreases and exocytotic neurotransmitter release were enhanced inGsn−/−synaptosomes. Importantly, treatment ofGsn−/−synaptosomes with mycotoxin cytochalasin D, which, like gelsolin, produces actin disassembly, decreased enhanced Ca2+influx and subsequent exocytotic norepinephrine release to wild-type levels. Similarly, depolarization-induced glutamate release fromGsn−/−brain slices was increased. Furthermore, increased hippocampal neurogenesis inGsn−/−mice was associated with a special microenvironment characterized by enhanced density of perfused vessels, increased regional cerebral blood flow, and increased endothelial nitric oxide synthase (NOS-III) expression in hippocampus. Together, reduced filamentous actin turnover in presynaptic terminals causes increased Ca2+influx and, subsequently, elevated exocytotic neurotransmitter release acting on neural progenitors. Increased neurogenesis inGsn−/−hippocampus is associated with a special vascular niche for neurogenesis.

Details

ISSN :
15292401 and 02706474
Volume :
30
Database :
OpenAIRE
Journal :
The Journal of Neuroscience
Accession number :
edsair.doi.dedup.....58a02498b1c4364e0749ff0b55a34185
Full Text :
https://doi.org/10.1523/jneurosci.4231-09.2010