![[feed]](/style/images/feed-icon-14x14.png){kind=icon}
![[img]](http://edoc.mdc-berlin.de/style/images/fileicons/application_pdf.png) |
PDF
- Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
3MB |
| Item Type: | Article |
|---|---|
| Title: | Impact of actin filament stabilization on adult hippocampal and olfactory bulb neurogenesis |
| Creators Name: | Kronenberg, G. and Gertz, K. and Baldinger, T. and Kirste, I. and Eckart, S. and Yildirim, F. and Ji, S. and Heuser, I. and Schroeck, H. and Hoertnagl, H. and Sohr, R. and Djoufack, P.C. and Juettner, R. and Glass, R. and Przesdzing, I. and Kumar, J. and Freyer, D. and Hellweg, R. and Kettenmann, H. and Fink, K.B. and Endres, M. |
| 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 Ca(2+)-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. In Gsn(-/-) 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 [Ca(2+)](i) increases and exocytotic neurotransmitter release were enhanced in Gsn(-/-) synaptosomes. Importantly, treatment of Gsn(-/-) synaptosomes with mycotoxin cytochalasin D, which, like gelsolin, produces actin disassembly, decreased enhanced Ca(2+) influx and subsequent exocytotic norepinephrine release to wild-type levels. Similarly, depolarization-induced glutamate release from Gsn(-/-) brain slices was increased. Furthermore, increased hippocampal neurogenesis in Gsn(-/-) 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 Ca(2+) influx and, subsequently, elevated exocytotic neurotransmitter release acting on neural progenitors. Increased neurogenesis in Gsn(-/-) hippocampus is associated with a special vascular niche for neurogenesis. |
| Keywords: | Calcium Signaling, Cell Movement, Cerebrovascular Circulation, Cytochalasin D, Gelsolin, Hippocampus, Lateral Ventricles, Membrane Potentials, Microfilaments, Neurogenesis, Neurons, Neurotoxins, Nitric Oxide Synthase Type III, Norepinephrine, Nucleic Acid Synthesis Inhibitors, Olfactory Bulb, Organ Culture Techniques, Presynaptic Terminals, Stem Cells, Synaptosomes, Animals, Mice |
| Source: | Journal of Neuroscience |
| ISSN: | 0270-6474 |
| Publisher: | Society for Neuroscience |
| Volume: | 30 |
| Number: | 9 |
| Page Range: | 3419-3431 |
| Date: | 3 March 2010 |
| Official Publication: | https://doi.org/10.1523/JNEUROSCI.4231-09.2010 |
| PubMed: | View item in PubMed |
Repository Staff Only: item control page
Download Statistics
Download Statistics
