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Zinc and Copper Effects on Stability of Tubulin and Actin Networks in Dendrites and Spines of Hippocampal Neurons.
- Source :
-
ACS chemical neuroscience [ACS Chem Neurosci] 2017 Jul 19; Vol. 8 (7), pp. 1490-1499. Date of Electronic Publication: 2017 Apr 03. - Publication Year :
- 2017
-
Abstract
- Zinc and copper ions can modulate the activity of glutamate receptors. However, labile zinc and copper ions likely represent only the tip of the iceberg and other neuronal functions are suspected for these metals in their bound state. We performed synchrotron X-ray fluorescence imaging with 30 nm resolution to image total biometals in dendrites and spines from hippocampal neurons. We found that zinc is distributed all along the dendrites while copper is mainly pinpointed within the spines. In spines, zinc content is higher within the spine head while copper is higher within the spine neck. Such specific distributions suggested metal interactions with cytoskeleton proteins. Zinc supplementation induced the increase of β-tubulin content in dendrites. Copper supplementation impaired the β-tubulin and F-actin networks. Copper chelation resulted in the decrease of F-actin content in dendrites, drastically reducing the number of F-actin protrusions. These results indicate that zinc is involved in microtubule stability whereas copper is essential for actin-dependent stability of dendritic spines, although copper excess can impair the dendritic cytoskeleton.
- Subjects :
- Animals
Astrocytes
Cations metabolism
Cells, Cultured
Chelating Agents pharmacology
Coculture Techniques
Copper administration & dosage
Dendrites drug effects
Dermoscopy
Fluorescent Antibody Technique
Hippocampus cytology
Hippocampus drug effects
Rats, Sprague-Dawley
Spectrometry, X-Ray Emission
Zinc administration & dosage
Actins metabolism
Copper metabolism
Dendrites metabolism
Hippocampus metabolism
Tubulin metabolism
Zinc metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1948-7193
- Volume :
- 8
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- ACS chemical neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- 28323401
- Full Text :
- https://doi.org/10.1021/acschemneuro.6b00452