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Two-photon correlation spectroscopy in single dendritic spines reveals fast actin filament reorganization during activity-dependent growth.

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Chen,  J.
Research Group of Biomolecular Spectroscopy and Single-Molecule Detection, MPI for Biophysical Chemistry, Max Planck Society;

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Grunwald,  M.
Research Group of Biomolecular Spectroscopy and Single-Molecule Detection, MPI for Biophysical Chemistry, Max Planck Society;

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Walla,  P. J.
Research Group of Biomolecular Spectroscopy and Single-Molecule Detection, MPI for Biophysical Chemistry, Max Planck Society;

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Citation

Chen, J., Kellner, Y., Zagrebelsky, M., Grunwald, M., Korte, M., & Walla, P. J. (2015). Two-photon correlation spectroscopy in single dendritic spines reveals fast actin filament reorganization during activity-dependent growth. PLoS One, 10(5): e0128241. doi:10.1371/journal.pone.0128241.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0027-A679-C
Abstract
Two-photon fluorescence correlation spectroscopy (2P-FCS) within single dendritic spines of living hippocampal pyramidal neurons was used to resolve various subpopulations of mobile F-actin during activity-dependent structural changes such as potentiation induced spine head growth. Two major classes of mobile F-actin were discovered: very dynamic and about a hundred times less dynamic F-actin. Spine head enlargement upon application of Tetraethylammonium (TEA), a protocol previously used for the chemical induction of long-term potentiation (cLTP) strictly correlated to changes in the dynamics and filament numbers in the different actin filament fractions. Our observations suggest that spine enlargement is governed by a mechanism in which longer filaments are first cut into smaller filaments that cooperate with the second, increasingly dynamic shorter actin filament population to quickly reorganize and expand the actin cytoskeleton within the spine head. This process would allow a fast and efficient spine head enlargement using a major fr