Two-Photon Correlation Spectroscopy in Single Dendritic Spines Reveals Fast Actin Filament Reorganization during Activity-Dependent Growth

PLoS One. 2015 May 28;10(5):e0128241. doi: 10.1371/journal.pone.0128241. eCollection 2015.

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 fraction of the actin filament population that was already present before spine head growth.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Cytoskeleton / genetics
  • Actin Cytoskeleton / metabolism
  • Actin Cytoskeleton / ultrastructure*
  • Actins / chemistry*
  • Actins / classification
  • Actins / genetics
  • Actins / metabolism
  • Animals
  • Animals, Newborn
  • CA3 Region, Hippocampal / drug effects
  • CA3 Region, Hippocampal / metabolism
  • CA3 Region, Hippocampal / ultrastructure*
  • Dendritic Spines / drug effects
  • Dendritic Spines / genetics
  • Dendritic Spines / metabolism
  • Dendritic Spines / ultrastructure*
  • Gene Expression
  • Long-Term Potentiation / physiology
  • Mice
  • Mice, Inbred C57BL
  • Primary Cell Culture
  • Spectrometry, Fluorescence / methods
  • Tetraethylammonium / pharmacology

Substances

  • Actins
  • Tetraethylammonium

Grants and funding

This work was partially supported by the German Research Foundation to MK and MZ (DFG-ZA554/2-1). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.