The progressive changes of filamentous actin cytoskeleton in the hippocampal neurons after pilocarpine-induced status epilepticus

Epilepsy Res. 2015 Dec:118:55-67. doi: 10.1016/j.eplepsyres.2015.11.002. Epub 2015 Nov 10.

Abstract

In a previous study, we reported a persistent reduction of F-actin puncta but a compensating increase in puncta size in the mouse hippocampus at 2 months after pilocarpine-induced status epilepticus (Epilepsy Res. 108 (2014), 379-389). However, the F-actin changes during the period of epileptogenesis remain unknown. This study was designed to examine the temporal and spatial changes of F-actin during the period of epileptogenesis in a pilocarpine-induced epilepsy model, primarily by the histological and TUNEL evaluation of cell loss, phalloidin detection of F-actin, and immunohistochemical analysis of glial reactions. The results demonstrated that F-actin continued to decrease after pilocarpine treatment, which was consistent in its time course with hippocampal neuronal death. Within different hippocampal subfields, the spatial changes of F-actin exhibited similar features. First, the F-actin puncta decreased in number. Thereafter, F-actin was transiently aggregated in dendritic shafts and neuronal cell bodies and eventually was completely lost in the degenerated neurons. The progressive changes of F-actin in the degenerating neurons reported in this study may help to elucidate a cytoskeletal mechanism that may link to the delayed cell loss that occurs during epileptogenesis.

Keywords: Filamentous actin; Hippocampus; Pilocarpine; Status epilepticus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Cytoskeleton / metabolism*
  • Actins / metabolism*
  • Analysis of Variance
  • Animals
  • Calcium-Binding Proteins / metabolism
  • Cells, Cultured
  • Disease Models, Animal
  • Gene Expression Regulation / drug effects
  • Hippocampus / drug effects
  • Hippocampus / pathology*
  • In Situ Nick-End Labeling
  • Male
  • Mice
  • Mice, Inbred ICR
  • Microfilament Proteins / metabolism
  • Muscarinic Agonists / toxicity
  • Nerve Tissue Proteins / metabolism
  • Neurons / drug effects
  • Neurons / pathology*
  • Pilocarpine / toxicity
  • Status Epilepticus / chemically induced
  • Status Epilepticus / pathology*
  • Time Factors

Substances

  • Actins
  • Aif1 protein, mouse
  • Calcium-Binding Proteins
  • Microfilament Proteins
  • Muscarinic Agonists
  • Nerve Tissue Proteins
  • Pilocarpine