| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4312764 | Behavioural Brain Research | 2013 | 6 Pages |
ObjectivesThe aim of this study was to investigate whether IL-1β treatment affects F-actin in hippocampal neurons.Materials and methodsPrimary culture of hippocampal neurons were prepared from rat embryos, and the effect of different concentrations of IL-1β on the cell phenotype was investigated. Cell viability was monitored by CCK-8 activity analysis. Western blotting and immunofluorescence were performed to analyze protein levels and morphological changes in cells treated with IL-1β.ResultsIL-1β increased viability at low doses and these increases were severely blunted at higher concentrations. Similarly, the expression of F-actin was increased at low concentrations and decreased at high concentrations.ConclusionsIL-1β has a critical role in regulating hippocampal neuron viability by stimulating F-actin expression. These data suggest that IL-1β secretion at low doses is beneficial for the expression of F-actin, which can improve the survival of hippocampal neurons during stress. However,these effect were severely blunted at higher concentrations.
► IL-1β increased viability at low doses for hippocampal neurons. ► High doses IL-1β blunted increases effection of low doses for hippocampal neurons. ► IL-1β increased the expression of F-actin at low doses in hippocampal neurons. ► IL-1β decreased the expression of F-actin at high doses in hippocampal neurons.
