Resistance of neonatal primary astrocytes against Fas-induced apoptosis depends on silencing of caspase 8

Neurosci Lett. 2010 Aug 2;479(3):206-10. doi: 10.1016/j.neulet.2010.05.057. Epub 2010 May 25.

Abstract

In the present report, we have found that primary fetal astrocytes express caspase 8 and undergo apoptosis in response to Fas ligation. In contrast, neonatal astrocytes do not express detectable levels of the enzyme and are resistant to Fas killing. Fas-induced apoptosis can be restored in these cells by up-regulation of caspase 8 expression by means of transient transfection with a caspase 8-encoding plasmid. Furthermore, treatment of primary astrocytes with the demethylating agent 5-Aza-dC restores caspase 8 expression and increases the sensibility of neonatal astrocytes to the cytotoxic effect of Fas activation. Altogether, our findings indicate that silencing of caspase 8 gene is a key factor controlling the outcome of neonatal astrocytes upon Fas engagement.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Apoptosis*
  • Astrocytes / cytology*
  • Caspase 8 / biosynthesis
  • Caspase 8 / genetics*
  • Cerebral Cortex / cytology
  • Gene Silencing
  • Rats
  • Rats, Sprague-Dawley
  • Up-Regulation

Substances

  • Caspase 8