benzyloxycarbonylvalyl-alanyl-aspartyl-fluoromethyl-ketone and stearic-acid

Apoptotic cell death has been proposed to play a role in the neuronal loss observed following traumatic injury in the CNS and PNS. The present study uses an in vitro tissue culture model to investigate whether free fatty acids (FFAs), at concentrations comparable to those found following traumatic brain injury, trigger cell death. Nerve growth factor (NGF)-differentiated PC12 cells exposed to oleic and arachidonic acids (2 : 1 ratio FFA/BSA) showed normal cell survival. However, when cells were exposed to stearic and palmitic acids, there was a dramatic loss of cell viability after 24 h of treatment. The cell death induced by stearic acid and palmitic acid was apoptotic as assessed by morphological analysis, and activation of caspase-8 and caspase-3-like activities. Western blotting showed that differentiated PC12 cells exposed to stearic and palmitic acids exhibited the signature apoptotic cleavage fragment of poly (ADP-ribose) polymerase (PARP). Interestingly, blockade of caspase activities with the pan-caspase inhibitor z-VAD-fmk failed to prevent the cell death observed induced by palmitic or stearic acid. RT-PCR and RNA blot experiments showed an up-regulation of the Fas receptor and ligand mRNA. These findings are consistent with our hypothesis that FFAs may play a role in the cell death associated with trauma in the CNS and PNS.

Topics: Amino Acid Chloromethyl Ketones; Animals; Apoptosis; Arachidonic Acid; Caspase 3; Caspase 8; Caspase 9; Caspase Inhibitors; Caspases; Cell Differentiation; Cell Survival; DNA Fragmentation; Enzyme Inhibitors; Fas Ligand Protein; fas Receptor; Membrane Glycoproteins; Nerve Growth Factor; Neurons; Oleic Acid; Palmitic Acid; PC12 Cells; Poly(ADP-ribose) Polymerases; Rats; RNA, Messenger; Stearic Acids