Key result
NMDA receptor antagonism reduces truncated apoE-induced intracellular calcium overload and neuronal cell death in culture.
Answers are grounded in this paper and cite their sources.
Apolipoprotein E (apoE)-related synthetic peptides, the 22 kDa N-terminal thrombin-cleavage fragment of apoE (truncated apoE), and full-length apoE have all been shown to exhibit neurotoxic activity under certain culture conditions. In the present study, protease inhibitors reduced the neurotoxicity and proteolysis of full-length apoE but did not block the toxicity of truncated apoE or a synthetic apoE peptide, suggesting that fragments of apoE may account for its toxicity. Additional experiments demonstrated that both truncated apoE and the apoE peptide elicit an increase in intracellular calcium levels and subsequent death of embryonic rat hippocampal neurons in culture. Similar effects on calcium were found when the apoE peptide was applied to chick sympathetic neurons. The rise in intracellular calcium and the hippocampal cell death caused by the apoE peptide were significantly reduced by receptor-associated protein, removal of extracellular calcium, or administration of the specific NMDA glutamate receptor antagonist MK-801. These results suggest that apoE may be a source of both neurotoxicity and calcium influx that involves cell surface receptors. Such findings strengthen the hypothesis that apoE plays a direct role in the pathology of Alzheimer's disease.
No takes yet. Share an insight, caveat, or question.
Tolar et al. (1999) studied Neurotoxicity / Alzheimer's disease pathology. Truncated apoE and synthetic apoE peptide vs. Full-length apoE or untreated conditions was evaluated on Intracellular calcium levels and neuronal cell death. Truncated apoE and synthetic apoE peptide increased intracellular calcium and caused neuronal death in culture, which was reduced by the specific NMDA glutamate receptor antagonist MK-801.
Synapse has enriched 10 related papers. Consider them for comparative context: