Cellular and subcellular calcium accumulation during glutamate-induced injury in cerebellar granule neurons

Manus W. Ward*, Yulia Kushnareva, Sam Greenwood, Christopher N. Connolly

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    35 Scopus citations

    Abstract

    We have investigated the role of Ca2+ accumulation and neuronal injury in cerebellar granule neurons after glutamate receptor overactivation. After the removal of the free cytosolic Ca2+ we identified an extensive second Ca2+ fraction (SCF) that is retained within the neurons after glutamate receptor overactivation. The SCF reaches a plateau within 10 min with the magnitude of this SCF accumulation reflecting the extent of the neuronal injury that occurs within the neurons. The existence of this SCF is sensitive to both NMDA receptor antagonists and mitochondrial inhibitors but is unaffected by agents that deplete endoplasmic reticulum Ca2+, indicating that this Ca2+ fraction may be located within the mitochondria. Through the isolation of mitochondria from cerebellar granule neurons treated with glutamate we have shown that the majority of the SCF is mitochondrial in location. On the removal of the glutamate stimulus the SCF recovers at a slower rate than the free Ca2+ concentration within the neuron. This is intriguing, as it implies a capacity to remember previous excitatory events. Most significantly we have shown that a short pre-application of subthreshold glutamate or kainate blocks both SCF Ca2+ accumulation and extensive neuronal injury in response to high concentrations of glutamate. These findings may be relevant to the observations of pre-conditioning in the brain and heart.

    Original languageEnglish (US)
    Pages (from-to)1081-1090
    Number of pages10
    JournalJournal of Neurochemistry
    Volume92
    Issue number5
    DOIs
    StatePublished - Mar 1 2005

    Keywords

    • Calcium
    • Glutamate
    • Kainate
    • Mitochondria
    • NMDA
    • Pre-conditioning

    ASJC Scopus subject areas

    • Biochemistry
    • Cellular and Molecular Neuroscience

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