Cyclosporine induces neuronal apoptosis and selective oligodendrocyte death in cortical cultures

John W. McDonald, Mark P. Goldberg, Byoung J. Gwag, Shu Ing Chi, Dennis W. Choi

Research output: Contribution to journalReview article

Abstract

Cyclosporine is used clinically as an immunosuppressant, but carries a risk of central nervous system toxicity due to undefined mechanisms. We examined the ability of cyclosporine exposure to kill cultured mouse cortical neurons and gila. Mixed neuron/glial cultures exposed to 1 to 20 μM cyclosporine for 24 to 48 hours developed concentration-dependent neuronal death, with most neurons destroyed by 20 μM cyclosporine. This neuronal death was characterized by cell body shrinkage and blebbing, chromatin condensation, and internucleosomal DNA fragmentation, consistent with apoptosis. Neuronal death was reduced by addition of cycloheximide, brain- derived neurotrophic factor, or insulin-like growth factor I but not N- methyl-D-aspartate- or AMPA-type glutamate receptor antagonists. Oligodendrocytes were more sensitive to cyclosporine-induced damage than were neurons, but astrocytes were relatively resistant. Oligodendrocyte death was accompanied by positive TUNEL (terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate-biotin nick end-labeling) staining and was attenuated by application of ciliary neurotrophic factor or insulin-like growth factor I but not glutamate receptor antagonists. Present observations raise the possibility that the central nervous system toxicity syndrome associated with cyclosporine may be caused by the drug-induced death of oligodendrocytes and neurons.

Original languageEnglish (US)
Pages (from-to)750-758
Number of pages9
JournalAnnals of neurology
Volume40
Issue number5
DOIs
StatePublished - Nov 1996

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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