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Cell Mol Life Sci ; 62(2): 227-38, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15666094

ABSTRACT

Many have hypothesized that cell death in Parkinson's disease is via apoptosis and, specifically, by the mitochondrial-mediated apoptotic pathway. We tested this hypothesis using a mouse dopaminergic cell line of mesencephalic origin, MN9D, challenged with the Parkinsonism-causing neurotoxin MPP+ (1-methyl-4-phenylpyridinium ion). Apoptosis was the main mode of cell death when the cells were subjected to MPP+ treatment under serum-free conditions for 24 h. Caspase-3 and caspase-9, however, were not activated, thus indicating the existence of alternate or compensatory cell death pathway(s) in dopaminergic neuronal cells. Using caspase inhibitors, we demonstrated that these pathways involve caspase-2, -8, -6 and -7. A time-course study indicated that activation of caspase-2 and -8 occurred upstream of caspase-6 and caspase-7. Upon MPP+ challenge, the apoptosis-inducing factor was translocated from the mitochondria into the MN9D cytosol and nucleus. These results suggest the existence of alternative apoptotic pathways in dopaminergic neurons.


Subject(s)
Apoptosis , Caspases/metabolism , Dopamine/metabolism , Neurons/cytology , Neurons/enzymology , 1-Methyl-4-phenylpyridinium/toxicity , Animals , Apoptosis Inducing Factor , Caspase 2 , Caspase 3 , Caspase 6 , Caspase 7 , Caspase 8 , Caspase 9 , Cell Line , Cytochromes c/biosynthesis , Enzyme Activation , Flavoproteins/metabolism , Membrane Proteins/metabolism , Mice , Mitochondria/metabolism , Neurons/drug effects
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