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Mitochondria, calcium-dependent neuronal death and neurodegenerative disease
Understanding the mechanisms of neuronal dysfunction and death represents a major frontier in contemporary medicine, involving the acute cell death in stroke, and the attrition of the major neurodegenerative diseases, including Parkinson's, Alzheimer's, Huntington's and Motoneuron dis...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer-Verlag
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3387496/ https://www.ncbi.nlm.nih.gov/pubmed/22615071 http://dx.doi.org/10.1007/s00424-012-1112-0 |
Sumario: | Understanding the mechanisms of neuronal dysfunction and death represents a major frontier in contemporary medicine, involving the acute cell death in stroke, and the attrition of the major neurodegenerative diseases, including Parkinson's, Alzheimer's, Huntington's and Motoneuron diseases. A growing body of evidence implicates mitochondrial dysfunction as a key step in the pathogenesis of all these diseases, with the promise that mitochondrial processes represent valuable potential therapeutic targets. Each disease is characterised by the loss of a specific vulnerable population of cells—dopaminergic neurons in Parkinson's disease, spinal motoneurons in Motoneuron disease, for example. We discuss the possible roles of cell type-specific calcium signalling mechanisms in defining the pathological phenotype of each of these major diseases and review central mechanisms of calcium-dependent mitochondrial-mediated cell death. |
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