Journal of Alzheimer's Disease
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Home > Caspase signalling controls microglia activation and neurotoxicity.

TitleCaspase signalling controls microglia activation and neurotoxicity.
Publication TypeJournal Article
Year of Publication2011
AuthorsBurguillos, MA, Deierborg, T, Kavanagh, E, Persson, A, Hajji, N, Garcia-Quintanilla, A, Cano, J, Brundin, P, Englund, E, Venero, JL, Joseph, B
JournalNature
Volume472
Issue7343
Pagination319-24
Date Published2011 Apr 21
ISSN1476-4687
KeywordsAlzheimer Disease, Animals, Caspase 3, Caspase 7, Caspase 8, Caspase Inhibitors, Caspases, Cell Death, Cells, Cultured, Dopamine, Enzyme Activation, Frontal Lobe, Gene Knockdown Techniques, Humans, Lipopolysaccharides, Mice, Microglia, Neostriatum, Neurotoxicity Syndromes, Parkinson Disease, Protein Kinase C-delta, Rats, Signal Transduction, Substantia Nigra, Toll-Like Receptor 4
Abstract

Activation of microglia and inflammation-mediated neurotoxicity are suggested to play a decisive role in the pathogenesis of several neurodegenerative disorders. Activated microglia release pro-inflammatory factors that may be neurotoxic. Here we show that the orderly activation of caspase-8 and caspase-3/7, known executioners of apoptotic cell death, regulate microglia activation through a protein kinase C (PKC)-δ-dependent pathway. We find that stimulation of microglia with various inflammogens activates caspase-8 and caspase-3/7 in microglia without triggering cell death in vitro and in vivo. Knockdown or chemical inhibition of each of these caspases hindered microglia activation and consequently reduced neurotoxicity. We observe that these caspases are activated in microglia in the ventral mesencephalon of Parkinson's disease (PD) and the frontal cortex of individuals with Alzheimer's disease (AD). Taken together, we show that caspase-8 and caspase-3/7 are involved in regulating microglia activation. We conclude that inhibition of these caspases could be neuroprotective by targeting the microglia rather than the neurons themselves.

DOI10.1038/nature09788
Alternate JournalNature
PubMed ID21389984
Top50 Topics: 
Physiology, Pathology
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