Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9002142 | Biochemical Pharmacology | 2005 | 12 Pages |
Abstract
Exposure to an otherwise non-toxic concentration of peroxynitrite (ONOOâ) promotes toxicity in U937 cells supplemented with pharmacological inhibitors of protein kinase C (PKC). This effect is not associated with enhanced formation of H2O2 and is in fact causally linked to inhibition of the cytoprotective signalling driven by endogenous arachidonic acid (AA). The outcome of various approaches using PKC or phospholipase A2 inhibitors, cytosolic phospholipase A2 or PKCα antisense-oligonucleotide-transfected cells and supplementation with exogenous AA or tetradecanoylphorbol acetate, as well as PKC down-regulated cells, indicated that ONOOâ promotes AA-dependent cytosol to membrane translocation of PKCα, an event critical for the cytoprotective signalling under investigation. Evidence for a similar mechanism regulating survival of human monocytes exposed to ONOOâ is also presented. These results, along with our previous work on this topic, contribute to the definition of the mechanism whereby monocytes survive to ONOOâ in inflamed tissues.
Keywords
AACOCF3ETYAPLA2DHRCalcein-AMPKCTetradecanoylphorbol acetatecPLA2MPTarachidonyl trifluoromethyl ketonetPAphospholipase A25,8,11,14-eicosatetraynoic acidArachidonic acidmitochondrial permeability transitionCSAdihydrorhodamine 123Toxicologycyclosporin Acytosolic phospholipase A2Cell deathProtein kinase CαProtein kinase CPeroxynitritecalcein acetoxymethyl ester
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Authors
Andrea Guidarelli, Liana Cerioni, Ilaria Tommasini, Bernhard Brüne, Orazio Cantoni,