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Nat Cell Biol ; 1(3): 152-7, 1999 Jul.
Article in English | MEDLINE | ID: mdl-10559901

ABSTRACT

Haem oxygenase-1 (HO1) is a heat-shock protein that is induced by stressful stimuli. Here we demonstrate a cytoprotective role for HO1: cell death produced by serum deprivation, staurosporine or etoposide is markedly accentuated in cells from mice with a targeted deletion of the HO1 gene, and greatly reduced in cells that overexpress HO1. Iron efflux from cells is augmented by HO1 transfection and reduced in HO1-deficient fibroblasts. Iron accumulation in HO1-deficient cells explains their death: iron chelators protect HO1-deficient fibroblasts from cell death. Thus, cytoprotection by HO1 is attributable to its augmentation of iron efflux, reflecting a role for HO1 in modulating intracellular iron levels and regulating cell viability.


Subject(s)
Apoptosis/physiology , Heme Oxygenase (Decyclizing)/genetics , Heme Oxygenase (Decyclizing)/metabolism , Iron/metabolism , Skin/metabolism , Animals , Apoptosis/drug effects , Apoptosis/genetics , Cell Line , Cell Survival/drug effects , Cell Survival/physiology , Cells, Cultured , Cloning, Molecular , Culture Media, Serum-Free , Etoposide/pharmacology , Fibroblasts/cytology , Fibroblasts/metabolism , Fibroblasts/pathology , Gene Deletion , Heme Oxygenase (Decyclizing)/deficiency , Heme Oxygenase-1 , Humans , Membrane Proteins , Mice , Mice, Knockout , Recombinant Proteins/metabolism , Skin/cytology , Skin/drug effects , Staurosporine/pharmacology , Transfection
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