Prooxidant properties of p66shc are mediated by mitochondria in human cells

Autor: Alena S. Sidorenko, Evgeny R. Galimov, Boris V. Chernyak, Peter M. Chumakov, Alesya V. Tereshkova
Jazyk: angličtina
Rok vydání: 2014
Předmět:
Mitochondrial ROS
Macromolecular Assemblies
Src Homology 2 Domain-Containing
Transforming Protein 1

Gene Expression
lcsh:Medicine
Mitochondrion
Biology
Bioenergetics
medicine.disease_cause
Biosynthesis
Biochemistry
Antioxidants
Energy-Producing Processes
Cell Line
chemistry.chemical_compound
Molecular Cell Biology
medicine
Humans
Fragmentation (cell biology)
Hydrogen peroxide
lcsh:Science
Energy-Producing Organelles
chemistry.chemical_classification
Reactive oxygen species
Multidisciplinary
Cell Death
lcsh:R
Proteins
Hydrogen Peroxide
Cellular Structures
Cell biology
Enzymes
Mitochondria
Oxidative Stress
Metabolism
chemistry
Shc Signaling Adaptor Proteins
Apoptosis
Gene Knockdown Techniques
Cancer cell
lcsh:Q
Reactive Oxygen Species
Oxidation-Reduction
Oxidative stress
Research Article
Signal Transduction
Zdroj: PLoS ONE, Vol 9, Iss 3, p e86521 (2014)
PLoS ONE
ISSN: 1932-6203
Popis: p66shc is a protein product of an mRNA isoform of SHC1 gene that has a pro-oxidant and pro-apoptotic activity and is implicated in the aging process. Mitochondria were suggested as a major source of the p66shc-mediated production of reactive oxygen species (ROS), although the underlying mechanisms are poorly understood. We studied effects of p66shc on oxidative stress induced by hydrogen peroxide or by serum deprivation in human colon carcinoma cell line RKO and in diploid human dermal fibroblasts (HDFs). An shRNA-mediated knockdown of p66shc suppressed and an overexpression of a recombinant p66shc stimulated the production of ROS in the both models. This effect was not detected in the mitochondrial DNA-depleted ρ0-RKO cells that do not have the mitochondrial electron transport chain (ETC). The p66shc-dependent accumulation of mitochondrial ROS was detected with HyPer-mito, a mitochondria-targeted fluorescent protein sensor for hydrogen peroxide. The fragmentation of mitochondria induced by mitochondrial ROS was significantly reduced in the p66shc deficient RKO cells. Mitochondria-targeted antioxidants SkQ1 and SkQR1 also decreased the oxidative stress induced by hydrogen peroxide or by serum deprivation. Together the data indicate that the p66shc-dependant ROS production during oxidative stress has mitochondrial origin in human normal and cancer cells.
Databáze: OpenAIRE