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Antioxidant activity is required for the protective effects of cyclophilin A against oxidative stress.
- Source :
-
Molecular medicine reports [Mol Med Rep] 2015 Jul; Vol. 12 (1), pp. 712-8. Date of Electronic Publication: 2015 Feb 26. - Publication Year :
- 2015
-
Abstract
- Cyclophilin (Cyp) belongs to a group of proteins that have peptidyl-prolyl cis-trans isomerase (PPIase) activity. CypA is the major cellular target for the immunosuppressive drug cyclosporin A and mediates its actions. Previous studies have demonstrated that CypA has diverse cellular functions and have suggested that CypA may function as an antioxidant. The present study investigated the antioxidant activity of CypA and its association with PPIase activity. The purified CypA/wild-type (WT) and CypA/P16S mutant proteins were active in PPIase assays. A total antioxidant capacity assay revealed that the purified CypA/WT protein had significantly higher antioxidant activity, whereas the CypA/P16S mutant was defective in its antioxidant activity. To confirm the importance of CypA antioxidant activity, CypA/P16S was overexpressed in Chang human liver cells and the rate of cell death was measured following treatment with cisplatin or H2O2. Overexpression of CypA/WT protected the cells against cisplatin or H2O2-induced oxidative damage, however, the CypA/P16S mutant had no effect. These findings suggested that CypA exhibits a protective antioxidant effect.
- Subjects :
- Cisplatin administration & dosage
Cyclophilin A genetics
Gene Expression Regulation drug effects
Humans
Hydrogen Peroxide administration & dosage
Immunosuppressive Agents administration & dosage
Liver cytology
Liver metabolism
Organic Anion Transporters biosynthesis
Organic Anion Transporters genetics
Oxidative Stress drug effects
Peptidylprolyl Isomerase genetics
Reactive Oxygen Species metabolism
Recombinant Fusion Proteins biosynthesis
Recombinant Fusion Proteins genetics
Antioxidants administration & dosage
Cyclophilin A biosynthesis
Oxidative Stress genetics
Peptidylprolyl Isomerase biosynthesis
Subjects
Details
- Language :
- English
- ISSN :
- 1791-3004
- Volume :
- 12
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Molecular medicine reports
- Publication Type :
- Academic Journal
- Accession number :
- 25738284
- Full Text :
- https://doi.org/10.3892/mmr.2015.3392