Selenium‐independent epididymis‐restricted glutathione peroxidase 5 protein (GPX5) can back up failing Se‐dependent GPXs in mice subjected to selenium deficiency
Autor: | Yves Rayssiguier, Andrzej Mazur, Patrick Vernet, J. P. Dufaure, Edmond Rock, Joël R. Drevet |
---|---|
Rok vydání: | 1999 |
Předmět: |
chemistry.chemical_classification
medicine.medical_specialty Antioxidant biology GPX3 medicine.medical_treatment Glutathione peroxidase chemistry.chemical_element Cell Biology Epididymis medicine.disease GPX5 medicine.anatomical_structure Endocrinology chemistry Selenium deficiency Internal medicine Genetics biology.protein medicine Selenium Developmental Biology Peroxidase |
Zdroj: | Molecular Reproduction and Development. 54:362-370 |
ISSN: | 1098-2795 1040-452X |
DOI: | 10.1002/(sici)1098-2795(199912)54:4<362::aid-mrd6>3.0.co;2-# |
Popis: | We have previously characterized and cloned a secreted sperm-bound selenium-independent glutathione peroxidase protein (GPX5), the expression of which was found to be restricted to the mouse caput epididymidis. Because of the lack of selenium (Se) in the active site of this enzyme, unlike the other animal GPXs characterized to date, it was suspected that GPX5 does not function in the epididymis as a true glutathione peroxidase in vivo. In the present report, following dietary selenium deprivation which is known to reduce antioxidant defenses and favor oxidative stress in relation with depressed Se-dependent GPX activities, we show that the epididymis is still efficiently protected against increasing peroxidative conditions. In this model, the caput epididymides of selenium-deficient animals showed a limited production of lipid peroxides, a total GPX activity which was not dramatically affected by the shortage in selenium availability and an increase in GPX5 mRNA and protein levels. Altogether, these data strongly suggest that the selenium-independent GPX5 could function as a back-up system for Se-dependent GPXs. |
Databáze: | OpenAIRE |
Externí odkaz: |