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Variations among cultured cells in glutathione peroxidase activity in response to selenite supplementation
- Source :
- Biochimica et biophysica acta. 929(2)
- Publication Year :
- 1987
-
Abstract
- The aim of this study was to devise conditions for manipulation of the activity of selenium-dependent glutathione peroxidase in cell lines by means of variation in culture medium contents of selenite and fetal calf serum. Nine different cell lines were studied. A low glutathione peroxidase activity was, in most cases, obtained by the use of a medium with a low (2%) serum content. Selenite induced in most of the cell lines an increase in glutathione peroxidase activity, with a plateau ranging from 10 nM to 300–1000 nM. Growth-retarding effects of selenite became apparent at 300–2000 nM, showing a large cell line variation. Supplementation with 50–100 nM selenite for 1 week should generally be suitable for maximal glutathione peroxidase induction. The selenium contents of serum batches were highly variable, pointing to the importance of using only one well-defined, preferably low-selenium, batch. The glutathione peroxidase activities varied considerably between cell lines and the selenite-induced increases ranged from negligible to more than 10-fold. The availability of cell lines with such variable responses should be valuable for experiments aimed at evaluating the importance of glutathione peroxidase and selenium compounds independently of glutathione peroxidase for the protection against oxidative insult.
- Subjects :
- chemistry.chemical_classification
Fetus
Glutathione Peroxidase
Time Factors
biology
GPX3
Chemistry
Large cell
Glutathione peroxidase
chemistry.chemical_element
Cell Biology
Oxidative phosphorylation
Selenious Acid
Molecular biology
Culture Media
Selenium
Biochemistry
Cell culture
biology.protein
Humans
Enzyme inducer
Molecular Biology
Cell Division
Cells, Cultured
Subjects
Details
- ISSN :
- 00063002
- Volume :
- 929
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Biochimica et biophysica acta
- Accession number :
- edsair.doi.dedup.....c2134e5740f6dc23f06de1891498662d