Selenium Discrepancies in Fetal Bovine Serum: Impact on Cellular Selenoprotein Expression.
GPX1
GPX4
TXNRD1
selenium concentration
selenocysteine
selenoprotein
triple quadrupole ICP-MS
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
01 Jul 2024
01 Jul 2024
Historique:
received:
30
04
2024
revised:
19
06
2024
accepted:
27
06
2024
medline:
13
7
2024
pubmed:
13
7
2024
entrez:
13
7
2024
Statut:
epublish
Résumé
Selenium is an essential trace element in our diet, crucial for the composition of human selenoproteins, which include 25 genes such as glutathione peroxidases and thioredoxin reductases. The regulation of the selenoproteome primarily hinges on the bioavailability of selenium, either from dietary sources or cell culture media. This selenium-dependent control follows a specific hierarchy, with "housekeeping" selenoproteins maintaining constant expression while "stress-regulated" counterparts respond to selenium level fluctuations. This study investigates the variability in fetal bovine serum (FBS) selenium concentrations among commercial batches and its effects on the expression of specific stress-related cellular selenoproteins. Despite the limitations of our study, which exclusively used HEK293 cells and focused on a subset of selenoproteins, our findings highlight the substantial impact of serum selenium levels on selenoprotein expression, particularly for GPX1 and GPX4. The luciferase reporter assay emerged as a sensitive and precise method for evaluating selenium levels in cell culture environments. While not exhaustive, this analysis provides valuable insights into selenium-mediated selenoprotein regulation, emphasizing the importance of serum composition in cellular responses and offering guidance for researchers in the selenoprotein field.
Identifiants
pubmed: 39000368
pii: ijms25137261
doi: 10.3390/ijms25137261
pii:
doi:
Substances chimiques
Selenium
H6241UJ22B
Selenoproteins
0
Glutathione Peroxidase
EC 1.11.1.9
Glutathione Peroxidase GPX1
EC 1.11.1.9
Phospholipid Hydroperoxide Glutathione Peroxidase
EC 1.11.1.12
Culture Media
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : French National Centre for Scientific Research
ID : dotation
Organisme : Inserm
ID : dotation
Organisme : ENS de Lyon
ID : dotation
Organisme : Agence Nationale de Recherches sur le Sida et les Hépatites Virales
ID : research grant