G6PD deficient cells and the bioreduction of disulfides: Effects of DHEA, GSH depletion and phenylarsine oxide

Citation
Je. Biaglow et al., G6PD deficient cells and the bioreduction of disulfides: Effects of DHEA, GSH depletion and phenylarsine oxide, BIOC BIOP R, 273(3), 2000, pp. 846-852
Citations number
36
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
ISSN journal
0006291X → ACNP
Volume
273
Issue
3
Year of publication
2000
Pages
846 - 852
Database
ISI
SICI code
0006-291X(20000714)273:3<846:GDCATB>2.0.ZU;2-V
Abstract
We used Glucose 6 phosphate dehydrogenase (G6PD) minus cells (89 cells) and G6PD containing cells (KI) to understand the mechanisms of bioreduction of disulfide and the redox regulation of protein and non protein thiols in ma mmalian cells. The 89 cells reduce hydroxyethyldisulfide (HEDS) to mercapto ethanol (ME) at a slower rate than K1 cells. HEDS reduction results in loss of nonprotein thiols (NPSH) and a decrease in protein thiols (PSH) in 89 c ells. The effects are less dramatic with K1 cells, However, the loss of NPS H and PSH in K1 cells are increased in the absence of glucose. Glutathione- depletion with L-BSO partially blocks HEDS reduction in K1 and 89 cells. Tr eatment with the vicinal thiol reagent phenyl arsenic oxide (PAO) blocks re duction of HEDS in both cells. Surprisingly, dehydroepiandrosterone (DHEA), a known inhibitor of G6PD, inhibits the growth and blocks the reduction of HEDS both in 89 and K1 cells suggesting that its mechanism for inhibition of growth is not G6PD related. (C) 2000 academic Press.