Minor thiols cysteine and cysteinylglycine regulate the competition between glutathione and protein SH groups in human platelets subjected to oxidative stress

Arch Biochem Biophys. 2000 Aug 1;380(1):1-10. doi: 10.1006/abbi.2000.1847.

Abstract

Changes in the concentrations of protein-mixed disulfides (XS-SP) of glutathione (GSH), cysteine (CSH), and cysteinylglycine (CGSH) were studied in human platelets treated with diamide and t-BOOH in timecourse experiments (time range, 1-30 min) in order to understand the contribution of minor thiols CSH and CGSH to the regulation of glutathione-protein mixed disulfides (GS-SP). Diamide was much more potent than t-BOOH in altering the platelet thiol composition of XS-SP (threshold dose: diamide, 0.03 mM; t-BOOH, 0.5 mM) and caused reversible XS-SP peaks whose magnitude was related to the concentration of free thiols in untreated cells. Thus maximum levels of GS-SP (8 min after 0.4 mM diamide) were about 16-fold higher than those of controls (untreated platelets, GS-SP = 0.374 nmol/10(9) platelets), whereas those of CS-SP and CGS-SP were only 4-fold increased (untreated platelets, CS-SP = 0.112 nmol/10(9) platelets; CGS-SP = 0.024 nmol/10(9) platelets). The greater effects of diamide with respect to t-BOOH were explained on the basis of the activities of fast reactive protein SH groups for diamide and glutathione reductase (GR) and glucose-6-phosphate dehydrogenase (G-6-PDH) for t-BOOH. The addition of cysteine (0.3 mM, at 4 min) after treatment of platelets with 0.4 mM diamide increased the rate of reversal of GS-SP peaks to normal values, but also caused a relevant change in CGS-SP with respect to that of platelets treated with diamide alone. An increased gamma-glutamyltranspeptidase activity was found in platelets treated with diamide. Moreover, untreated platelets were found to release and hydrolyze GSH to CGSH and CSH. Ratios of thiols/disulfides (XSH/XSSX) and activities of GR and G-6PDH were also related to a high reducing potential exerted by GSH but not by minor thiols. The lower mass and charge of minor thiols is a likely requisite of the regulation of GS-SP levels in platelets.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antioxidants / metabolism
  • Blood Platelets / drug effects*
  • Blood Platelets / metabolism*
  • Chromatography, High Pressure Liquid
  • Cysteine / metabolism*
  • Diamide / pharmacology
  • Dipeptides / metabolism*
  • Disulfides / metabolism
  • Dithionitrobenzoic Acid / pharmacology
  • Erythrocytes / metabolism
  • Glutathione / metabolism*
  • Humans
  • Oxidative Stress
  • Spectrophotometry
  • Sulfhydryl Compounds / physiology*
  • Time Factors
  • src Homology Domains*
  • tert-Butylhydroperoxide / pharmacology

Substances

  • Antioxidants
  • Dipeptides
  • Disulfides
  • Sulfhydryl Compounds
  • Diamide
  • cysteinylglycine
  • tert-Butylhydroperoxide
  • Dithionitrobenzoic Acid
  • Glutathione
  • Cysteine