Premium
Erythrocytes as targets for gamma‐glutamyltranspeptidase initiated pro‐oxidant reaction
Author(s) -
Aberkane Hayet,
Stoltz JeanFrançois,
Galteau MarieMadeleine,
Wellman Maria
Publication year - 2002
Publication title -
european journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.904
H-Index - 84
eISSN - 1600-0609
pISSN - 0902-4441
DOI - 10.1034/j.1600-0609.2002.01636.x
Subject(s) - glutathione , chemistry , red blood cell , reactive oxygen species , biochemistry , antioxidant , metabolism , enzyme , extracellular , gamma glutamyltransferase , oxidative stress , in vivo , biology , microbiology and biotechnology
Gamma‐glutamyltranspeptidase (GGT) is a well known cell plasma membrane and serum circulating enzyme. In clinical chemistry, GGT is used as a marker of alcohol consumption and drug uptake. Serum GGT activity varies in hepatobiliary diseases and cancer. This enzyme is involved in glutathione (GSH) metabolism, which is generally associated with antioxidant properties. However, in recent years, findings from our group and from others showed that GGT‐catalysed extracellular metabolism of GSH leads, in the presence of iron, to the generation of reactive oxygen species (ROS). It was demonstrated that those highly reactive species oxidise lipids, cell surface protein thiols or activate transcriptional factors such as Nuclear Factor κB (NFκB). The objective of the present work is to determine whether the red blood cells are targets for plasma GGT‐initiated pro‐oxidant reaction. The results obtained demonstrate that the GGT/GSH/iron system oxidises isolated erythrocyte membranes. A significant release of haemoglobin and a decrease of erythrocyte deformability are also observed. In addition, in vivo studies showed a relationship between plasma GGT activity and erythrocyte deformability in 20 studied subjects. In conclusion, GGT‐mediated ROS production is able to oxidise erythrocytes and thus disturbs their functions.