TY - JOUR
T1 - Inverse correlation between resistance towards copper and towards the redox-cycling compound paraquat
T2 - A study in copper-tolerant hepatocytes in tissue culture
AU - Zer, Hagit
AU - Freedman, Jonathan H.
AU - Peisach, Jack
AU - Chevion, Mordechai
PY - 1991
Y1 - 1991
N2 - The essential mediatory role of copper or iron in the manifestation of paraquat toxicity has been demonstrated (Kohen and Chevion (1985) Free Rad. Res. Commun. 1, 79-88; Korbashi, P. et al. (1986) J. Biol. Chem. 261, 12472-12476). Several liver cell lines, characterized by their resistance to copper, were challenged with paraquat and their cross-resistance to paraquat and copper was studied. Cell growth and survival data showed that copper-resistant cells, containing elevated copper, are more sensitive towards paraquat than wild type cells. Copper-deprived resistant cells did not have this sensitivity. Paraquat was also shown to cause a marked degradation of cellular glutathione in all cell lines. Albeit the fact that the basal glutathione levels are higher in copper-resistant than in wild type cells, there is more paraquat-induced degradation of cellular glutathione (GSH + GSSG) in resistant cells. It is suggested that in copper-resistant cells which contain elevated levels of copper, paraquat-induced cellular injury is potentiated even where glutathione levels are elevated. Additionally, in vitro experiments are presented that support the in vivo findings demonstrating a role for copper in glutathione degradation.
AB - The essential mediatory role of copper or iron in the manifestation of paraquat toxicity has been demonstrated (Kohen and Chevion (1985) Free Rad. Res. Commun. 1, 79-88; Korbashi, P. et al. (1986) J. Biol. Chem. 261, 12472-12476). Several liver cell lines, characterized by their resistance to copper, were challenged with paraquat and their cross-resistance to paraquat and copper was studied. Cell growth and survival data showed that copper-resistant cells, containing elevated copper, are more sensitive towards paraquat than wild type cells. Copper-deprived resistant cells did not have this sensitivity. Paraquat was also shown to cause a marked degradation of cellular glutathione in all cell lines. Albeit the fact that the basal glutathione levels are higher in copper-resistant than in wild type cells, there is more paraquat-induced degradation of cellular glutathione (GSH + GSSG) in resistant cells. It is suggested that in copper-resistant cells which contain elevated levels of copper, paraquat-induced cellular injury is potentiated even where glutathione levels are elevated. Additionally, in vitro experiments are presented that support the in vivo findings demonstrating a role for copper in glutathione degradation.
KW - Copper
KW - Copper resistance
KW - Glutathione
KW - Hepatoma cells
KW - Paraquat
UR - http://www.scopus.com/inward/record.url?scp=0025772685&partnerID=8YFLogxK
U2 - 10.1016/0891-5849(91)90182-3
DO - 10.1016/0891-5849(91)90182-3
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 1937132
AN - SCOPUS:0025772685
SN - 0891-5849
VL - 11
SP - 9
EP - 16
JO - Free Radical Biology and Medicine
JF - Free Radical Biology and Medicine
IS - 1
ER -