TY - JOUR
T1 - Vitamin C is an essential antioxidant that enhances survival of oxidatively stressed human vascular endothelial cells in the presence of a vast molar excess of glutathione
AU - Montecinos, Viviana
AU - Guzmán, Paula
AU - Barra, Valeria
AU - Villagrán, Marcelo
AU - Muñoz-Montesino, Carola
AU - Sotomayor, Kirsty
AU - Escobar, Elizabeth
AU - Godoy, Alejandro
AU - Mardones, Lorena
AU - Sotomayor, Paula
AU - Guzmán, Catherine
AU - Vásquez, Osmán
AU - Gallardo, Victoria
AU - Van Zundert, Brigitte
AU - Bono, María Rosa
AU - Oñate, Sergio A.
AU - Bustamante, Marcelo
AU - Cárcamo, Juan G.
AU - Rivas, Coralia I.
AU - Vera, Juan Carlos
PY - 2007/5/25
Y1 - 2007/5/25
N2 - Cellular glutathione levels may exceed vitamin C levels by 10-fold, generating the question about the real antioxidant role that low intracellular concentrations of vitamin C can play in the presence of a vast molar excess of glutathione. We characterized the metabolism of vitamin C and its relationship with glutathione in primary cultures of human endothelial cells oxidatively challenged by treatment with hydrogen peroxide or with activated cells undergoing the respiratory burst, and analyzed the manner in which vitamin C interacts with glutathione to increase the antioxidant capacity of cells. Our data indicate that: (i) endothelial cells express transporters for reduced and oxidized vitamin C and accumulate ascorbic acid with participation of glutathione-dependent dehydroascorbic acid reductases, (ii) although increased intracellular levels of vitamin C or glutathione caused augmented resistance to oxidative stress, 10-times more glutathione than vitamin C was required, (iii) full antioxidant protection required the simultaneous presence of intracellular and extracellular vitamin C at concentrations normally found in vivo, and (iv) intracellular vitamin C cooperated in enhancing glutathione recovery after oxidative challenge thus providing cells with enhanced survival potential, while extracellular vitamin C was recycled through a mechanism involving the simultaneous neutralization of oxidant species. Therefore, in endothelial cells under oxidative challenge, vitamin C functions as an essential cellular antioxidant even in the presence of a vast molar excess of glutathione.
AB - Cellular glutathione levels may exceed vitamin C levels by 10-fold, generating the question about the real antioxidant role that low intracellular concentrations of vitamin C can play in the presence of a vast molar excess of glutathione. We characterized the metabolism of vitamin C and its relationship with glutathione in primary cultures of human endothelial cells oxidatively challenged by treatment with hydrogen peroxide or with activated cells undergoing the respiratory burst, and analyzed the manner in which vitamin C interacts with glutathione to increase the antioxidant capacity of cells. Our data indicate that: (i) endothelial cells express transporters for reduced and oxidized vitamin C and accumulate ascorbic acid with participation of glutathione-dependent dehydroascorbic acid reductases, (ii) although increased intracellular levels of vitamin C or glutathione caused augmented resistance to oxidative stress, 10-times more glutathione than vitamin C was required, (iii) full antioxidant protection required the simultaneous presence of intracellular and extracellular vitamin C at concentrations normally found in vivo, and (iv) intracellular vitamin C cooperated in enhancing glutathione recovery after oxidative challenge thus providing cells with enhanced survival potential, while extracellular vitamin C was recycled through a mechanism involving the simultaneous neutralization of oxidant species. Therefore, in endothelial cells under oxidative challenge, vitamin C functions as an essential cellular antioxidant even in the presence of a vast molar excess of glutathione.
UR - http://www.scopus.com/inward/record.url?scp=34447505075&partnerID=8YFLogxK
U2 - 10.1074/jbc.M608361200
DO - 10.1074/jbc.M608361200
M3 - Article
C2 - 17403685
AN - SCOPUS:34447505075
SN - 0021-9258
VL - 282
SP - 15506
EP - 15515
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 21
ER -