Efficient transport and accumulation of vitamin C in HL-60 cells depleted of glutathione Journal Article


Authors: Guaiquil, V. H.; Farber, C. M.; Golde, D. W.; Vera, J. C.
Article Title: Efficient transport and accumulation of vitamin C in HL-60 cells depleted of glutathione
Abstract: Human myeloid leukemia cells (HL-60) transport only the oxidized form of vitamin C (dehydroascorbic acid) and accumulate the vitamin in the reduced form, ascorbic acid. We performed a detailed study of the role of glutathione in the intracellular trapping/accumulation of ascorbic acid in HL-60 cells. Uptake studies using HL-60 cells depleted of glutathione by treatment with L- buthionine-(S,R) sulfoximine and diethyl maleate, revealed no changes in the cells' ability to transport dehydroascorbic acid and accumulate ascorbic acid. Similar transport and accumulation rates were obtained using HL-60 cells containing intracellular glutathione concentrations from 6 mM to 1 μM. HL-60 cells, containing as little as 5 μM glutathione, were able to accumulate up to 150 mM ascorbic acid intracellularly when incubated with dehydroascorbic acid. Glutathione was capable of reducing dehydroascorbic acid by a direct chemical reaction, but only when present in a greater than 10-fold stoichiometric excess over dehydroascorbic acid. The accumulation of ascorbic acid by HL-60 cells was strongly temperature-dependent and was very inefficient at 16°C. On the other hand, the direct chemical reduction of dehydroascorbic acid by excess glutathione proceeded efficiently at temperatures of 16°C. Our data indicate that glutathione-dependent reductases in HL-60 cells are not responsible for the ability of these cells to accumulate millimolar concentrations of ascorbic acid. These findings indicate that alternative enzymatic mechanisms are involved in the cellular reduction of dehydroascorbic acid.
Keywords: human cell; intracellular transport; temperature; ascorbic acid; cell level; temperature sensitivity; dehydroascorbic acid; biological transport; glutathione; antimetabolites; hl-60 cells; vitamin metabolism; humans; human; priority journal; article; buthionine sulfoximine; maleates
Journal Title: Journal of Biological Chemistry
Volume: 272
Issue: 15
ISSN: 0021-9258
Publisher: American Society for Biochemistry and Molecular Biology  
Date Published: 1997-04-11
Start Page: 9915
End Page: 9921
Language: English
DOI: 10.1074/jbc.272.15.9915
PUBMED: 9092530
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 17 March 2017 -- Source: Scopus
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  1. Juan C Vera
    64 Vera
  2. David Golde
    127 Golde