Literature DB >> 2009284

Ascorbate is regenerated by HL-60 cells through the transplasmalemma redox system.

F J Alcain1, M I Buron, J M Villalba, P Navas.   

Abstract

Ascorbate was maintained in the media during a long-term culture by HL-60 cells. The chemical oxidation of ascorbate was reversed in vitro by living HL-60 cells and was related to the amount of cells added. The increase of NADH concentration by lactate addition to cells was accompanied by an increase of both ascorbate regeneration and ferricyanide reduction. Further, plasma membrane enriched fractions from HL-60 cells revealed enhancement of both ascorbate regeneration and ferricyanide reduction in the presence of NADH when previously treated with detergent. The blockage of cell surface carbohydrates by wheat germ agglutinin (WGA) and Concanavalina ensiformis (Con A) lectins significantly inhibited the regeneration of ascorbate caused by the cells. These results support the idea that ascorbate is externally regenerated by the NADH-ascorbate free radical reductase as a part of the transplasma membrane redox system.

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Year:  1991        PMID: 2009284     DOI: 10.1016/0304-4165(91)90146-8

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  16 in total

1.  Role of ascorbate in the activation of NF-kappaB by tumour necrosis factor-alpha in T-cells.

Authors:  E Muñoz; M V Blázquez; C Ortiz; C Gomez-Díaz; P Navas
Journal:  Biochem J       Date:  1997-07-01       Impact factor: 3.857

2.  Interaction of respiratory burst and uptake of dehydroascorbic acid in differentiated HL-60 cells.

Authors:  H Laggner; H Goldenberg
Journal:  Biochem J       Date:  2000-01-15       Impact factor: 3.857

3.  Antioxidant ascorbate is stabilized by NADH-coenzyme Q10 reductase in the plasma membrane.

Authors:  C Gómez-Díaz; J C Rodríguez-Aguilera; M P Barroso; J M Villalba; F Navarro; F L Crane; P Navas
Journal:  J Bioenerg Biomembr       Date:  1997-06       Impact factor: 2.945

4.  Plasma membrane ubiquinone controls ceramide production and prevents cell death induced by serum withdrawal.

Authors:  M P Barroso; C Gómez-Díaz; J M Villalba; M I Burón; G López-Lluch; P Navas
Journal:  J Bioenerg Biomembr       Date:  1997-06       Impact factor: 2.945

5.  NADH-ascorbate free radical and -ferricyanide reductase activities represent different levels of plasma membrane electron transport.

Authors:  J M Villalba; A Canalejo; J C Rodríguez-Aguilera; M I Burón; D J Mooré; P Navas
Journal:  J Bioenerg Biomembr       Date:  1993-08       Impact factor: 2.945

6.  Extracellular ascorbate stabilization as a result of transplasma electron transfer in Saccharomyces cerevisiae.

Authors:  C Santos-Ocaña; P Navas; F L Crane; F Córdoba
Journal:  J Bioenerg Biomembr       Date:  1995-12       Impact factor: 2.945

7.  Efflux of hepatic ascorbate: a potential contributor to the maintenance of plasma vitamin C.

Authors:  J M Upston; A Karjalainen; F L Bygrave; R Stocker
Journal:  Biochem J       Date:  1999-08-15       Impact factor: 3.857

8.  Mouse liver plasma membrane redox system activity is altered by aging and modulated by calorie restriction.

Authors:  G López-Lluch; M Rios; M A Lane; P Navas; R de Cabo
Journal:  Age (Dordr)       Date:  2005-12-10

9.  Response to adriamycin of transplasma membrane electron transport in adriamycin-resistant and nonresistant HL-60 cells.

Authors:  D J Morré; D M Morré; L Y Wu
Journal:  J Bioenerg Biomembr       Date:  1994-02       Impact factor: 2.945

Review 10.  Ascorbate and plant cell growth.

Authors:  F Córdoba; J A González-Reyes
Journal:  J Bioenerg Biomembr       Date:  1994-08       Impact factor: 2.945

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