In vivo vitamin C supplementation increases phosphoinositol transfer protein expression in peripheral blood mononuclear cells from healthy individuals

Ascorbate can act as both a reducing and oxidising agent in vitro depending on its environment. It can modulate the intracellular redox environment of cells and therefore is predicted to modulate thiol-dependent cell signalling and gene expression pathways. Using proteomic analysis of vitamin C-trea...

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Published inBritish journal of nutrition Vol. 101; no. 10; pp. 1432 - 1437
Main Authors Griffiths, Helen R, Willetts, Rachel S, Grant, Melissa M, Mistry, Nalini, Lunec, Joe, Bevan, Ruth J
Format Journal Article
LanguageEnglish
Published Cambridge, UK Cambridge University Press 28.05.2009
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Summary:Ascorbate can act as both a reducing and oxidising agent in vitro depending on its environment. It can modulate the intracellular redox environment of cells and therefore is predicted to modulate thiol-dependent cell signalling and gene expression pathways. Using proteomic analysis of vitamin C-treated T cells in vitro, we have previously reported changes in expression of five functional protein groups associated with signalling, carbohydrate metabolism, apoptosis, transcription and immune function. The increased expression of the signalling molecule phosphatidylinositol transfer protein (PITP) was also confirmed using Western blotting. Herein, we have compared protein changes elicited by ascorbate in vitro, with the effect of ascorbate on plasma potassium levels, on peripheral blood mononuclear cell (PBMC) apoptosis and PITP expression, in patients supplemented with vitamin C (0-2 g/d) for up to 10 weeks to investigate whether in vitro model systems are predictive of in vivo effects. PITP varied in expression widely between subjects at all time-points analysed but was increased by supplementation with 2 g ascorbate/d after 5 and 10 weeks. No effects on plasma potassium levels were observed in supplemented subjects despite a reduction of K+ channel proteins in ascorbate-treated T cells in vitro. Similarly, no effect of vitamin C supplementation on PBMC apoptosis was observed, whilst ascorbate decreased expression of caspase 3 recruitment domain protein in vitro. These data provide one of the first demonstrations that proteomics may be valuable in developing predictive markers of nutrient effects in vivo and may identify novel pathways for studying mechanisms of action in vivo.
Bibliography:http://dx.doi.org/10.1017/S0007114508079646
PII:S0007114508079646
ArticleID:07964
Abbreviations: PITP, phosphoinositol transfer protein; PBMC, peripheral blood mononuclear cell; Tris, 2-amino-2-hydroxymethyl-1,3-propanediol; TTBS, Tween Tris-buffered saline
istex:A86ED6D748668F8815DE939D52184624FCA07D4D
Present address: Birmingham University Dental School, UK.
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ISSN:0007-1145
1475-2662
1475-2662
DOI:10.1017/S0007114508079646