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Flavonoid-rich berry-extract influences expression of genes in the iron-uptake pathway in human intestinal Caco-2 cells

Published online by Cambridge University Press:  19 November 2010

F. Alzaid ,
K. Pourvali ,
G. Sekhon ,
P. A. Sharp ,
V. R. Preedy  and
H. Wiseman
F. Alzaid
Affiliation:
King's College London, Nutritional Sciences Division, Franklin-Wilkins Building, 150 Stamford Street, London SE1 9NH,UK
K. Pourvali
Affiliation:
King's College London, Nutritional Sciences Division, Franklin-Wilkins Building, 150 Stamford Street, London SE1 9NH,UK
G. Sekhon
Affiliation:
King's College London, Nutritional Sciences Division, Franklin-Wilkins Building, 150 Stamford Street, London SE1 9NH,UK
P. A. Sharp
Affiliation:
King's College London, Nutritional Sciences Division, Franklin-Wilkins Building, 150 Stamford Street, London SE1 9NH,UK
V. R. Preedy
Affiliation:
King's College London, Nutritional Sciences Division, Franklin-Wilkins Building, 150 Stamford Street, London SE1 9NH,UK
H. Wiseman
Affiliation:
King's College London, Nutritional Sciences Division, Franklin-Wilkins Building, 150 Stamford Street, London SE1 9NH,UK
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Abstract

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Proceedings of the Nutrition Society , Volume 69 , Issue OCE6: Summer Meeting, 28 June–1 July 2010, Nutrition and health: cell to community , 2010 , E464
Copyright
Copyright © The Authors 2010

Berries are a rich dietary source of bioactive polyphenols, including flavonoids, such as anthocyanins(Reference Zafra-Stone, Yasmin and Bagchi1). Dietary flavonoids are known to impair Fe absorption and reduce non-haem-Fe transport across Caco-2 cell monolayers(Reference Kim, Ham and Shigenaga2). Previously, we demonstrated that a flavonoid-rich berry-extract decreases the expression of the divalent metal ion transporter (DMT1) and the haemochromatosis (HFE) genes, involved in the Fe-uptake pathway(Reference Alzaid, Pourvali and Lin3). The present study investigated the influence of this berry-extract on the gene expression and corresponding protein abundance of the apical ferrireductase, duodenal cytochrome B (DCYTB), the basolateral Fe efflux protein, ferroportin (FPN), the basolateral ferroxidase, hephaestin (HEPH) and DMT1 and HFE, which co-ordinate intestinal Fe transport(Reference Garrick, Dolan and Horbinski4).

Human intestinal Caco-2 cells, cultured for 21 d, were then treated for 16 h with an anthocyanin-rich berry-extract (OptiBerry; InterHealth Nutraceuticals, Benicia, CA, USA) at a final concentration of 0.5% (w/v). RNA and protein were isolated for quantitative RT–PCR and western blotting, respectively. All gene expression data were normalised to 18S and GAPDH as housekeeping genes and presented as mean normalised expression ratio and sem. All protein quantity data were normalised per μg of protein and presented as mean integral/¶g protein and sem. Statistical significance was determined by Student's unpaired t-test with significance indicated at P⩽0.05.

Following treatment with the berry-extract, there were significant decreases in DMT1 (mean 0.63 (sem 0.07), p⩽0.039, n 6) and HFE (mean 0.52 (sem 0.05), P⩽0.0001, n 6) mRNA expression. The abundance of the proteins HEPH and FPN, involved in the basolateral release of Fe, was significantly increased (Fig. 1).

These results indicate that berry-flavonoids influence the expression of components of the Fe-uptake pathway. Studies are in progress to investigate the biological relevance of the observed effects in relation to berry consumption and the bioavailability of dietary Fe.

References

1.Zafra-Stone, S, Yasmin, T, Bagchi, M et al. (2007) Berry anthocyanins as novel antioxidants in human health and disease prevention. Mol Nutr Food Res. 51, 675–683.CrossRefGoogle ScholarPubMed
2.Kim, EY, Ham, SK, Shigenaga, MK et al. (2008) Bioactive dietary polyphenolic compounds reduce nonheme iron transport across human intestinal cell monolayers. J Nutr. 138, 1647–1651.CrossRefGoogle ScholarPubMed
3.Alzaid, F, Pourvali, K, Lin, CI et al. (2010) Flavonoid-rich-berry-extract treatment decreases the expression of DMT1 and functionally-similar metal transporter genes in human intestinal Caco-2 cells.Proc Nutr Soc. 69, (OCE1), E27.Google Scholar
4.Garrick, MD, Dolan, KG, Horbinski, C et al. (2003) DMT1: a mammalian transporter for multiple metals. Biometals 16, 41–1654.CrossRefGoogle ScholarPubMed