Vitamin C and immune cell function in inflammation and cancer

被引:128
作者
Ang, Abel [1 ]
Pullar, Juliet M. [2 ]
Currie, Margaret J. [1 ]
Vissers, Margreet C. M. [2 ]
机构
[1] Univ Otago, Dept Pathol & Biomed Sci, Mackenzie Canc Res Grp, Christchurch 8011, New Zealand
[2] Univ Otago, Dept Pathol & Biomed Sci, Ctr Free Rad Res, Christchurch 8011, New Zealand
关键词
HYPOXIA-INDUCIBLE FACTOR; REGULATORY T-CELLS; CYTOKINE GENE-EXPRESSION; ASCORBIC-ACID; NEUTROPHIL APOPTOSIS; DNA DEMETHYLATION; DENDRITIC CELLS; IN-VIVO; MACROPHAGE POLARIZATION; HYPOVITAMINOSIS-C;
D O I
10.1042/BST20180169
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vitamin C (ascorbate) is maintained at high levels in most immune cells and can affect many aspects of the immune response. Intracellular levels generally respond to variations in plasma ascorbate availability, and a combination of inadequate intake and increased turnover during severe stress can result in low plasma ascorbate status. Intracellular ascorbate supports essential functions and, in particular, acts as an enzyme cofactor for Fe-or Cu-containing oxygenases. Newly discovered enzymes in this family regulate cell metabolism and epigenetics, and dysregulation of their activity can affect cell phenotype, growth and survival pathways, and stem cell phenotype. This brief overview details some of the recent advances in our understanding of how ascorbate availability can affect the hydroxylases controlling the hypoxic response and the DNA and histone demethylases. These processes play important roles in the regulation of the immune system, altering cell survival pathways, metabolism and functions.
引用
收藏
页码:1147 / 1159
页数:13
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