Vitamin C and immune cell function in inflammation and cancer
Author(s) -
Abel Damien Ang,
Juliet M. Pullar,
Margaret J. Currie,
Margreet C.M. Vissers
Publication year - 2018
Publication title -
biochemical society transactions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.562
H-Index - 144
eISSN - 1470-8752
pISSN - 0300-5127
DOI - 10.1042/bst20180169
Subject(s) - immune system , epigenetics , intracellular , biology , phenotype , microbiology and biotechnology , cell metabolism , inflammation , cell , cell growth , plasma cell , enzyme , metabolism , biochemistry , immunology , antibody , gene
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.
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