Ascorbic Acid Promotes Plasma Cell Differentiation through Enhancing TET2/3-Mediated DNA Demethylation

Cell Rep. 2020 Dec 1;33(9):108452. doi: 10.1016/j.celrep.2020.108452.

Abstract

Plasma cells provide high-affinity antibodies against invading pathogens. Although transcriptional and epigenetic mechanisms have been extensively studied for plasma cell differentiation, how these mechanisms respond to environmental cues remains largely unexplored. In this study, we show that ascorbic acid (vitamin C), an essential nutrient, is able to promote plasma cell differentiation and humoral immune response by enhancing TET2/3-mediated DNA demethylation. Ascorbic acid treatment during B cell activation has persistent effects on later plasma cell differentiation by predisposing germinal center B cells toward the plasma cell lineage. Conversely, ascorbic acid deficiency in vivo blocks plasma cell differentiation and attenuates the humoral immune response following antigen immunization. We further demonstrate that such effects of ascorbic acid on plasma cell differentiation require DNA methylcytosine oxidases TET2 and TET3. Our study thus reveals a previously uncharacterized link between essential nutrients and epigenetic regulation of plasma cell differentiation and humoral immune response.

Keywords: Ascorbic acid; B cell in vitro differentiation; Blimp-1; Epigenetic regulation; Germinal center B cell; Immune respones; Plasma B cell; Ten-eleven translocation (TET) enzymes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Ascorbic Acid / pharmacology
  • Ascorbic Acid / therapeutic use*
  • DNA Demethylation / drug effects*
  • DNA-Binding Proteins / drug effects*
  • Dioxygenases / drug effects*
  • Humans
  • Mice
  • Plasma / metabolism*

Substances

  • DNA-Binding Proteins
  • Dioxygenases
  • Tet2 protein, mouse
  • Ascorbic Acid