A crucial role for retinoic acid in the development of Notch-dependent murine splenic CD8- CD4- and CD4+ dendritic cells

Eur J Immunol. 2013 Jun;43(6):1608-16. doi: 10.1002/eji.201343325. Epub 2013 Apr 27.

Abstract

The vitamin A metabolite retinoic acid is important for the function of the adaptive immune system, but the mechanism is not completely understood. Here we show that vitamin A is essential for the generation of Notch-dependent CD8(-) dendritic cells (DCs) in the spleen. We observed that CD8(-) CD4(-) (double negative (DN)) and CD4(+) DCs, but not CD8(+) DCs, express vitamin A regulated genes. To determine whether vitamin A levels influence splenic DC development, we generated mice that were fed a vitamin A-deficient diet. We detected a specific reduction of CD4(+) and DN DCs in the spleens of mice fed a vitamin A-deficient diet, while pre-DC numbers in both spleen and bone marrow were not affected. Vitamin A was specifically necessary for the development of RelB(high) , Notch-dependent CD4(+) , and DN DCs. In addition, DN DCs showed reduced proliferation during vitamin A deficiency. In contrast, mice that had received a diet with increased amounts of retinoic acid showed a significant expansion of Notch-dependent DN DCs. These data demonstrate that vitamin A stimulates the development of Notch-dependent splenic DCs and indicate that inefficient generation of DCs may contribute to the immune deficits observed during vitamin A deficiency.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD4 Antigens / immunology
  • CD8 Antigens / immunology
  • Cell Differentiation
  • Cell Lineage
  • Cell Proliferation
  • Dendritic Cells / immunology*
  • Feeding Behavior
  • Female
  • Mice
  • Mice, Inbred C57BL
  • Pregnancy
  • Receptors, Notch / metabolism
  • Spleen / cytology
  • Transcription Factor RelB / metabolism
  • Tretinoin / immunology*
  • Vitamin A Deficiency / immunology*

Substances

  • CD4 Antigens
  • CD8 Antigens
  • Receptors, Notch
  • Relb protein, mouse
  • Transcription Factor RelB
  • Tretinoin