Publication | Open Access
A crucial role for retinoic acid in the development of <scp>N</scp>otch‐dependent murine splenic <scp>CD</scp>8<sup>−</sup><scp>CD</scp>4<sup>−</sup> and <scp>CD</scp>4<sup>+</sup> dendritic cells
33
Citations
38
References
2013
Year
Adaptive Immune SystemInnate Immune SystemImmunologyImmune RegulationRetinoic AcidImmune SystemDn DcsCellular PhysiologyInflammationCell RegulationCell SignalingAutoimmune DiseaseAllergyCellular BiologyAutoimmunityImmune FunctionCell BiologySignal TransductionImmune Cell DevelopmentCrucial RoleDendritic Cell BiologyCellular BiochemistryMedicine
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.
| Year | Citations | |
|---|---|---|
Page 1
Page 1