1?,25-dihydroxyvitamin D3 acts via transforming growth factor-? to up-regulate expression of immunosuppressive CD73 on human CD4+ Foxp3- T cells.

ABSTRACT: Vitamin D deficiency is associated with increased incidence and severity of various immune-mediated diseases. Active vitamin D (1?,25-dihydroxyvitamin D3; 1,25(OH)2 D3) up-regulates CD4(+) T-cell expression of the purine ectonucleotidase CD39, a molecule that is associated with the generation of anti-inflammatory adenosine. Here we aimed to investigate the direct impact of 1,25(OH)2 D3 on expression of the downstream ecto-5'-nucleotidase CD73 by human CD4 T cells, and components of the transforming growth factor-? (TGF-?) pathway, which have been implicated in the modulation of CD73 by murine T cells. At 10(-8) to 10(-7) m, 1,25(OH)2 D3 significantly increased expression of CD73 on peripheral human CD4(+) T cells. Although 1,25(OH)2 D3 did not affect the mRNA expression of latent TGF-?1 , 1,25(OH)2 D3 did up-regulate expression of TGF-?-associated molecules [latency-associated peptide (LAP), glycophorin A repetitions predominant (GARP), GP96, neuropilin-1, thrombospondin-1 and ?v integrin] which is likely to have contributed to the observed enhancement in TGF-? bioactivity. CD73 was highly co-expressed with LAP and GARP following 1,25(OH)2 D3 treatment, but unexpectedly, each of these cell surface molecules was expressed primarily on CD4(+) Foxp3(-) T cells, rather than CD4(+) Foxp3(+) T cells. Notably, neutralization of TGF-? significantly impaired 1,25(OH)2 D3-mediated induction of CD73. Collectively, we show that 1,25(OH)2 D3 enhances expression of CD73 on CD4(+) Foxp3(-) T cells in a process that is at least partially TGF-?-dependent. These data reveal an additional contributing mechanism by which vitamin D may be protective in immune-mediated disease.

SUBMITTER: Mann EH 

PROVIDER: S-EPMC4610631 | biostudies-literature | 2015 Nov

REPOSITORIES: biostudies-literature