Nuclear factor of activated T cells as a marker of in vivo low‐dose dibenzo[a,h]anthracene exposure

We previously demonstrated that particulate matter ≤2.5 μm (PM2.5) suppresses the immune response in the spleen in vivo. Although PM2.5 includes the polycyclic aromatic hydrocarbon (PAH) such as dibenzo[a,h]anthracene (DBA), it is unclear whether PAH has a direct effect on the responses of splenocytes. In our study, the concentration of DBA used was approximately 0.8 μm, which is much lower than concentrations used in other toxicological studies of DBA. Although exposure to high concentrations of DBA is implicated in carcinogenesis, the effects of low doses of DBA on immune cells in vivo remain unclear. Here, we investigated the effects of low DBA doses on mouse splenocytes in vivo. Mice were administered dimethyl sulfoxide or DBA (0.4 or 0.8 μm) intratracheally. Twenty‐four hours after treatment, the mice were killed and their splenocytes were collected. DBA treatment enhanced mitogen‐induced cell proliferation and cytokine production in the mouse splenocytes. Furthermore, DBA enhanced splenic CD4+ and CD8+ cell proliferation and cytokine production. The nuclear factor of activated T cells (NFAT) was activated in CD4+ cells. DBA also activated nuclear factor‐kappa B and CCAAT enhancer‐binding protein pathways in CD11b+ cells. DBA‐enhanced splenocyte activation was Toll‐like receptor 2‐, 4‐, 9‐ and MyD88‐independent. These results suggest that NFAT represents a promising marker for evaluation of the effects of DBA on T cells and T‐cell‐dependent antibody responses. Dibenzo[a,h]anthracene (DBA) adheres to particulate matter ≤2.5 μm. Here, we investigated the in vivo effects of low DBA doses on mouse splenocytes. DBA enhanced CD4+ and CD8+ cell proliferation and cytokine production. Nuclear factor of activated T cells (NFAT) was activated in CD4+ cells, and the nuclear factor‐kappaB and C/EBP pathways were activated in CD11b+ cells. These effects were Toll‐like‐receptor‐independent. NFAT is a promising marker for evaluating the effects of polycyclic aromatic hydrocarbon exposure on T cells and T‐cell‐dependent antibody responses.