To further understand the delayed inducing effects of simvastatin, we added simvastatin at different time-points after the initiation of TCR stimulation with TGF-β or added simvastatin at culture initiation and then blocked its action at different time-points by the addition of mevalonate. All cultures were analysed for the expression of Foxp3+ cells after 72 hr of stimulation (Fig. 4b). The maximal inducing

effects of simvastatin could be observed even when it was added as late as 24 hr after the initiation of the cultures, but its synergistic activity was completely abolished when it was added after 48 hr (Fig. 4b). Similarly, the neutralization of the effects AZD6244 mouse of simvastatin with mevalonate was only observed when mevalonate was added during the first 24–32 hr of the culture.

This study suggested that simvastatin mediated its activity between 24 and 48 hr after T-cell activation. We confirmed this result by adding simvastatin at 24 hr and neutralizing its effects with mevalonate at 48 hr (Fig. 4c). The magnitude of the enhancement of the induction of Foxp3-expressing cells was similar in cells pulse-exposed to simvastatin only between 24 and 48 hr after activation to that in cells that had been exposed for the entire 72-hr culture period. To address whether synergistic action of simvastatin on TGF-β-mediated induction is controlled at the transcriptional level, we assayed the Foxp3 messenger RNA (mRNA) levels in cells treated with TGF-β alone or with the combination of TGF-β and simvastatin (Fig. 5a). Up-regulation of Foxp3 mRNA was observed after 24 hr of culture in the TGFβ only treated group compared to cells selleck inhibitor cultured with vehicle alone and no enhancement of Foxp3 mRNA was seen in cultures with simvastatin. In contrast, marked enhancement of Foxp3 mRNA levels were seen after 48 and 72 hr in cultures containing both TGF-β and simvastatin, whereas levels of Foxp3 mRNA in cultures with TGF-β alone were slightly diminished. This result together with the results of the time–course study strongly suggest that

the effects of simvastatin are not related to enhancement of the initial Selleckchem Paclitaxel signals induced by TGF-β and raise the possibility that simvastatin might regulate epigenetic control of Foxp3 transcription. Recent studies6,15 have identified two or three CpG islands within the promoter and enhancer regions of the Foxp3 gene that regulate the induction of Foxp3 transcription and the stabilization of Foxp3 expression. We focused on one site in the Foxp3 promoter that contains six CpGs within a 173-base-pair sequence of the mouse Foxp3 promoter that are located close to the proximal transcription start site. To verify if this candidate site is specific for Foxp3 promoter activity, Foxp3− and Foxp3+ CD4+ cells were isolated from Foxp3gfp male mice, and methylation profiles of both were analysed by bisulphite-modified sequence reading.