We have recently shown that the transplantation of BM transduced with pMog promotes deletional tolerance and prevents development of the MOG35–55-induced EAE in C57BL/6 mice 29. Given that the ectopic expression of AIRE can induce expression of TRA, including Venetoclax in vitro MOG in vitro, we asked whether the transplantation of retrovirally transduced BM cells expressing AIRE in syngeneic animals altered the course of EAE in animals immunized with MOG35–55. The level of chimerism was analysed 10 weeks following the transplantation of transduced BM cells by assessing the percentage

of GFP+ cells from the thymus and spleen. The GFP expression was detected in all the major cell lineages examined, including

CD4+and CD8+ T cells, B cells and MHC class II+ CD11c+ dendritic cells (Fig. 3A, Supporting Information Fig. 1 for gating strategy). RT-PCR analysis of thymus samples from Aire chimeric mice revealed increased levels of Aire, Mog and Ins2 mRNA compared with thymi from mice transplanted with normal BM or from untouched WT mice, suggesting that the AIRE expression AUY-922 ic50 has upmodulated these two defined autoantigens (Fig. 3B). While attempted, we were not able to accurately quantify and compare the MOG expression in the thymus across normal mice, mice transplanted with normal BM or Aire-transduced BM. To demonstrate differential expression of Aire and TRA in cells originating from transduced BM cells, GFP+ cells were enriched from the spleens of chimeric mice. Comparison Sucrase of GFP+ and GFP- cells indicated a greater level of AIRE expression in GFP+ cells, consistent with retroviral promoter-driven expression within these cells. Further analysis revealed elevated levels of Mog and Ins2 mRNA in GFP+ cells compared with GFP- cells (Fig. 3C). These data support our in vitro findings that the ectopic expression of AIRE can promote the expression of TRA including the autoantigens Mog and Ins2. We next determined whether the intrathymic expression of the EAE/MS associated autoantigens

Mog, Plp and Mbp was AIRE dependent. MHCIIhi mTEC (CD45–, Ly51–, MHCIIhi) from WT and Aire−/− C57BL/6 mice were isolated and qRT-PCR revealed a marked reduction in the expression of MOG (to 25% WT levels) and Plp (to 12% WT levels) in Aire−/− mTEC with no change in Mbp expression (Fig. 4A). While Mog has previously been reported as being AIRE dependent, PLP was reported to be AIRE independent 39. However, these data came from human association studies of AIRE and TRA expression rather than from the examination of AIRE-deficient thymi and could thus explain the discrepancy in result for PLP. Given the observed reduction in Mog expression, we asked whether Aire−/− mice were more susceptible to MOG-induced EAE than WT C57BL/6 mice.