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Each of our data claim that active 1, 25D signaling enriched Aire+ mTECs and enhanced the colocalization with the transcription factor Vdr. The just a few overlap between your binding sites of the two proteins can be consistent with the pleiotropic actions of both substances and shows that they may work together functionally. you, 25D enhanced the expression of Aire mRNA and increased the number of Aire+ cells in thymic slices, and caused Aire-dependent COMPRESA TRA mRNAs in sorted TEC populations. you, 25D treatment also increased Vdr colocalization with Castillo in mTECs, cTECs, and thymocytes.
We confirmed that intestinal epithelial VDR regulates autophagy through its interaction with all the protein ATG16L1 and that reduced intestinal VDR expression correlates with dysbiosis in a colitis model. Supervision of the microbial product butyrate increases digestive tract epithelial VDR expression and restores microbial homeostasis. This is actually first demo that VDR impact on the intestinal microbiome through its relationship with ATG16L1 and autophagy. We propose that intestinal epithelial VDR is a primary regulator of intestinal homeostasis and that modulation of this receptor could be an powerful therapeutic technique to treat inflammatory bowel disease.