The transcriptional regulator Aire co-opts the repressive ATF7ip-MBD1 complex for induction of immune tolerance

The maintenance of immune tolerance requires the deletion of self-reactive T cells in the thymus. The expression of tissue-specific antigen genes (TSAs) by thymic epithelial cells is critical for this process and depends on the activity of the Autoimmune Regulator (Aire) protein, however, the molecu...

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Veröffentlicht in:Nature immunology 2014-01, Vol.15 (3), p.258-265
Hauptverfasser: Waterfield, Michael, Khan, Imran S., Cortez, Jessica T., Fan, Una, Metzger, Todd, Greer, Alexandra, Fasano, Kayla, Martinez-Llordella, Marc, Pollack, Joshua L., Erle, David J., Su, Maureen, Anderson, Mark S.
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Sprache:eng
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Zusammenfassung:The maintenance of immune tolerance requires the deletion of self-reactive T cells in the thymus. The expression of tissue-specific antigen genes (TSAs) by thymic epithelial cells is critical for this process and depends on the activity of the Autoimmune Regulator (Aire) protein, however, the molecular mechanism(s) Aire uses to target TSA gene loci are unknown. Here we identified two Aire-interacting proteins – activating transcription factor 7 interacting protein (ATF7ip) and methyl CpG binding protein 1 (MBD1) –that are required for Aire’s targeting of TSA geneloci. Moreover, Mbd1 −/− mice developed pathological autoimmunity and had a defect in Aire-dependent thymic TSA gene expression underscoring the critical importance of Aire’s interaction with the ATF7ip-MBD1 protein complex in maintaining central tolerance.
ISSN:1529-2908
1529-2916
DOI:10.1038/ni.2820