Academic Journal

Indoleamine 2,3-dioxygenase is a signaling protein in long-term tolerance by dendritic cells

التفاصيل البيبلوغرافية
العنوان: Indoleamine 2,3-dioxygenase is a signaling protein in long-term tolerance by dendritic cells
المؤلفون: PALLOTTA, MARIA TERESA, ORABONA, Ciriana, VOLPI, CLAUDIA, VACCA, Carmine, BELLADONNA, Maria Laura, BIANCHI, Roberta, SERVILLO, Giuseppe, BRUNACCI, CINZIA, CALVITTI, Mario, S. Bicciato, E. M. Mazza, L. Boon, F. Grassi, FIORETTI, Maria Cristina, FALLARINO, Francesca, PUCCETTI, Paolo, GROHMANN, Ursula
المساهمون: Pallotta, MARIA TERESA, Orabona, Ciriana, Volpi, Claudia, Vacca, Carmine, Belladonna, Maria Laura, Bianchi, Roberta, Servillo, Giuseppe, Brunacci, Cinzia, Calvitti, Mario, S., Bicciato, E. M., Mazza, L., Boon, F., Grassi, Fioretti, Maria Cristina, Fallarino, Francesca, Puccetti, Paolo, Grohmann, Ursula
سنة النشر: 2011
المجموعة: IRIS Università degli Studi di Perugia
مصطلحات موضوعية: IDO, indoleamine 2, 3-dioxygenase, tryptophan catabolism, dendritic cell, immune regulation
الوصف: Regulation of tryptophan metabolism by indoleamine 2,3-dioxygenase (IDO) in dendritic cells (DCs) is a highly versatile modulator of immunity. In inflammation, interferon-γ is the main inducer of IDO for the prevention of hyperinflammatory responses, yet IDO is also responsible for self-tolerance effects in the longer term. Here we show that treatment of mouse plasmacytoid DCs (pDCs) with transforming growth factor-β (TGF-β) conferred regulatory effects on IDO that were mechanistically separable from its enzymic activity. We found that IDO was involved in intracellular signaling events responsible for the self-amplification and maintenance of a stably regulatory phenotype in pDCs. Thus, IDO has a tonic, nonenzymic function that contributes to TGF-β-driven tolerance in noninflammatory contexts.
نوع الوثيقة: article in journal/newspaper
وصف الملف: ELETTRONICO
اللغة: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/21804557; info:eu-repo/semantics/altIdentifier/wos/WOS:000294461200011; volume:12; issue:9; firstpage:870; lastpage:878; numberofpages:9; journal:NATURE IMMUNOLOGY; http://hdl.handle.net/11391/409095; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-80052020183; https://www.nature.com/articles/ni.2077
DOI: 10.1038/ni.2077
الاتاحة: http://hdl.handle.net/11391/409095
https://doi.org/10.1038/ni.2077
https://www.nature.com/articles/ni.2077
رقم الانضمام: edsbas.EFB18B8E
قاعدة البيانات: BASE