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Detection of Succinate by Intestinal Tuft Cells Triggers a Type 2 Innate Immune Circuit.
Nadjsombati, Marija S; McGinty, John W; Lyons-Cohen, Miranda R; Jaffe, James B; DiPeso, Lucian; Schneider, Christoph; Miller, Corey N; Pollack, Joshua L; Nagana Gowda, G A; Fontana, Mary F; Erle, David J; Anderson, Mark S; Locksley, Richard M; Raftery, Daniel; von Moltke, Jakob.
Afiliación
  • Nadjsombati MS; Department of Immunology, University of Washington School of Medicine, Seattle, WA 98109, USA.
  • McGinty JW; Department of Immunology, University of Washington School of Medicine, Seattle, WA 98109, USA.
  • Lyons-Cohen MR; Department of Immunology, University of Washington School of Medicine, Seattle, WA 98109, USA.
  • Jaffe JB; Department of Immunology, University of Washington School of Medicine, Seattle, WA 98109, USA.
  • DiPeso L; Department of Immunology, University of Washington School of Medicine, Seattle, WA 98109, USA.
  • Schneider C; Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94143, USA; Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA
  • Miller CN; Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA; Diabetes Center, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Pollack JL; Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Nagana Gowda GA; Northwest Metabolomics Research Center, Department of Anesthesiology and Pain Medicine, University of Washington, Seattle, WA 98109, USA.
  • Fontana MF; Department of Immunology, University of Washington School of Medicine, Seattle, WA 98109, USA.
  • Erle DJ; Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Anderson MS; Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94143, USA; Diabetes Center, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Locksley RM; Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94143, USA; Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA
  • Raftery D; Northwest Metabolomics Research Center, Department of Anesthesiology and Pain Medicine, University of Washington, Seattle, WA 98109, USA.
  • von Moltke J; Department of Immunology, University of Washington School of Medicine, Seattle, WA 98109, USA. Electronic address: jmoltke@uw.edu.
Immunity ; 49(1): 33-41.e7, 2018 07 17.
Article en En | MEDLINE | ID: mdl-30021144
In the small intestine, type 2 responses are regulated by a signaling circuit that involves tuft cells and group 2 innate lymphoid cells (ILC2s). Here, we identified the microbial metabolite succinate as an activating ligand for small intestinal (SI) tuft cells. Sequencing analyses of tuft cells isolated from the small intestine, gall bladder, colon, thymus, and trachea revealed that expression of tuft cell chemosensory receptors is tissue specific. SI tuft cells expressed the succinate receptor (SUCNR1), and providing succinate in drinking water was sufficient to induce a multifaceted type 2 immune response via the tuft-ILC2 circuit. The helminth Nippostrongylus brasiliensis and a tritrichomonad protist both secreted succinate as a metabolite. In vivo sensing of the tritrichomonad required SUCNR1, whereas N. brasiliensis was SUCNR1 independent. These findings define a paradigm wherein tuft cells monitor microbial metabolites to initiate type 2 immunity and suggest the existence of other sensing pathways triggering the response to helminths.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Transducción de Señal / Inmunidad Mucosa / Ácido Succínico / Receptores Acoplados a Proteínas G / Mucosa Intestinal Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Animals Idioma: En Revista: Immunity Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Transducción de Señal / Inmunidad Mucosa / Ácido Succínico / Receptores Acoplados a Proteínas G / Mucosa Intestinal Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Animals Idioma: En Revista: Immunity Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos