Your browser doesn't support javascript.
loading
Human RORγt(+)CD34(+) cells are lineage-specified progenitors of group 3 RORγt(+) innate lymphoid cells.
Montaldo, Elisa; Teixeira-Alves, Luiz Gustavo; Glatzer, Timor; Durek, Pawel; Stervbo, Ulrik; Hamann, Wiebke; Babic, Marina; Paclik, Daniela; Stölzel, Katharina; Gröne, Jörn; Lozza, Laura; Juelke, Kerstin; Matzmohr, Nadine; Loiacono, Fabrizio; Petronelli, Francesca; Huntington, Nicholas David; Moretta, Lorenzo; Mingari, Maria Cristina; Romagnani, Chiara.
Afiliación
  • Montaldo E; Department of Experimental Medicine, University of Genova, Via LB Alberti 2, 16132 Genova, Italy; UOC Immunologia, IRCCS-AOU-San Martino-IST, L.go R. Benzi 10, 16132 Genova, Italy.
  • Teixeira-Alves LG; Innate Immunity, Deutsches Rheuma Forschungszentrum (DRFZ) Berlin, Leibniz-Gemeinschaft, Charitéplatz 1, 10117 Berlin, Germany.
  • Glatzer T; Innate Immunity, Deutsches Rheuma Forschungszentrum (DRFZ) Berlin, Leibniz-Gemeinschaft, Charitéplatz 1, 10117 Berlin, Germany.
  • Durek P; Cell Biology, Deutsches Rheuma Forschungszentrum (DRFZ) Berlin, Leibniz-Gemeinschaft, Charitéplatz 1, 10117 Berlin, Germany.
  • Stervbo U; Cell Biology, Deutsches Rheuma Forschungszentrum (DRFZ) Berlin, Leibniz-Gemeinschaft, Charitéplatz 1, 10117 Berlin, Germany.
  • Hamann W; Innate Immunity, Deutsches Rheuma Forschungszentrum (DRFZ) Berlin, Leibniz-Gemeinschaft, Charitéplatz 1, 10117 Berlin, Germany.
  • Babic M; Innate Immunity, Deutsches Rheuma Forschungszentrum (DRFZ) Berlin, Leibniz-Gemeinschaft, Charitéplatz 1, 10117 Berlin, Germany; Department of Histology and Embryology, Faculty of Medicine, University of Rijeka, B. Branchetta 20a, 51000 Rijeka, Croatia.
  • Paclik D; Innate Immunity, Deutsches Rheuma Forschungszentrum (DRFZ) Berlin, Leibniz-Gemeinschaft, Charitéplatz 1, 10117 Berlin, Germany.
  • Stölzel K; HNO-Klinik-Charité-Universitätsmedizin, Charitéplatz 1, 10117 Berlin, Germany.
  • Gröne J; Klinik für Allgemein-, Gefäß- und Thoraxchirurgie Charité-Universitätsmedizin, Hindenburgdamm 30, 12203 Berlin, Germany.
  • Lozza L; Department of Immunology, Max Planck Institute for Infection Biology, Charitéplatz 1, 10117 Berlin, Germany.
  • Juelke K; Innate Immunity, Deutsches Rheuma Forschungszentrum (DRFZ) Berlin, Leibniz-Gemeinschaft, Charitéplatz 1, 10117 Berlin, Germany; Immune System, Berlin-Brandenburg Center for Regenerative Therapies (BCRT) Charité-Universitätsmedizin, Augustenburger Platz 1, 13353 Berlin, Germany.
  • Matzmohr N; Immune Regeneration and Aging, Berlin-Brandenburg Center for Regenerative Therapies (BCRT) Charité-Universitätsmedizin, Augustenburger Platz 1, 13353 Berlin, Germany.
  • Loiacono F; Giannina Gaslini Institute, Via G. Gaslini 5, 16147 Genova, Italy.
  • Petronelli F; Giannina Gaslini Institute, Via G. Gaslini 5, 16147 Genova, Italy.
  • Huntington ND; Department of Medical Biology, The Walter and Eliza Hall Institute of Medical Research, The University of Melbourne, 1G Royal Parade, Parkville, VIC 3052, Australia.
  • Moretta L; Giannina Gaslini Institute, Via G. Gaslini 5, 16147 Genova, Italy.
  • Mingari MC; Department of Experimental Medicine, University of Genova, Via LB Alberti 2, 16132 Genova, Italy; UOC Immunologia, IRCCS-AOU-San Martino-IST, L.go R. Benzi 10, 16132 Genova, Italy.
  • Romagnani C; Innate Immunity, Deutsches Rheuma Forschungszentrum (DRFZ) Berlin, Leibniz-Gemeinschaft, Charitéplatz 1, 10117 Berlin, Germany. Electronic address: romagnani@drfz.de.
Immunity ; 41(6): 988-1000, 2014 Dec 18.
Article en En | MEDLINE | ID: mdl-25500367
ABSTRACT
Group 3 innate lymphoid cells (ILC3s) are defined by the expression of the transcription factor RORγt, which is selectively required for their development. The lineage-specified progenitors of ILC3s and their site of development after birth remain undefined. Here we identified a population of human CD34(+) hematopoietic progenitor cells (HPCs) that express RORγt and share a distinct transcriptional signature with ILC3s. RORγt(+)CD34(+) HPCs were located in tonsils and intestinal lamina propria (LP) and selectively differentiated toward ILC3s. In contrast, RORγt(-)CD34(+) HPCs could differentiate to become either ILC3s or natural killer (NK) cells, with differentiation toward ILC3 lineage determined by stem cell factor (SCF) and aryl hydrocarbon receptor (AhR) signaling. Thus, we demonstrate that in humans RORγt(+)CD34(+) cells are lineage-specified progenitors of IL-22(+) ILC3s and propose that tonsils and intestinal LP, which are enriched both in committed precursors and mature ILC3s, might represent preferential sites of ILC3 lineage differentiation.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Células Madre Hematopoyéticas / Linfocitos / Miembro 3 del Grupo F de la Subfamilia 1 de Receptores Nucleares Tipo de estudio: Prognostic_studies Límite: Adult / Humans Idioma: En Revista: Immunity Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2014 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Células Madre Hematopoyéticas / Linfocitos / Miembro 3 del Grupo F de la Subfamilia 1 de Receptores Nucleares Tipo de estudio: Prognostic_studies Límite: Adult / Humans Idioma: En Revista: Immunity Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2014 Tipo del documento: Article País de afiliación: Italia