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Dendritic Cells Display Subset and Tissue-Specific Maturation Dynamics over Human Life.
Granot, Tomer; Senda, Takashi; Carpenter, Dustin J; Matsuoka, Nobuhide; Weiner, Joshua; Gordon, Claire L; Miron, Michelle; Kumar, Brahma V; Griesemer, Adam; Ho, Siu-Hong; Lerner, Harvey; Thome, Joseph J C; Connors, Thomas; Reizis, Boris; Farber, Donna L.
Affiliation
  • Granot T; Columbia Center for Translational Immunology, Columbia University Medical Center, New York, NY 10032, USA; Department of Medicine, Columbia University Medical Center, New York, NY 10032, USA.
  • Senda T; Columbia Center for Translational Immunology, Columbia University Medical Center, New York, NY 10032, USA; Department of Surgery, Columbia University Medical Center, New York, NY 10032, USA.
  • Carpenter DJ; Columbia Center for Translational Immunology, Columbia University Medical Center, New York, NY 10032, USA; Department of Surgery, Columbia University Medical Center, New York, NY 10032, USA.
  • Matsuoka N; Columbia Center for Translational Immunology, Columbia University Medical Center, New York, NY 10032, USA; Department of Surgery, Columbia University Medical Center, New York, NY 10032, USA.
  • Weiner J; Department of Surgery, Columbia University Medical Center, New York, NY 10032, USA.
  • Gordon CL; Columbia Center for Translational Immunology, Columbia University Medical Center, New York, NY 10032, USA; Department of Medicine, Columbia University Medical Center, New York, NY 10032, USA.
  • Miron M; Columbia Center for Translational Immunology, Columbia University Medical Center, New York, NY 10032, USA; Department of Microbiology and Immunology, Columbia University Medical Center, New York, NY 10032, USA.
  • Kumar BV; Columbia Center for Translational Immunology, Columbia University Medical Center, New York, NY 10032, USA.
  • Griesemer A; Columbia Center for Translational Immunology, Columbia University Medical Center, New York, NY 10032, USA; Department of Surgery, Columbia University Medical Center, New York, NY 10032, USA.
  • Ho SH; Columbia Center for Translational Immunology, Columbia University Medical Center, New York, NY 10032, USA; Department of Microbiology and Immunology, Columbia University Medical Center, New York, NY 10032, USA.
  • Lerner H; LiveOnNY, New York, NY 10001, USA.
  • Thome JJC; Columbia Center for Translational Immunology, Columbia University Medical Center, New York, NY 10032, USA; Department of Microbiology and Immunology, Columbia University Medical Center, New York, NY 10032, USA.
  • Connors T; Columbia Center for Translational Immunology, Columbia University Medical Center, New York, NY 10032, USA; Division of Critical Care, Department of Pediatrics, Columbia University Medical Center, New York, NY 10032, USA.
  • Reizis B; Department of Pathology, NYU Langone Medical Center, New York, NY 10016, USA.
  • Farber DL; Columbia Center for Translational Immunology, Columbia University Medical Center, New York, NY 10032, USA; Department of Surgery, Columbia University Medical Center, New York, NY 10032, USA; Department of Microbiology and Immunology, Columbia University Medical Center, New York, NY 10032, USA. Elect
Immunity ; 46(3): 504-515, 2017 03 21.
Article in En | MEDLINE | ID: mdl-28329707
ABSTRACT
Maturation and migration to lymph nodes (LNs) constitutes a central paradigm in conventional dendritic cell (cDC) biology but remains poorly defined in humans. Using our organ donor tissue resource, we analyzed cDC subset distribution, maturation, and migration in mucosal tissues (lungs, intestines), associated lymph nodes (LNs), and other lymphoid sites from 78 individuals ranging from less than 1 year to 93 years of age. The distribution of cDC1 (CD141hiCD13hi) and cDC2 (Sirp-α+CD1c+) subsets was a function of tissue site and was conserved between donors. We identified cDC2 as the major mature (HLA-DRhi) subset in LNs with the highest frequency in lung-draining LNs. Mature cDC2 in mucosal-draining LNs expressed tissue-specific markers derived from the paired mucosal site, reflecting their tissue-migratory origin. These distribution and maturation patterns were largely maintained throughout life, with site-specific variations. Our findings provide evidence for localized DC tissue surveillance and reveal a lifelong division of labor between DC subsets, with cDC2 functioning as guardians of the mucosa.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dendritic Cells Type of study: Prognostic_studies Limits: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Immunity Journal subject: ALERGIA E IMUNOLOGIA Year: 2017 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dendritic Cells Type of study: Prognostic_studies Limits: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Immunity Journal subject: ALERGIA E IMUNOLOGIA Year: 2017 Document type: Article Affiliation country: United States