| Literature DB >> 28329707 |
Tomer Granot1, Takashi Senda2, Dustin J Carpenter2, Nobuhide Matsuoka2, Joshua Weiner3, Claire L Gordon1, Michelle Miron4, Brahma V Kumar5, Adam Griesemer2, Siu-Hong Ho4, Harvey Lerner6, Joseph J C Thome4, Thomas Connors7, Boris Reizis8, Donna L Farber9.
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.Entities:
Keywords: dendritic cells; human immunology; mucosal immunity; tissue immunity
Mesh:
Year: 2017 PMID: 28329707 PMCID: PMC5415308 DOI: 10.1016/j.immuni.2017.02.019
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745