A1 Refereed original research article in a scientific journal
Embryonic macrophages function during early life to determine invariant natural killer T cell levels at barrier surfaces
Authors: Gensollen Thomas, Lin Xi, Zhang Ting, Pyzik Michal, See Peter, Glickman Jonathan N, Ginhoux Florent, Waldor Matthew, Salmi Marko, Rantakari Pia, Blumberg Richard S
Publisher: NATURE RESEARCH
Publication year: 2021
Journal: Nature Immunology
Journal name in source: NATURE IMMUNOLOGY
Journal acronym: NAT IMMUNOL
Volume: 22
First page : 699
Last page: 710
Number of pages: 31
ISSN: 1529-2908
eISSN: 1529-2916
DOI: https://doi.org/10.1038/s41590-021-00934-0
Self-archived copy’s web address: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8171892/
Abstract
It is increasingly recognized that immune development within mucosal tissues is under the control of environmental factors during early life. However, the cellular mechanisms that underlie such temporally and regionally restrictive governance of these processes are unclear. Here, we uncover an extrathymic pathway of immune development within the colon that is controlled by embryonic but not bone marrow-derived macrophages, which determines the ability of these organs to receive invariant natural killer T (iNKT) cells and allow them to establish local residency. Consequently, early-life perturbations of fetal-derived macrophages result in persistent decreases of mucosal iNKT cells and is associated with later-life susceptibility or resistance to iNKT cell-associated mucosal disorders. These studies uncover a host developmental program orchestrated by ontogenically distinct macrophages that is regulated by microbiota, and they reveal an important postnatal function of macrophages that emerge in fetal life.Invariant natural killer T (iNKT) cells populate barrier surfaces during an early-life window. Blumberg and colleagues demonstrate that such barrier surface iNKT cells develop via an extrathymic pathway dependent on a specialized population of embryo-derived macrophages.
It is increasingly recognized that immune development within mucosal tissues is under the control of environmental factors during early life. However, the cellular mechanisms that underlie such temporally and regionally restrictive governance of these processes are unclear. Here, we uncover an extrathymic pathway of immune development within the colon that is controlled by embryonic but not bone marrow-derived macrophages, which determines the ability of these organs to receive invariant natural killer T (iNKT) cells and allow them to establish local residency. Consequently, early-life perturbations of fetal-derived macrophages result in persistent decreases of mucosal iNKT cells and is associated with later-life susceptibility or resistance to iNKT cell-associated mucosal disorders. These studies uncover a host developmental program orchestrated by ontogenically distinct macrophages that is regulated by microbiota, and they reveal an important postnatal function of macrophages that emerge in fetal life.Invariant natural killer T (iNKT) cells populate barrier surfaces during an early-life window. Blumberg and colleagues demonstrate that such barrier surface iNKT cells develop via an extrathymic pathway dependent on a specialized population of embryo-derived macrophages.
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