| Literature DB >> 30173915 |
Sebastiaan De Schepper1, Simon Verheijden1, Javier Aguilera-Lizarraga1, Maria Francesca Viola1, Werend Boesmans2, Nathalie Stakenborg1, Iryna Voytyuk3, Inga Schmidt3, Bram Boeckx4, Isabelle Dierckx de Casterlé5, Veerle Baekelandt6, Erika Gonzalez Dominguez1, Matthias Mack7, Inge Depoortere8, Bart De Strooper9, Ben Sprangers5, Uwe Himmelreich10, Stefaan Soenen10, Martin Guilliams11, Pieter Vanden Berghe2, Elizabeth Jones12, Diether Lambrechts4, Guy Boeckxstaens13.
Abstract
Macrophages are highly heterogeneous tissue-resident immune cells that perform a variety of tissue-supportive functions. The current paradigm dictates that intestinal macrophages are continuously replaced by incoming monocytes that acquire a pro-inflammatory or tissue-protective signature. Here, we identify a self-maintaining population of macrophages that arise from both embryonic precursors and adult bone marrow-derived monocytes and persists throughout adulthood. Gene expression and imaging studies of self-maintaining macrophages revealed distinct transcriptional profiles that reflect their unique localization (i.e., closely positioned to blood vessels, submucosal and myenteric plexus, Paneth cells, and Peyer's patches). Depletion of self-maintaining macrophages resulted in morphological abnormalities in the submucosal vasculature and loss of enteric neurons, leading to vascular leakage, impaired secretion, and reduced intestinal motility. These results provide critical insights in intestinal macrophage heterogeneity and demonstrate the strategic role of self-maintaining macrophages in gut homeostasis and intestinal physiology.Entities:
Keywords: enteric nervous system; fate mapping; gene profiling; intestinal macrophage; intestinal macrophage heterogeneity; intestinal macrophage ontogeny; intestinal transit; neuro-immune interactions; neurodegeneration
Mesh:
Year: 2018 PMID: 30173915 DOI: 10.1016/j.cell.2018.07.048
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582