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Human Liver Macrophage Subsets Defined by CD32

Authors :
Ian N Crispe
Xia Wu
Nicole Hollingshead
Helen Horton
Antony K. Chen
Allison Knupp
Raymond S. Yeung
Heidi L. Kenerson
Ian Strickland
Jessica Roberto
Radika Soysa
Source :
Frontiers in Immunology, Vol 11 (2020), Frontiers in Immunology
Publication Year :
2020
Publisher :
Frontiers Media S.A., 2020.

Abstract

Human liver myeloid cells are imperfectly defined, but it is broadly agreed that cells of stellate appearance in situ, expressing the markers CD11b and CD68, are the liver's resident macrophages, classically termed Kupffer cells. Recent investigations using single cell RNA sequencing and unsupervised clustering algorithms suggest there are two populations of cells with the characteristics of tissue macrophages in human liver. We therefore analyzed dissociated human liver tissue using the markers CD11b and CD68 to define macrophage-like cells and found within this population two subsets that differ in their expression of multiple surface markers. These subsets were FACS-sorted based on CD32 expression, and gene expression analysis identified them with human liver myeloid cell subsets that were previously defined by two independent single cell RNA sequencing studies. Using qRT-PCR we found that the two subsets differed in the expression of genes associated with T cell activation and immunosuppression, suggesting distinct roles in T cell tolerance. In addition, one subset expressed two markers, CD1C and CD11c, more often seen on classical dendritic cells. Criteria used to distinguish macrophages from dendritic cells in other tissues may need to be revised in the human liver.

Details

Language :
English
ISSN :
16643224
Volume :
11
Database :
OpenAIRE
Journal :
Frontiers in Immunology
Accession number :
edsair.doi.dedup.....55731bafddf9e82f51e6cc366215e187