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Human Liver Macrophage Subsets Defined by CD32
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 unsupe...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546764/ https://www.ncbi.nlm.nih.gov/pubmed/33101269 http://dx.doi.org/10.3389/fimmu.2020.02108 |
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author | Wu, Xia Hollingshead, Nicole Roberto, Jessica Knupp, Allison Kenerson, Heidi Chen, Antony Strickland, Ian Horton, Helen Yeung, Raymond Soysa, Radika Crispe, Ian N. |
author_facet | Wu, Xia Hollingshead, Nicole Roberto, Jessica Knupp, Allison Kenerson, Heidi Chen, Antony Strickland, Ian Horton, Helen Yeung, Raymond Soysa, Radika Crispe, Ian N. |
author_sort | Wu, Xia |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7546764 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75467642020-10-22 Human Liver Macrophage Subsets Defined by CD32 Wu, Xia Hollingshead, Nicole Roberto, Jessica Knupp, Allison Kenerson, Heidi Chen, Antony Strickland, Ian Horton, Helen Yeung, Raymond Soysa, Radika Crispe, Ian N. Front Immunol Immunology 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. Frontiers Media S.A. 2020-09-23 /pmc/articles/PMC7546764/ /pubmed/33101269 http://dx.doi.org/10.3389/fimmu.2020.02108 Text en Copyright © 2020 Wu, Hollingshead, Roberto, Knupp, Kenerson, Chen, Strickland, Horton, Yeung, Soysa and Crispe. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Wu, Xia Hollingshead, Nicole Roberto, Jessica Knupp, Allison Kenerson, Heidi Chen, Antony Strickland, Ian Horton, Helen Yeung, Raymond Soysa, Radika Crispe, Ian N. Human Liver Macrophage Subsets Defined by CD32 |
title | Human Liver Macrophage Subsets Defined by CD32 |
title_full | Human Liver Macrophage Subsets Defined by CD32 |
title_fullStr | Human Liver Macrophage Subsets Defined by CD32 |
title_full_unstemmed | Human Liver Macrophage Subsets Defined by CD32 |
title_short | Human Liver Macrophage Subsets Defined by CD32 |
title_sort | human liver macrophage subsets defined by cd32 |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546764/ https://www.ncbi.nlm.nih.gov/pubmed/33101269 http://dx.doi.org/10.3389/fimmu.2020.02108 |
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