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Tongue immune compartment analysis reveals spatial macrophage heterogeneity
The tongue is a unique muscular organ situated in the oral cavity where it is involved in taste sensation, mastication, and articulation. As a barrier organ, which is constantly exposed to environmental pathogens, the tongue is expected to host an immune cell network ensuring local immune defence. H...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9232218/ https://www.ncbi.nlm.nih.gov/pubmed/35749158 http://dx.doi.org/10.7554/eLife.77490 |
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author | Lyras, Ekaterini Maria Zimmermann, Karin Wagner, Lisa Katharina Dörr, Dorothea Klose, Christoph SN Fischer, Cornelius Jung, Steffen Yona, Simon Hovav, Avi-Hai Stenzel, Werner Dommerich, Steffen Conrad, Thomas Leutz, Achim Mildner, Alexander |
author_facet | Lyras, Ekaterini Maria Zimmermann, Karin Wagner, Lisa Katharina Dörr, Dorothea Klose, Christoph SN Fischer, Cornelius Jung, Steffen Yona, Simon Hovav, Avi-Hai Stenzel, Werner Dommerich, Steffen Conrad, Thomas Leutz, Achim Mildner, Alexander |
author_sort | Lyras, Ekaterini Maria |
collection | PubMed |
description | The tongue is a unique muscular organ situated in the oral cavity where it is involved in taste sensation, mastication, and articulation. As a barrier organ, which is constantly exposed to environmental pathogens, the tongue is expected to host an immune cell network ensuring local immune defence. However, the composition and the transcriptional landscape of the tongue immune system are currently not completely defined. Here, we characterised the tissue-resident immune compartment of the murine tongue during development, health and disease, combining single-cell RNA-sequencing with in situ immunophenotyping. We identified distinct local immune cell populations and described two specific subsets of tongue-resident macrophages occupying discrete anatomical niches. Cx3cr1(+) macrophages were located specifically in the highly innervated lamina propria beneath the tongue epidermis and at times in close proximity to fungiform papillae. Folr2(+) macrophages were detected in deeper muscular tissue. In silico analysis indicated that the two macrophage subsets originate from a common proliferative precursor during early postnatal development and responded differently to systemic LPS in vivo. Our description of the under-investigated tongue immune system sets a starting point to facilitate research on tongue immune-physiology and pathology including cancer and taste disorders. |
format | Online Article Text |
id | pubmed-9232218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-92322182022-06-25 Tongue immune compartment analysis reveals spatial macrophage heterogeneity Lyras, Ekaterini Maria Zimmermann, Karin Wagner, Lisa Katharina Dörr, Dorothea Klose, Christoph SN Fischer, Cornelius Jung, Steffen Yona, Simon Hovav, Avi-Hai Stenzel, Werner Dommerich, Steffen Conrad, Thomas Leutz, Achim Mildner, Alexander eLife Cell Biology The tongue is a unique muscular organ situated in the oral cavity where it is involved in taste sensation, mastication, and articulation. As a barrier organ, which is constantly exposed to environmental pathogens, the tongue is expected to host an immune cell network ensuring local immune defence. However, the composition and the transcriptional landscape of the tongue immune system are currently not completely defined. Here, we characterised the tissue-resident immune compartment of the murine tongue during development, health and disease, combining single-cell RNA-sequencing with in situ immunophenotyping. We identified distinct local immune cell populations and described two specific subsets of tongue-resident macrophages occupying discrete anatomical niches. Cx3cr1(+) macrophages were located specifically in the highly innervated lamina propria beneath the tongue epidermis and at times in close proximity to fungiform papillae. Folr2(+) macrophages were detected in deeper muscular tissue. In silico analysis indicated that the two macrophage subsets originate from a common proliferative precursor during early postnatal development and responded differently to systemic LPS in vivo. Our description of the under-investigated tongue immune system sets a starting point to facilitate research on tongue immune-physiology and pathology including cancer and taste disorders. eLife Sciences Publications, Ltd 2022-06-24 /pmc/articles/PMC9232218/ /pubmed/35749158 http://dx.doi.org/10.7554/eLife.77490 Text en © 2022, Lyras et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Lyras, Ekaterini Maria Zimmermann, Karin Wagner, Lisa Katharina Dörr, Dorothea Klose, Christoph SN Fischer, Cornelius Jung, Steffen Yona, Simon Hovav, Avi-Hai Stenzel, Werner Dommerich, Steffen Conrad, Thomas Leutz, Achim Mildner, Alexander Tongue immune compartment analysis reveals spatial macrophage heterogeneity |
title | Tongue immune compartment analysis reveals spatial macrophage heterogeneity |
title_full | Tongue immune compartment analysis reveals spatial macrophage heterogeneity |
title_fullStr | Tongue immune compartment analysis reveals spatial macrophage heterogeneity |
title_full_unstemmed | Tongue immune compartment analysis reveals spatial macrophage heterogeneity |
title_short | Tongue immune compartment analysis reveals spatial macrophage heterogeneity |
title_sort | tongue immune compartment analysis reveals spatial macrophage heterogeneity |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9232218/ https://www.ncbi.nlm.nih.gov/pubmed/35749158 http://dx.doi.org/10.7554/eLife.77490 |
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