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Th2 single-cell heterogeneity and clonal distribution at distant sites in helminth-infected mice
Th2 cells provide effector functions in type 2 immune responses to helminths and allergens. Despite knowledge about molecular mechanisms of Th2 cell differentiation, there is little information on Th2 cell heterogeneity and clonal distribution between organs. To address this, we performed combined s...
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/PMC9391044/ https://www.ncbi.nlm.nih.gov/pubmed/35950748 http://dx.doi.org/10.7554/eLife.74183 |
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author | Radtke, Daniel Thuma, Natalie Schülein, Christine Kirchner, Philipp Ekici, Arif B Schober, Kilian Voehringer, David |
author_facet | Radtke, Daniel Thuma, Natalie Schülein, Christine Kirchner, Philipp Ekici, Arif B Schober, Kilian Voehringer, David |
author_sort | Radtke, Daniel |
collection | PubMed |
description | Th2 cells provide effector functions in type 2 immune responses to helminths and allergens. Despite knowledge about molecular mechanisms of Th2 cell differentiation, there is little information on Th2 cell heterogeneity and clonal distribution between organs. To address this, we performed combined single-cell transcriptome and T-cell receptor (TCR) clonotype analysis on murine Th2 cells in mesenteric lymph nodes (MLNs) and lung after infection with Nippostrongylus brasiliensis (Nb) as a human hookworm infection model. We find organ-specific expression profiles, but also populations with conserved migration or effector/resident memory signatures that unexpectedly cluster with potentially regulatory Il10(pos)Foxp3(neg) cells. A substantial MLN subpopulation with an interferon response signature suggests a role for interferon signaling in Th2 differentiation or diversification. Further RNA-inferred developmental directions indicate proliferation as a hub for differentiation decisions. Although the TCR repertoire is highly heterogeneous, we identified expanded clones and CDR3 motifs. Clonal relatedness between distant organs confirmed effective exchange of Th2 effector cells, although locally expanded clones dominated the response. We further cloned an Nb-specific TCR from an expanded clone in the lung effector cluster and describe surface markers that distinguish transcriptionally defined clusters. These results provide insights in Th2 cell subset diversity and clonal relatedness in distant organs. |
format | Online Article Text |
id | pubmed-9391044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-93910442022-08-20 Th2 single-cell heterogeneity and clonal distribution at distant sites in helminth-infected mice Radtke, Daniel Thuma, Natalie Schülein, Christine Kirchner, Philipp Ekici, Arif B Schober, Kilian Voehringer, David eLife Immunology and Inflammation Th2 cells provide effector functions in type 2 immune responses to helminths and allergens. Despite knowledge about molecular mechanisms of Th2 cell differentiation, there is little information on Th2 cell heterogeneity and clonal distribution between organs. To address this, we performed combined single-cell transcriptome and T-cell receptor (TCR) clonotype analysis on murine Th2 cells in mesenteric lymph nodes (MLNs) and lung after infection with Nippostrongylus brasiliensis (Nb) as a human hookworm infection model. We find organ-specific expression profiles, but also populations with conserved migration or effector/resident memory signatures that unexpectedly cluster with potentially regulatory Il10(pos)Foxp3(neg) cells. A substantial MLN subpopulation with an interferon response signature suggests a role for interferon signaling in Th2 differentiation or diversification. Further RNA-inferred developmental directions indicate proliferation as a hub for differentiation decisions. Although the TCR repertoire is highly heterogeneous, we identified expanded clones and CDR3 motifs. Clonal relatedness between distant organs confirmed effective exchange of Th2 effector cells, although locally expanded clones dominated the response. We further cloned an Nb-specific TCR from an expanded clone in the lung effector cluster and describe surface markers that distinguish transcriptionally defined clusters. These results provide insights in Th2 cell subset diversity and clonal relatedness in distant organs. eLife Sciences Publications, Ltd 2022-08-11 /pmc/articles/PMC9391044/ /pubmed/35950748 http://dx.doi.org/10.7554/eLife.74183 Text en © 2022, Radtke 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 | Immunology and Inflammation Radtke, Daniel Thuma, Natalie Schülein, Christine Kirchner, Philipp Ekici, Arif B Schober, Kilian Voehringer, David Th2 single-cell heterogeneity and clonal distribution at distant sites in helminth-infected mice |
title | Th2 single-cell heterogeneity and clonal distribution at distant sites in helminth-infected mice |
title_full | Th2 single-cell heterogeneity and clonal distribution at distant sites in helminth-infected mice |
title_fullStr | Th2 single-cell heterogeneity and clonal distribution at distant sites in helminth-infected mice |
title_full_unstemmed | Th2 single-cell heterogeneity and clonal distribution at distant sites in helminth-infected mice |
title_short | Th2 single-cell heterogeneity and clonal distribution at distant sites in helminth-infected mice |
title_sort | th2 single-cell heterogeneity and clonal distribution at distant sites in helminth-infected mice |
topic | Immunology and Inflammation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9391044/ https://www.ncbi.nlm.nih.gov/pubmed/35950748 http://dx.doi.org/10.7554/eLife.74183 |
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