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Graphene oxide elicits microbiome-dependent type 2 immune responses via the aryl hydrocarbon receptor
The gut microbiome produces metabolites that interact with the aryl hydrocarbon receptor (AhR), a key regulator of immune homoeostasis in the gut(1,2). Here we show that oral exposure to graphene oxide (GO) modulates the composition of the gut microbiome in adult zebrafish, with significant differen...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9879769/ https://www.ncbi.nlm.nih.gov/pubmed/36509925 http://dx.doi.org/10.1038/s41565-022-01260-8 |
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author | Peng, Guotao Sinkko, Hanna M. Alenius, Harri Lozano, Neus Kostarelos, Kostas Bräutigam, Lars Fadeel, Bengt |
author_facet | Peng, Guotao Sinkko, Hanna M. Alenius, Harri Lozano, Neus Kostarelos, Kostas Bräutigam, Lars Fadeel, Bengt |
author_sort | Peng, Guotao |
collection | PubMed |
description | The gut microbiome produces metabolites that interact with the aryl hydrocarbon receptor (AhR), a key regulator of immune homoeostasis in the gut(1,2). Here we show that oral exposure to graphene oxide (GO) modulates the composition of the gut microbiome in adult zebrafish, with significant differences in wild-type versus ahr2-deficient animals. Furthermore, GO was found to elicit AhR-dependent induction of cyp1a and homing of lck(+) cells to the gut in germ-free zebrafish larvae when combined with the short-chain fatty acid butyrate. To obtain further insights into the immune responses to GO, we used single-cell RNA sequencing to profile cells from whole germ-free embryos as well as cells enriched for lck. These studies provided evidence for the existence of innate lymphoid cell (ILC)-like cells(3) in germ-free zebrafish. Moreover, GO endowed with a ‘corona’ of microbial butyrate triggered the induction of ILC2-like cells with attributes of regulatory cells. Taken together, this study shows that a nanomaterial can influence the crosstalk between the microbiome and immune system in an AhR-dependent manner. |
format | Online Article Text |
id | pubmed-9879769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98797692023-01-28 Graphene oxide elicits microbiome-dependent type 2 immune responses via the aryl hydrocarbon receptor Peng, Guotao Sinkko, Hanna M. Alenius, Harri Lozano, Neus Kostarelos, Kostas Bräutigam, Lars Fadeel, Bengt Nat Nanotechnol Letter The gut microbiome produces metabolites that interact with the aryl hydrocarbon receptor (AhR), a key regulator of immune homoeostasis in the gut(1,2). Here we show that oral exposure to graphene oxide (GO) modulates the composition of the gut microbiome in adult zebrafish, with significant differences in wild-type versus ahr2-deficient animals. Furthermore, GO was found to elicit AhR-dependent induction of cyp1a and homing of lck(+) cells to the gut in germ-free zebrafish larvae when combined with the short-chain fatty acid butyrate. To obtain further insights into the immune responses to GO, we used single-cell RNA sequencing to profile cells from whole germ-free embryos as well as cells enriched for lck. These studies provided evidence for the existence of innate lymphoid cell (ILC)-like cells(3) in germ-free zebrafish. Moreover, GO endowed with a ‘corona’ of microbial butyrate triggered the induction of ILC2-like cells with attributes of regulatory cells. Taken together, this study shows that a nanomaterial can influence the crosstalk between the microbiome and immune system in an AhR-dependent manner. Nature Publishing Group UK 2022-12-12 2023 /pmc/articles/PMC9879769/ /pubmed/36509925 http://dx.doi.org/10.1038/s41565-022-01260-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Letter Peng, Guotao Sinkko, Hanna M. Alenius, Harri Lozano, Neus Kostarelos, Kostas Bräutigam, Lars Fadeel, Bengt Graphene oxide elicits microbiome-dependent type 2 immune responses via the aryl hydrocarbon receptor |
title | Graphene oxide elicits microbiome-dependent type 2 immune responses via the aryl hydrocarbon receptor |
title_full | Graphene oxide elicits microbiome-dependent type 2 immune responses via the aryl hydrocarbon receptor |
title_fullStr | Graphene oxide elicits microbiome-dependent type 2 immune responses via the aryl hydrocarbon receptor |
title_full_unstemmed | Graphene oxide elicits microbiome-dependent type 2 immune responses via the aryl hydrocarbon receptor |
title_short | Graphene oxide elicits microbiome-dependent type 2 immune responses via the aryl hydrocarbon receptor |
title_sort | graphene oxide elicits microbiome-dependent type 2 immune responses via the aryl hydrocarbon receptor |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9879769/ https://www.ncbi.nlm.nih.gov/pubmed/36509925 http://dx.doi.org/10.1038/s41565-022-01260-8 |
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