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A genetically encoded sensor for visualizing leukotriene B4 gradients in vivo
Leukotriene B(4) (LTB(4)) is a potent lipid chemoattractant driving inflammatory responses during host defense, allergy, autoimmune and metabolic diseases. Gradients of LTB(4) orchestrate leukocyte recruitment and swarming to sites of tissue damage and infection. How LTB(4) gradients form and spread...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10393954/ https://www.ncbi.nlm.nih.gov/pubmed/37528073 http://dx.doi.org/10.1038/s41467-023-40326-6 |
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author | Tamás, Szimonetta Xénia Roux, Benoit Thomas Vámosi, Boldizsár Dehne, Fabian Gregor Török, Anna Fazekas, László Enyedi, Balázs |
author_facet | Tamás, Szimonetta Xénia Roux, Benoit Thomas Vámosi, Boldizsár Dehne, Fabian Gregor Török, Anna Fazekas, László Enyedi, Balázs |
author_sort | Tamás, Szimonetta Xénia |
collection | PubMed |
description | Leukotriene B(4) (LTB(4)) is a potent lipid chemoattractant driving inflammatory responses during host defense, allergy, autoimmune and metabolic diseases. Gradients of LTB(4) orchestrate leukocyte recruitment and swarming to sites of tissue damage and infection. How LTB(4) gradients form and spread in live tissues to regulate these processes remains largely elusive due to the lack of suitable tools for monitoring LTB(4) levels in vivo. Here, we develop GEM-LTB(4), a genetically encoded green fluorescent LTB(4) biosensor based on the human G-protein-coupled receptor BLT1. GEM-LTB(4) shows high sensitivity, specificity and a robust fluorescence increase in response to LTB(4) without affecting downstream signaling pathways. We use GEM-LTB(4) to measure ex vivo LTB(4) production of murine neutrophils. Transgenic expression of GEM-LTB(4) in zebrafish allows the real-time visualization of both exogenously applied and endogenously produced LTB(4) gradients. GEM-LTB(4) thus serves as a broadly applicable tool for analyzing LTB(4) dynamics in various experimental systems and model organisms. |
format | Online Article Text |
id | pubmed-10393954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103939542023-08-03 A genetically encoded sensor for visualizing leukotriene B4 gradients in vivo Tamás, Szimonetta Xénia Roux, Benoit Thomas Vámosi, Boldizsár Dehne, Fabian Gregor Török, Anna Fazekas, László Enyedi, Balázs Nat Commun Article Leukotriene B(4) (LTB(4)) is a potent lipid chemoattractant driving inflammatory responses during host defense, allergy, autoimmune and metabolic diseases. Gradients of LTB(4) orchestrate leukocyte recruitment and swarming to sites of tissue damage and infection. How LTB(4) gradients form and spread in live tissues to regulate these processes remains largely elusive due to the lack of suitable tools for monitoring LTB(4) levels in vivo. Here, we develop GEM-LTB(4), a genetically encoded green fluorescent LTB(4) biosensor based on the human G-protein-coupled receptor BLT1. GEM-LTB(4) shows high sensitivity, specificity and a robust fluorescence increase in response to LTB(4) without affecting downstream signaling pathways. We use GEM-LTB(4) to measure ex vivo LTB(4) production of murine neutrophils. Transgenic expression of GEM-LTB(4) in zebrafish allows the real-time visualization of both exogenously applied and endogenously produced LTB(4) gradients. GEM-LTB(4) thus serves as a broadly applicable tool for analyzing LTB(4) dynamics in various experimental systems and model organisms. Nature Publishing Group UK 2023-08-01 /pmc/articles/PMC10393954/ /pubmed/37528073 http://dx.doi.org/10.1038/s41467-023-40326-6 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 | Article Tamás, Szimonetta Xénia Roux, Benoit Thomas Vámosi, Boldizsár Dehne, Fabian Gregor Török, Anna Fazekas, László Enyedi, Balázs A genetically encoded sensor for visualizing leukotriene B4 gradients in vivo |
title | A genetically encoded sensor for visualizing leukotriene B4 gradients in vivo |
title_full | A genetically encoded sensor for visualizing leukotriene B4 gradients in vivo |
title_fullStr | A genetically encoded sensor for visualizing leukotriene B4 gradients in vivo |
title_full_unstemmed | A genetically encoded sensor for visualizing leukotriene B4 gradients in vivo |
title_short | A genetically encoded sensor for visualizing leukotriene B4 gradients in vivo |
title_sort | genetically encoded sensor for visualizing leukotriene b4 gradients in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10393954/ https://www.ncbi.nlm.nih.gov/pubmed/37528073 http://dx.doi.org/10.1038/s41467-023-40326-6 |
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