Cargando…
Transcellular biosynthesis of leukotriene B(4) orchestrates neutrophil swarming to fungi
Neutrophil swarming is an emergent host defense mechanism triggered by targets larger than a single neutrophil’s capacity to phagocytose. Swarming synergizes neutrophil functions, including chemotaxis, phagocytosis, and reactive oxygen species (ROS) production, and coordinates their deployment by ma...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9576560/ https://www.ncbi.nlm.nih.gov/pubmed/36267914 http://dx.doi.org/10.1016/j.isci.2022.105226 |
_version_ | 1784811557861982208 |
---|---|
author | Hopke, Alex Lin, Tian Scherer, Allison K. Shay, Ashley E. Timmer, Kyle D. Wilson-Mifsud, Brittany Mansour, Michael K. Serhan, Charles N. Irimia, Daniel Hurley, Bryan P. |
author_facet | Hopke, Alex Lin, Tian Scherer, Allison K. Shay, Ashley E. Timmer, Kyle D. Wilson-Mifsud, Brittany Mansour, Michael K. Serhan, Charles N. Irimia, Daniel Hurley, Bryan P. |
author_sort | Hopke, Alex |
collection | PubMed |
description | Neutrophil swarming is an emergent host defense mechanism triggered by targets larger than a single neutrophil’s capacity to phagocytose. Swarming synergizes neutrophil functions, including chemotaxis, phagocytosis, and reactive oxygen species (ROS) production, and coordinates their deployment by many interacting neutrophils. The potent inflammatory lipid mediator leukotriene B(4) (LTB(4)) has been established as central to orchestrating neutrophil activities during swarming. However, the details regarding how this eicosanoid choreographs the neutrophils involved in swarming are not well explained. Here we leverage microfluidics, genetically deficient mouse cells, and targeted metabolipidomic analysis to demonstrate that transcellular biosynthesis occurs among neutrophils to generate LTB(4). Furthermore, transcellular biosynthesis is an entirely sufficient means of generating LTB(4) for the purposes of orchestrating neutrophil swarming. These results further our understanding of how neutrophils coordinate their activities during swarming, which will be critical in the design of eventual therapies that can harness the power of swarming behavior. |
format | Online Article Text |
id | pubmed-9576560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-95765602022-10-19 Transcellular biosynthesis of leukotriene B(4) orchestrates neutrophil swarming to fungi Hopke, Alex Lin, Tian Scherer, Allison K. Shay, Ashley E. Timmer, Kyle D. Wilson-Mifsud, Brittany Mansour, Michael K. Serhan, Charles N. Irimia, Daniel Hurley, Bryan P. iScience Article Neutrophil swarming is an emergent host defense mechanism triggered by targets larger than a single neutrophil’s capacity to phagocytose. Swarming synergizes neutrophil functions, including chemotaxis, phagocytosis, and reactive oxygen species (ROS) production, and coordinates their deployment by many interacting neutrophils. The potent inflammatory lipid mediator leukotriene B(4) (LTB(4)) has been established as central to orchestrating neutrophil activities during swarming. However, the details regarding how this eicosanoid choreographs the neutrophils involved in swarming are not well explained. Here we leverage microfluidics, genetically deficient mouse cells, and targeted metabolipidomic analysis to demonstrate that transcellular biosynthesis occurs among neutrophils to generate LTB(4). Furthermore, transcellular biosynthesis is an entirely sufficient means of generating LTB(4) for the purposes of orchestrating neutrophil swarming. These results further our understanding of how neutrophils coordinate their activities during swarming, which will be critical in the design of eventual therapies that can harness the power of swarming behavior. Elsevier 2022-09-28 /pmc/articles/PMC9576560/ /pubmed/36267914 http://dx.doi.org/10.1016/j.isci.2022.105226 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hopke, Alex Lin, Tian Scherer, Allison K. Shay, Ashley E. Timmer, Kyle D. Wilson-Mifsud, Brittany Mansour, Michael K. Serhan, Charles N. Irimia, Daniel Hurley, Bryan P. Transcellular biosynthesis of leukotriene B(4) orchestrates neutrophil swarming to fungi |
title | Transcellular biosynthesis of leukotriene B(4) orchestrates neutrophil swarming to fungi |
title_full | Transcellular biosynthesis of leukotriene B(4) orchestrates neutrophil swarming to fungi |
title_fullStr | Transcellular biosynthesis of leukotriene B(4) orchestrates neutrophil swarming to fungi |
title_full_unstemmed | Transcellular biosynthesis of leukotriene B(4) orchestrates neutrophil swarming to fungi |
title_short | Transcellular biosynthesis of leukotriene B(4) orchestrates neutrophil swarming to fungi |
title_sort | transcellular biosynthesis of leukotriene b(4) orchestrates neutrophil swarming to fungi |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9576560/ https://www.ncbi.nlm.nih.gov/pubmed/36267914 http://dx.doi.org/10.1016/j.isci.2022.105226 |
work_keys_str_mv | AT hopkealex transcellularbiosynthesisofleukotrieneb4orchestratesneutrophilswarmingtofungi AT lintian transcellularbiosynthesisofleukotrieneb4orchestratesneutrophilswarmingtofungi AT schererallisonk transcellularbiosynthesisofleukotrieneb4orchestratesneutrophilswarmingtofungi AT shayashleye transcellularbiosynthesisofleukotrieneb4orchestratesneutrophilswarmingtofungi AT timmerkyled transcellularbiosynthesisofleukotrieneb4orchestratesneutrophilswarmingtofungi AT wilsonmifsudbrittany transcellularbiosynthesisofleukotrieneb4orchestratesneutrophilswarmingtofungi AT mansourmichaelk transcellularbiosynthesisofleukotrieneb4orchestratesneutrophilswarmingtofungi AT serhancharlesn transcellularbiosynthesisofleukotrieneb4orchestratesneutrophilswarmingtofungi AT irimiadaniel transcellularbiosynthesisofleukotrieneb4orchestratesneutrophilswarmingtofungi AT hurleybryanp transcellularbiosynthesisofleukotrieneb4orchestratesneutrophilswarmingtofungi |