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Lipopolysaccharide Administration Alters Extracellular Vesicles in Cell Lines and Mice

Extracellular vesicles (EVs) play a fundamental role in cell and infection biology and have the potential to act as biomarkers for novel diagnostic tools. In this study, we explored the in vitro impact of bacterial lipopolysaccharide administration on cell lines that represents a target for bacteria...

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Autores principales: Jones, Leandra B., Kumar, Sanjay, Bell, Courtnee’ R., Crenshaw, Brennetta J., Coats, Mamie T., Sims, Brian, Matthews, Qiana L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952295/
https://www.ncbi.nlm.nih.gov/pubmed/33559732
http://dx.doi.org/10.1007/s00284-021-02348-5
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author Jones, Leandra B.
Kumar, Sanjay
Bell, Courtnee’ R.
Crenshaw, Brennetta J.
Coats, Mamie T.
Sims, Brian
Matthews, Qiana L.
author_facet Jones, Leandra B.
Kumar, Sanjay
Bell, Courtnee’ R.
Crenshaw, Brennetta J.
Coats, Mamie T.
Sims, Brian
Matthews, Qiana L.
author_sort Jones, Leandra B.
collection PubMed
description Extracellular vesicles (EVs) play a fundamental role in cell and infection biology and have the potential to act as biomarkers for novel diagnostic tools. In this study, we explored the in vitro impact of bacterial lipopolysaccharide administration on cell lines that represents a target for bacterial infection in the host. Administration of lipopolysaccharide at varying concentrations to A549 and BV-2 cell lines caused only modest changes in cell death, but EV numbers were significantly changed. After treatment with the highest concentration of lipopolysaccharide, EVs derived from A549 cells packaged significantly less interleukin-6 and lysosomal-associated membrane protein 1. EVs derived from BV-2 cells packaged significantly less tumor necrosis factor after administration of lipopolysaccharide concentrations of 0.1 µg/mL and 1 µg/mL. We also examined the impact of lipopolysaccharide administration on exosome biogenesis and cargo composition in BALB/c mice. Serum-isolated EVs from lipopolysaccharide-treated mice showed significantly increased lysosomal-associated membrane protein 1 and toll-like receptor 4 levels compared with EVs from control mice. In summary, this study demonstrated that EV numbers and cargo were altered using these in vitro and in vivo models of bacterial infection. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00284-021-02348-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-79522952021-03-28 Lipopolysaccharide Administration Alters Extracellular Vesicles in Cell Lines and Mice Jones, Leandra B. Kumar, Sanjay Bell, Courtnee’ R. Crenshaw, Brennetta J. Coats, Mamie T. Sims, Brian Matthews, Qiana L. Curr Microbiol Article Extracellular vesicles (EVs) play a fundamental role in cell and infection biology and have the potential to act as biomarkers for novel diagnostic tools. In this study, we explored the in vitro impact of bacterial lipopolysaccharide administration on cell lines that represents a target for bacterial infection in the host. Administration of lipopolysaccharide at varying concentrations to A549 and BV-2 cell lines caused only modest changes in cell death, but EV numbers were significantly changed. After treatment with the highest concentration of lipopolysaccharide, EVs derived from A549 cells packaged significantly less interleukin-6 and lysosomal-associated membrane protein 1. EVs derived from BV-2 cells packaged significantly less tumor necrosis factor after administration of lipopolysaccharide concentrations of 0.1 µg/mL and 1 µg/mL. We also examined the impact of lipopolysaccharide administration on exosome biogenesis and cargo composition in BALB/c mice. Serum-isolated EVs from lipopolysaccharide-treated mice showed significantly increased lysosomal-associated membrane protein 1 and toll-like receptor 4 levels compared with EVs from control mice. In summary, this study demonstrated that EV numbers and cargo were altered using these in vitro and in vivo models of bacterial infection. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00284-021-02348-5) contains supplementary material, which is available to authorized users. Springer US 2021-02-09 2021 /pmc/articles/PMC7952295/ /pubmed/33559732 http://dx.doi.org/10.1007/s00284-021-02348-5 Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Jones, Leandra B.
Kumar, Sanjay
Bell, Courtnee’ R.
Crenshaw, Brennetta J.
Coats, Mamie T.
Sims, Brian
Matthews, Qiana L.
Lipopolysaccharide Administration Alters Extracellular Vesicles in Cell Lines and Mice
title Lipopolysaccharide Administration Alters Extracellular Vesicles in Cell Lines and Mice
title_full Lipopolysaccharide Administration Alters Extracellular Vesicles in Cell Lines and Mice
title_fullStr Lipopolysaccharide Administration Alters Extracellular Vesicles in Cell Lines and Mice
title_full_unstemmed Lipopolysaccharide Administration Alters Extracellular Vesicles in Cell Lines and Mice
title_short Lipopolysaccharide Administration Alters Extracellular Vesicles in Cell Lines and Mice
title_sort lipopolysaccharide administration alters extracellular vesicles in cell lines and mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952295/
https://www.ncbi.nlm.nih.gov/pubmed/33559732
http://dx.doi.org/10.1007/s00284-021-02348-5
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