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Bovine milk exosomes affected proliferation of macrophages under hypoxia

Exosomes are extracellular vesicles implicated in cell-to-cell communication. The objective was to investigate the effect of exosomes in macrophages under hypoxia. Exosomes were isolated from skim milk using differential centrifugation and was characterized by particle size and exosomal markers TSG1...

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Autores principales: Matic, Svjetlana, Dia, Vermont P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641008/
https://www.ncbi.nlm.nih.gov/pubmed/36387601
http://dx.doi.org/10.1016/j.crfs.2022.11.002
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author Matic, Svjetlana
Dia, Vermont P.
author_facet Matic, Svjetlana
Dia, Vermont P.
author_sort Matic, Svjetlana
collection PubMed
description Exosomes are extracellular vesicles implicated in cell-to-cell communication. The objective was to investigate the effect of exosomes in macrophages under hypoxia. Exosomes were isolated from skim milk using differential centrifugation and was characterized by particle size and exosomal markers TSG101, CD81, and ALIX. The effect of exosomes on macrophages under hypoxia was investigated by assessing proliferation, cytokine and reactive oxygen species (ROS) production, and cell cycle. Exosomes treatment increased the cell viability under hypoxia while ROS production was significantly reduced. The production of TNF-α was not affected by hypoxia alone but increased in a dose-dependent manner in cells treated with exosomes under hypoxic condition. Hypoxia arrested cells in the G0/G1 phase whereas exosome treatment reduced the cell in this phase. Our study found that bovine milk exosomes affect the proliferation of macrophages under hypoxia and are able to reverse the adverse effects of hypoxia on cell viability.
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spelling pubmed-96410082022-11-15 Bovine milk exosomes affected proliferation of macrophages under hypoxia Matic, Svjetlana Dia, Vermont P. Curr Res Food Sci Short Communication Exosomes are extracellular vesicles implicated in cell-to-cell communication. The objective was to investigate the effect of exosomes in macrophages under hypoxia. Exosomes were isolated from skim milk using differential centrifugation and was characterized by particle size and exosomal markers TSG101, CD81, and ALIX. The effect of exosomes on macrophages under hypoxia was investigated by assessing proliferation, cytokine and reactive oxygen species (ROS) production, and cell cycle. Exosomes treatment increased the cell viability under hypoxia while ROS production was significantly reduced. The production of TNF-α was not affected by hypoxia alone but increased in a dose-dependent manner in cells treated with exosomes under hypoxic condition. Hypoxia arrested cells in the G0/G1 phase whereas exosome treatment reduced the cell in this phase. Our study found that bovine milk exosomes affect the proliferation of macrophages under hypoxia and are able to reverse the adverse effects of hypoxia on cell viability. Elsevier 2022-11-05 /pmc/articles/PMC9641008/ /pubmed/36387601 http://dx.doi.org/10.1016/j.crfs.2022.11.002 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Short Communication
Matic, Svjetlana
Dia, Vermont P.
Bovine milk exosomes affected proliferation of macrophages under hypoxia
title Bovine milk exosomes affected proliferation of macrophages under hypoxia
title_full Bovine milk exosomes affected proliferation of macrophages under hypoxia
title_fullStr Bovine milk exosomes affected proliferation of macrophages under hypoxia
title_full_unstemmed Bovine milk exosomes affected proliferation of macrophages under hypoxia
title_short Bovine milk exosomes affected proliferation of macrophages under hypoxia
title_sort bovine milk exosomes affected proliferation of macrophages under hypoxia
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641008/
https://www.ncbi.nlm.nih.gov/pubmed/36387601
http://dx.doi.org/10.1016/j.crfs.2022.11.002
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