Porcine milk small extracellular vesicles modulate peripheral blood mononuclear cell proteome in vitro

Small extracellular vesicles (EVs) are a subtype of nano-sized extracellular vesicles that mediate intercellular communication. EVs can be found in different body fluids, including milk. Monocytes internalize porcine milk EVs and modulate immune functions in vitro by decreasing their phagocytosis and chemotaxis while increasing their oxidative burst. This study aimed to assess the impact of porcine milk EVs on the porcine peripheral blood mononuclear cells (PBMC) proteome. Porcine PBMC were incubated with porcine milk EVs or medium as a control. Extracted proteins were then analyzed using nano-LC-MS/MS. A total of 1584 proteins were identified. The supervised multivariate statistical analysis, sparse variant partial least squares - discriminant analysis (sPLS-DA) for paired data identified discriminant proteins (DP) that contributed to a clear separation between the porcine milk EVs treated cells and control groups. A total of 384 DP from both components were selected. Gene Ontology (GO) enrichment analysis with ProteINSIDE provided the evidence that the DP with a higher abundance in porcine milk EVs, like TLR2, APOE, CD36, MFGE8, were mainly involved in innate immunity and the process of EVs uptake processes. These results provide a proteomics background to the immunomodulatory activity of porcine milk EVs and to the potential mechanisms used by immune cells to internalize them.

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Publication Details

Journal
Scientific Reports
Published
2025-03-07
DOI
https://doi.org/10.1038/s41598-025-92550-3
Citations
2
Primary Topic
Extracellular vesicles in disease
Type
article
Field-Weighted Citation Impact
1.61
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article

Porcine milk small extracellular vesicles modulate peripheral blood mononuclear cell proteome in vitro

A. Agazzi, Muriel Bonnet, Cristina Lecchi, Fabrizio Ceciliani et al.
2 citations
Scientific Reports
Extracellular vesicles in disease
1.61
article

Porcine milk small extracellular vesicles modulate peripheral blood mononuclear cell proteome in vitro

A. Agazzi, Muriel Bonnet, Cristina Lecchi, Fabrizio Ceciliani, Gabriela Ávila, Didier Viala, Sebastian Dejean
article en
2 citations

Abstract

Small extracellular vesicles (EVs) are a subtype of nano-sized extracellular vesicles that mediate intercellular communication. EVs can be found in different body fluids, including milk. Monocytes internalize porcine milk EVs and modulate immune functions in vitro by decreasing their phagocytosis and chemotaxis while increasing their oxidative burst. This study aimed to assess the impact of porcine milk EVs on the porcine peripheral blood mononuclear cells (PBMC) proteome. Porcine PBMC were incubated with porcine milk EVs or medium as a control. Extracted proteins were then analyzed using nano-LC-MS/MS. A total of 1584 proteins were identified. The supervised multivariate statistical analysis, sparse variant partial least squares - discriminant analysis (sPLS-DA) for paired data identified discriminant proteins (DP) that contributed to a clear separation between the porcine milk EVs treated cells and control groups. A total of 384 DP from both components were selected. Gene Ontology (GO) enrichment analysis with ProteINSIDE provided the evidence that the DP with a higher abundance in porcine milk EVs, like TLR2, APOE, CD36, MFGE8, were mainly involved in innate immunity and the process of EVs uptake processes. These results provide a proteomics background to the immunomodulatory activity of porcine milk EVs and to the potential mechanisms used by immune cells to internalize them.

Scientific ReportsVol. 15(1)
Centre National de la Recherche Scientifique (FR), Atomic Minerals Directorate for Exploration and Research (IN), Université Toulouse III - Paul Sabatier (FR), University of Milan (IT), Université Clermont Auvergne (FR), Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR), VetAgro Sup (FR), Institut de Mathématiques de Toulouse (FR)
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Openalex Percentile: Top 19%
Extracellular vesicles in disease
1.61
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