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Microbiota-Derived Extracellular Vesicles Promote Immunity and Intestinal Maturation in Suckling Rats

Microbiota–host communication is primarily achieved by secreted factors that can penetrate the mucosal surface, such as extracellular membrane vesicles (EVs). The EVs released by the gut microbiota have been extensively studied in cellular and experimental models of human diseases. However, little i...

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Autores principales: Martínez-Ruiz, Sergio, Sáez-Fuertes, Laura, Casanova-Crespo, Sergi, Rodríguez-Lagunas, María J., Pérez-Cano, Francisco J., Badia, Josefa, Baldoma, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10649425/
https://www.ncbi.nlm.nih.gov/pubmed/37960354
http://dx.doi.org/10.3390/nu15214701
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author Martínez-Ruiz, Sergio
Sáez-Fuertes, Laura
Casanova-Crespo, Sergi
Rodríguez-Lagunas, María J.
Pérez-Cano, Francisco J.
Badia, Josefa
Baldoma, Laura
author_facet Martínez-Ruiz, Sergio
Sáez-Fuertes, Laura
Casanova-Crespo, Sergi
Rodríguez-Lagunas, María J.
Pérez-Cano, Francisco J.
Badia, Josefa
Baldoma, Laura
author_sort Martínez-Ruiz, Sergio
collection PubMed
description Microbiota–host communication is primarily achieved by secreted factors that can penetrate the mucosal surface, such as extracellular membrane vesicles (EVs). The EVs released by the gut microbiota have been extensively studied in cellular and experimental models of human diseases. However, little is known about their in vivo effects in early life, specifically regarding immune and intestinal maturation. This study aimed to investigate the effects of daily administration of EVs from probiotic and commensal E. coli strains in healthy suckling rats during the first 16 days of life. On days 8 and 16, we assessed various intestinal and systemic variables in relation to animal growth, humoral and cellular immunity, epithelial barrier maturation, and intestinal architecture. On day 16, animals given probiotic/microbiota EVs exhibited higher levels of plasma IgG, IgA, and IgM and a greater proportion of Tc, NK, and NKT cells in the spleen. In the small intestine, EVs increased the villi area and modulated the expression of genes related to immune function, inflammation, and intestinal permeability, shifting towards an anti-inflammatory and barrier protective profile from day 8. In conclusion, interventions involving probiotic/microbiota EVs may represent a safe postbiotic strategy to stimulate immunity and intestinal maturation in early life.
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spelling pubmed-106494252023-11-06 Microbiota-Derived Extracellular Vesicles Promote Immunity and Intestinal Maturation in Suckling Rats Martínez-Ruiz, Sergio Sáez-Fuertes, Laura Casanova-Crespo, Sergi Rodríguez-Lagunas, María J. Pérez-Cano, Francisco J. Badia, Josefa Baldoma, Laura Nutrients Article Microbiota–host communication is primarily achieved by secreted factors that can penetrate the mucosal surface, such as extracellular membrane vesicles (EVs). The EVs released by the gut microbiota have been extensively studied in cellular and experimental models of human diseases. However, little is known about their in vivo effects in early life, specifically regarding immune and intestinal maturation. This study aimed to investigate the effects of daily administration of EVs from probiotic and commensal E. coli strains in healthy suckling rats during the first 16 days of life. On days 8 and 16, we assessed various intestinal and systemic variables in relation to animal growth, humoral and cellular immunity, epithelial barrier maturation, and intestinal architecture. On day 16, animals given probiotic/microbiota EVs exhibited higher levels of plasma IgG, IgA, and IgM and a greater proportion of Tc, NK, and NKT cells in the spleen. In the small intestine, EVs increased the villi area and modulated the expression of genes related to immune function, inflammation, and intestinal permeability, shifting towards an anti-inflammatory and barrier protective profile from day 8. In conclusion, interventions involving probiotic/microbiota EVs may represent a safe postbiotic strategy to stimulate immunity and intestinal maturation in early life. MDPI 2023-11-06 /pmc/articles/PMC10649425/ /pubmed/37960354 http://dx.doi.org/10.3390/nu15214701 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Martínez-Ruiz, Sergio
Sáez-Fuertes, Laura
Casanova-Crespo, Sergi
Rodríguez-Lagunas, María J.
Pérez-Cano, Francisco J.
Badia, Josefa
Baldoma, Laura
Microbiota-Derived Extracellular Vesicles Promote Immunity and Intestinal Maturation in Suckling Rats
title Microbiota-Derived Extracellular Vesicles Promote Immunity and Intestinal Maturation in Suckling Rats
title_full Microbiota-Derived Extracellular Vesicles Promote Immunity and Intestinal Maturation in Suckling Rats
title_fullStr Microbiota-Derived Extracellular Vesicles Promote Immunity and Intestinal Maturation in Suckling Rats
title_full_unstemmed Microbiota-Derived Extracellular Vesicles Promote Immunity and Intestinal Maturation in Suckling Rats
title_short Microbiota-Derived Extracellular Vesicles Promote Immunity and Intestinal Maturation in Suckling Rats
title_sort microbiota-derived extracellular vesicles promote immunity and intestinal maturation in suckling rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10649425/
https://www.ncbi.nlm.nih.gov/pubmed/37960354
http://dx.doi.org/10.3390/nu15214701
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