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Extracellular vesicles derived from small intestinal lamina propria reduce antigen-specific immune response
BACKGROUND/AIMS: Extracellular vesicles (EVs) are secreted from various types of cells and have specific functions related to their origin. EVs are observed in the small intestinal lamina propria (lpEVs), but their function remains unclear. This study aimed to investigate the role of lpEVs. METHODS:...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association of Internal Medicine
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8747917/ https://www.ncbi.nlm.nih.gov/pubmed/34425655 http://dx.doi.org/10.3904/kjim.2020.510 |
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author | Shin, Tae-Seop Park, Jae Yong Kim, Yoon-Keun Kim, Jae Gyu |
author_facet | Shin, Tae-Seop Park, Jae Yong Kim, Yoon-Keun Kim, Jae Gyu |
author_sort | Shin, Tae-Seop |
collection | PubMed |
description | BACKGROUND/AIMS: Extracellular vesicles (EVs) are secreted from various types of cells and have specific functions related to their origin. EVs are observed in the small intestinal lamina propria (lpEVs), but their function remains unclear. This study aimed to investigate the role of lpEVs. METHODS: LpEVs were isolated from antigen (ovalbumin [OVA])-fed mice (lpEVs/OVA), and administrated to the naïve mice for 5 days before induction of lung inflammation. Afterwards, the mice were sensitized and challenged with OVA to evaluate the role of lpEVs/OVA in the regulation of immune tolerance. RESULTS: The isolated lpEVs/OVA were sphere-shaped, bi-layered vesicles of approximately 50 to 100 nm in size. The vesicles expressed CD81, A33 antigen, and major histocompatibility complex (MHC) class II on the surface. When administrated to naïve mice, the lpEVs/OVA migrated to the spleen. Intraperitoneal lpEVs/OVA administration to naïve mice decreased the immune response against sensitized antigen in a CD4(+)FoxP3(+)T cell-dependent manner. CONCLUSIONS: EVs are actively secreted from small intestinal epithelial cells to deliver information about orally administered antigens to immune cells, which will facilitate the modulation of the immune response by acting as an intercellular communicasome. |
format | Online Article Text |
id | pubmed-8747917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Korean Association of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-87479172022-01-18 Extracellular vesicles derived from small intestinal lamina propria reduce antigen-specific immune response Shin, Tae-Seop Park, Jae Yong Kim, Yoon-Keun Kim, Jae Gyu Korean J Intern Med Original Article BACKGROUND/AIMS: Extracellular vesicles (EVs) are secreted from various types of cells and have specific functions related to their origin. EVs are observed in the small intestinal lamina propria (lpEVs), but their function remains unclear. This study aimed to investigate the role of lpEVs. METHODS: LpEVs were isolated from antigen (ovalbumin [OVA])-fed mice (lpEVs/OVA), and administrated to the naïve mice for 5 days before induction of lung inflammation. Afterwards, the mice were sensitized and challenged with OVA to evaluate the role of lpEVs/OVA in the regulation of immune tolerance. RESULTS: The isolated lpEVs/OVA were sphere-shaped, bi-layered vesicles of approximately 50 to 100 nm in size. The vesicles expressed CD81, A33 antigen, and major histocompatibility complex (MHC) class II on the surface. When administrated to naïve mice, the lpEVs/OVA migrated to the spleen. Intraperitoneal lpEVs/OVA administration to naïve mice decreased the immune response against sensitized antigen in a CD4(+)FoxP3(+)T cell-dependent manner. CONCLUSIONS: EVs are actively secreted from small intestinal epithelial cells to deliver information about orally administered antigens to immune cells, which will facilitate the modulation of the immune response by acting as an intercellular communicasome. Korean Association of Internal Medicine 2022-01 2021-08-25 /pmc/articles/PMC8747917/ /pubmed/34425655 http://dx.doi.org/10.3904/kjim.2020.510 Text en Copyright © 2022 The Korean Association of Internal Medicine https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Shin, Tae-Seop Park, Jae Yong Kim, Yoon-Keun Kim, Jae Gyu Extracellular vesicles derived from small intestinal lamina propria reduce antigen-specific immune response |
title | Extracellular vesicles derived from small intestinal lamina propria reduce antigen-specific immune response |
title_full | Extracellular vesicles derived from small intestinal lamina propria reduce antigen-specific immune response |
title_fullStr | Extracellular vesicles derived from small intestinal lamina propria reduce antigen-specific immune response |
title_full_unstemmed | Extracellular vesicles derived from small intestinal lamina propria reduce antigen-specific immune response |
title_short | Extracellular vesicles derived from small intestinal lamina propria reduce antigen-specific immune response |
title_sort | extracellular vesicles derived from small intestinal lamina propria reduce antigen-specific immune response |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8747917/ https://www.ncbi.nlm.nih.gov/pubmed/34425655 http://dx.doi.org/10.3904/kjim.2020.510 |
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