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Effects of Milk-Derived Extracellular Vesicles on the Colonic Transcriptome and Proteome in Murine Model

Evidence shows that effective nutritional intervention can prevent or mitigate the risk and morbidity of inflammatory bowel disease (IBD). Bovine milk extracellular vesicles (mEVs), a major bioactive constituent of milk, play an important role in maintaining intestinal health. The aims of this study...

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Autores principales: Du, Chunmei, Zhao, Yiguang, Wang, Kun, Nan, Xuemei, Chen, Ruipeng, Xiong, Benhai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9332160/
https://www.ncbi.nlm.nih.gov/pubmed/35893911
http://dx.doi.org/10.3390/nu14153057
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author Du, Chunmei
Zhao, Yiguang
Wang, Kun
Nan, Xuemei
Chen, Ruipeng
Xiong, Benhai
author_facet Du, Chunmei
Zhao, Yiguang
Wang, Kun
Nan, Xuemei
Chen, Ruipeng
Xiong, Benhai
author_sort Du, Chunmei
collection PubMed
description Evidence shows that effective nutritional intervention can prevent or mitigate the risk and morbidity of inflammatory bowel disease (IBD). Bovine milk extracellular vesicles (mEVs), a major bioactive constituent of milk, play an important role in maintaining intestinal health. The aims of this study were to assess the effects of mEV pre-supplementation on the colonic transcriptome and proteome in dextran sulphate sodium (DSS)-induced acute colitis, in order to understand the underlying molecular mechanisms of mEV protection against acute colitis. Our results revealed that dietary mEV supplementation alleviated the severity of acute colitis, as evidenced by the reduced disease activity index scores, histological damage, and infiltration of inflammatory cells. In addition, transcriptome profiling analysis found that oral mEVs significantly reduced the expression of pro-inflammatory cytokines (IL-1β, IL-6, IL-17A and IL-33), chemokine ligands (CXCL1, CXCL2, CXCL3, CXCL5, CCL3 and CCL11) and chemokine receptors (CXCR2 and CCR3). Moreover, oral mEVs up-regulated 109 proteins and down-regulated 150 proteins in the DSS-induced murine model, which were involved in modulating amino acid metabolism and lipid metabolism. Collectively, this study might provide new insights for identifying potential targets for the therapeutic effects of mEVs on colitis.
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spelling pubmed-93321602022-07-29 Effects of Milk-Derived Extracellular Vesicles on the Colonic Transcriptome and Proteome in Murine Model Du, Chunmei Zhao, Yiguang Wang, Kun Nan, Xuemei Chen, Ruipeng Xiong, Benhai Nutrients Article Evidence shows that effective nutritional intervention can prevent or mitigate the risk and morbidity of inflammatory bowel disease (IBD). Bovine milk extracellular vesicles (mEVs), a major bioactive constituent of milk, play an important role in maintaining intestinal health. The aims of this study were to assess the effects of mEV pre-supplementation on the colonic transcriptome and proteome in dextran sulphate sodium (DSS)-induced acute colitis, in order to understand the underlying molecular mechanisms of mEV protection against acute colitis. Our results revealed that dietary mEV supplementation alleviated the severity of acute colitis, as evidenced by the reduced disease activity index scores, histological damage, and infiltration of inflammatory cells. In addition, transcriptome profiling analysis found that oral mEVs significantly reduced the expression of pro-inflammatory cytokines (IL-1β, IL-6, IL-17A and IL-33), chemokine ligands (CXCL1, CXCL2, CXCL3, CXCL5, CCL3 and CCL11) and chemokine receptors (CXCR2 and CCR3). Moreover, oral mEVs up-regulated 109 proteins and down-regulated 150 proteins in the DSS-induced murine model, which were involved in modulating amino acid metabolism and lipid metabolism. Collectively, this study might provide new insights for identifying potential targets for the therapeutic effects of mEVs on colitis. MDPI 2022-07-26 /pmc/articles/PMC9332160/ /pubmed/35893911 http://dx.doi.org/10.3390/nu14153057 Text en © 2022 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
Du, Chunmei
Zhao, Yiguang
Wang, Kun
Nan, Xuemei
Chen, Ruipeng
Xiong, Benhai
Effects of Milk-Derived Extracellular Vesicles on the Colonic Transcriptome and Proteome in Murine Model
title Effects of Milk-Derived Extracellular Vesicles on the Colonic Transcriptome and Proteome in Murine Model
title_full Effects of Milk-Derived Extracellular Vesicles on the Colonic Transcriptome and Proteome in Murine Model
title_fullStr Effects of Milk-Derived Extracellular Vesicles on the Colonic Transcriptome and Proteome in Murine Model
title_full_unstemmed Effects of Milk-Derived Extracellular Vesicles on the Colonic Transcriptome and Proteome in Murine Model
title_short Effects of Milk-Derived Extracellular Vesicles on the Colonic Transcriptome and Proteome in Murine Model
title_sort effects of milk-derived extracellular vesicles on the colonic transcriptome and proteome in murine model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9332160/
https://www.ncbi.nlm.nih.gov/pubmed/35893911
http://dx.doi.org/10.3390/nu14153057
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