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Cooked pork-derived exosome nanovesicles mediate metabolic disorder—microRNA could be the culprit

In this study, exosomes from cooked meat were extracted by ultra-high-speed centrifugation. Approximately 80% of exosome vesicles were within 20–200 nm. In addition, the surface biomarkers of isolated exosomes were evaluated using flow cytometry. Further studies showed the exosomal microRNA profiles...

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Autores principales: Shen, Linyuan, Ma, Jianfeng, Yang, Yiting, Liao, Tianci, Wang, Jinyong, Chen, Lei, Zhang, Shunhua, Zhao, Ye, Niu, Lili, Hao, Xiaoxia, Jiang, Anan, Li, Xuewei, Gan, Mailin, Zhu, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9999493/
https://www.ncbi.nlm.nih.gov/pubmed/36894941
http://dx.doi.org/10.1186/s12951-023-01837-y
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author Shen, Linyuan
Ma, Jianfeng
Yang, Yiting
Liao, Tianci
Wang, Jinyong
Chen, Lei
Zhang, Shunhua
Zhao, Ye
Niu, Lili
Hao, Xiaoxia
Jiang, Anan
Li, Xuewei
Gan, Mailin
Zhu, Li
author_facet Shen, Linyuan
Ma, Jianfeng
Yang, Yiting
Liao, Tianci
Wang, Jinyong
Chen, Lei
Zhang, Shunhua
Zhao, Ye
Niu, Lili
Hao, Xiaoxia
Jiang, Anan
Li, Xuewei
Gan, Mailin
Zhu, Li
author_sort Shen, Linyuan
collection PubMed
description In this study, exosomes from cooked meat were extracted by ultra-high-speed centrifugation. Approximately 80% of exosome vesicles were within 20–200 nm. In addition, the surface biomarkers of isolated exosomes were evaluated using flow cytometry. Further studies showed the exosomal microRNA profiles were different among cooked porcine muscle, fat and liver. Cooked pork-derived exosomes were chronically administered to ICR mice by drinking for 80 days. The mice plasma levels of miR-1, miR-133a-3p, miR-206 and miR-99a were increased to varying degrees after drinking exosome enriched water. Furthermore, GTT and ITT results confirmed an abnormal glucose metabolism and insulin resistance in mice. Moreover, the lipid droplets were significantly increased in the mice liver. A transcriptome analysis performed with mice liver samples identified 446 differentially expressed genes (DEGs). Functional enrichment analysis found that DEGs were enriched in metabolic pathways. Overall, the results suggest that microRNAs derived form cooked pork may function as a critical regulator of metabolic disorder in mice.
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spelling pubmed-99994932023-03-11 Cooked pork-derived exosome nanovesicles mediate metabolic disorder—microRNA could be the culprit Shen, Linyuan Ma, Jianfeng Yang, Yiting Liao, Tianci Wang, Jinyong Chen, Lei Zhang, Shunhua Zhao, Ye Niu, Lili Hao, Xiaoxia Jiang, Anan Li, Xuewei Gan, Mailin Zhu, Li J Nanobiotechnology Correspondence In this study, exosomes from cooked meat were extracted by ultra-high-speed centrifugation. Approximately 80% of exosome vesicles were within 20–200 nm. In addition, the surface biomarkers of isolated exosomes were evaluated using flow cytometry. Further studies showed the exosomal microRNA profiles were different among cooked porcine muscle, fat and liver. Cooked pork-derived exosomes were chronically administered to ICR mice by drinking for 80 days. The mice plasma levels of miR-1, miR-133a-3p, miR-206 and miR-99a were increased to varying degrees after drinking exosome enriched water. Furthermore, GTT and ITT results confirmed an abnormal glucose metabolism and insulin resistance in mice. Moreover, the lipid droplets were significantly increased in the mice liver. A transcriptome analysis performed with mice liver samples identified 446 differentially expressed genes (DEGs). Functional enrichment analysis found that DEGs were enriched in metabolic pathways. Overall, the results suggest that microRNAs derived form cooked pork may function as a critical regulator of metabolic disorder in mice. BioMed Central 2023-03-09 /pmc/articles/PMC9999493/ /pubmed/36894941 http://dx.doi.org/10.1186/s12951-023-01837-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Correspondence
Shen, Linyuan
Ma, Jianfeng
Yang, Yiting
Liao, Tianci
Wang, Jinyong
Chen, Lei
Zhang, Shunhua
Zhao, Ye
Niu, Lili
Hao, Xiaoxia
Jiang, Anan
Li, Xuewei
Gan, Mailin
Zhu, Li
Cooked pork-derived exosome nanovesicles mediate metabolic disorder—microRNA could be the culprit
title Cooked pork-derived exosome nanovesicles mediate metabolic disorder—microRNA could be the culprit
title_full Cooked pork-derived exosome nanovesicles mediate metabolic disorder—microRNA could be the culprit
title_fullStr Cooked pork-derived exosome nanovesicles mediate metabolic disorder—microRNA could be the culprit
title_full_unstemmed Cooked pork-derived exosome nanovesicles mediate metabolic disorder—microRNA could be the culprit
title_short Cooked pork-derived exosome nanovesicles mediate metabolic disorder—microRNA could be the culprit
title_sort cooked pork-derived exosome nanovesicles mediate metabolic disorder—microrna could be the culprit
topic Correspondence
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9999493/
https://www.ncbi.nlm.nih.gov/pubmed/36894941
http://dx.doi.org/10.1186/s12951-023-01837-y
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