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Updated: Aug 7, 2025

Purification and microRNA Profiling of Exosomes Derived from Blood and Culture Media
Published on: June 14, 2013
Cooked pork-derived exosome nanovesicles mediate metabolic disorder-microRNA could be the culprit
Linyuan Shen1,2, Jianfeng Ma1,2, Yiting Yang1,2
1Farm Animal Genetic Resource Exploration and Innovation Key Laboratory of Sichuan Province, Sichuan Agricultural University, Chengdu, 611130, China.
Abstract:
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.
Insights
Exosomes from cooked pork, containing specific microRNAs, were given to mice. This led to abnormal glucose metabolism and insulin resistance, suggesting dietary microRNAs can impact metabolic health.
Area of Science:
- Biochemistry
- Molecular Biology
- Metabolomics
Background:
- Exosomes are nanoscale vesicles involved in intercellular communication.
- Dietary components can influence host physiology through various mechanisms.
- MicroRNAs (miRNAs) within exosomes are potential bioactive molecules.
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