# Sequencing and bioinformatics analysis of exosome-derived miRNAs in mouse models of pancreatic injury induced by OSA

## TL;DR

This study explores how exosomal miRNAs in mouse pancreatic tissue are affected by OSA-induced injury, offering new insights into OSA-related diabetes.

## Contribution

The first comprehensive analysis of exosome-derived miRNA expression in OSA-induced pancreatic injury in mice.

## Key findings

- 55 new and 277 existing miRNAs were identified in pancreatic exosomes from OSA-induced injury models.
- 33 downregulated and 3 upregulated miRNAs were found to be differentially expressed.
- GO and KEGG analyses revealed potential target genes and pathways linked to pancreatic injury.

## Abstract

The role of exosomal miRNAs involved in the pathogenesis and development of pancreatic injury caused by obstructive sleep apnea (OSA) remains unclear. Here, miRNA sequencing (miRNA-seq) was used to investigate the expression profile of exosomal miRNAs in pancreatic tissue in a mouse model of chronic intermittent hypoxia (CIH) -induced pancreatic injury.

Firstly, exosomes were isolated from pancreatic tissues of mice subjected to chronic intermittent hypoxia (CIH) or control conditions. Then, miRNA sequencing was performed, and differential expression analysis identified DE miRNAs. The potential functions of target genes were predicted by GO and KEGG analyses. Finally, a ceRNA interaction network was constructed to illustrate the relationships between miRNAs and targeted mRNAs.

A total of 55 newly predicted miRNAs and 277 existing miRNAs were identified in pancreatic tissue exosomes from the mouse model of chronic intermittent hypoxic-induced pancreatic injury. 3 upregulated and 33 downregulated miRNAs with differential expression were identified. 8 exosome-derived miRNAs were selected to construct CNC networks to predict target genes. Some targets and pathways were elucidated by GO analysis and KEGG analysis.

Our work first comprehensively studied the expression profile of exosome-derived miRNA in pancreatic tissue of mouse models of OSA-induced pancreatic injury, bringing fresh perspectives on managing diabetes mellitus brought on by OSA.