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Bone marrow mesenchymal stem cell-derived exosomes alleviate hyperoxia-induced lung injury via the manipulation of microRNA-425
- Source :
- Archives of biochemistry and biophysics. 697
- Publication Year :
- 2020
-
Abstract
- Background Hyperoxia-induced lung injury (HILI) is an acute lung injury (LI) induced by extended periods of exposure to hyperoxia. Alleviating LI by bone marrow mesenchymal stem cell-derived exosomes (BMSCs-Exos) and microRNAs (miRs) has been previously reported. This study is devised to probe the interaction between BMSCs-Exos and miR-425 in HILI. Methods Firstly, BMSCs-Exos were isolated and identified. Then, HILI rat models and RLE-6TN cell models were successfully established and treated by BMSCs-Exos. Afterwards, functional assays were conducted to explore cell biological behaviors in models, with miR-425 expression detected. Then, the target relation between miR-425 and PTEN was clarified by luciferase reporter assay. Eventually, expression of PTEN and the PI3K/Akt axis was assessed by Western blotting and qRT-PCR. Results BMSCs-Exos promoted miR-425 expression and attenuated HILI and H2O2 induced RLE-6TN cell injury as evidence by alleviated lung cell injury, decreased TUNEL-positive cells, induced cell viability and declined apoptosis (all p Conclusion Our data supported that miR-425 in BMSCs-Exos inhibits HILI by targeting PTEN and upregulating the PI3K/AKT axis. This study may provide personalized interventions for HILI remedy.
- Subjects :
- 0301 basic medicine
Cell
Biophysics
Lung injury
Exosomes
Biochemistry
Rats, Sprague-Dawley
03 medical and health sciences
Phosphatidylinositol 3-Kinases
stomatognathic system
medicine
PTEN
Animals
Viability assay
Molecular Biology
Protein kinase B
PI3K/AKT/mTOR pathway
Hyperoxia
030102 biochemistry & molecular biology
biology
business.industry
Mesenchymal stem cell
Mesenchymal Stem Cells
Lung Injury
Cell Hypoxia
Rats
Oxidative Stress
030104 developmental biology
medicine.anatomical_structure
biology.protein
Cancer research
medicine.symptom
business
Proto-Oncogene Proteins c-akt
Subjects
Details
- ISSN :
- 10960384
- Volume :
- 697
- Database :
- OpenAIRE
- Journal :
- Archives of biochemistry and biophysics
- Accession number :
- edsair.doi.dedup.....69250493410b26d01adeff6b0da86b2a