Journal
JOURNAL OF BIOMATERIALS AND TISSUE ENGINEERING
Volume 12, Issue 1, Pages 206-214Publisher
AMER SCIENTIFIC PUBLISHERS
DOI: 10.1166/jbt.2022.2658
Keywords
Deep VenousThrombosis; Endothelial Prgenitor Cells; miRNA-130a; MMP-1; Angiogenesis
Categories
Funding
- National Natural Science Foundation of China [81770483, 81800418]
- Natural Science Foun-dation of Jiangsu Province [BK20180125]
- Medical Science and technology development Foundation [YKK18063]
Ask authors/readers for more resources
This study investigated the effects and mechanisms of miRNA-130a in human endothelial progenitor cells (EPCs) involved in deep vein thrombosis (DVT). The results showed that miRNA-130a promotes migration, invasion, and tube formation of EPCs by positively regulating the expression of MMP-1 through Akt/PI3K/mTOR signaling pathway.
Aim: In this study, we aimed to investigate the effects and mechanisms of miRNA-130a in human endothelial progenitor cells (EPCs) involved in Deep vein thrombosis (DVT). Methods: EPCs were isolated and identified by cell morphology and surface marker detection. The effect of miR-130a on the migration, invasion and angiogenesis of EPCs in vitro were also detected. In addition, whether miR-130a is involved in the MMP-1 expression and Akt/PI3K/mTOR signaling pathway was also demonstrated. Results: Results suggested that miRNA-130a promotes migration, invasion, and tube formation of EPCs by positively regulating the expression of MMP-1 through Akt/PI3K/mTOR signaling pathway. Conclusion: Thus, as a potential therapeutic target, miRNA-130a may play an important role in the treatment of DVT.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available