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Liquid plasma promotes angiogenesis through upregulation of endothelial nitric oxide synthase-induced extracellular matrix metabolism: potential applications of liquid plasma for vascular injuries

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dc.contributor.authorKang, SU-
dc.contributor.authorKim, HJ-
dc.contributor.authorMa, S-
dc.contributor.authorOh, DY-
dc.contributor.authorJang, JY-
dc.contributor.authorSeo, C-
dc.contributor.authorLee, YS-
dc.contributor.authorKim, CH-
dc.date.accessioned2024-03-14T04:52:41Z-
dc.date.available2024-03-14T04:52:41Z-
dc.date.issued2024-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/32360-
dc.description.abstractBackground: Applications of nonthermal plasma have expanded beyond the biomedical field to include antibacterial, anti-inflammatory, wound healing, and tissue regeneration. Plasma enhances epithelial cell repair; however, the potential damage to deep tissues and vascular structures remains under investigation. Result: This study assessed whether liquid plasma (LP) increased nitric oxide (NO) production in human umbilical vein endothelial cells by modulating endothelial NO synthase (eNOS) phosphorylation and potential signaling pathways. First, we developed a liquid plasma product and confirmed the angiogenic effect of LP using the Matrigel plug assay. We found that the NO content increased in plasma-treated water. NO in plasma-treated water promoted cell migration and angiogenesis in scratch and tube formation assays via vascular endothelial growth factor mRNA expression. In addition to endothelial cell proliferation and migration, LP influenced extracellular matrix metabolism and matrix metalloproteinase activity. These effects were abolished by treatment with NG-L-monomethyl arginine, a specific inhibitor of NO synthase. Furthermore, we investigated the signaling pathways mediating the phosphorylation and activation of eNOS in LP-treated cells and the role of LKB1-adenosine monophosphate-activated protein kinase in signaling. Downregulation of adenosine monophosphate-activated protein kinase by siRNA partially inhibited LP-induced eNOS phosphorylation, angiogenesis, and migration. Conclusion: The present study suggests that LP treatment may be a novel strategy for promoting angiogenesis in vascular damage. A1BBJsagnHJAo-Bf8DXnP6 Video Abstract Graphical Abstract: (Figure presented.)-
dc.language.isoen-
dc.subject.MESHAdenosine Monophosphate-
dc.subject.MESHAngiogenesis-
dc.subject.MESHExtracellular Matrix-
dc.subject.MESHHuman Umbilical Vein Endothelial Cells-
dc.subject.MESHHumans-
dc.subject.MESHNeovascularization, Physiologic-
dc.subject.MESHNitric Oxide-
dc.subject.MESHNitric Oxide Synthase-
dc.subject.MESHNitric Oxide Synthase Type III-
dc.subject.MESHPhosphorylation-
dc.subject.MESHProtein Kinases-
dc.subject.MESHUp-Regulation-
dc.subject.MESHVascular Endothelial Growth Factor A-
dc.subject.MESHVascular System Injuries-
dc.titleLiquid plasma promotes angiogenesis through upregulation of endothelial nitric oxide synthase-induced extracellular matrix metabolism: potential applications of liquid plasma for vascular injuries-
dc.typeArticle-
dc.identifier.pmid38374138-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10875778-
dc.contributor.affiliatedAuthorKang, SU-
dc.contributor.affiliatedAuthorOh, DY-
dc.contributor.affiliatedAuthorJang, JY-
dc.contributor.affiliatedAuthorLee, YS-
dc.contributor.affiliatedAuthorKim, CH-
dc.type.localJournal Papers-
dc.identifier.doi10.1186/s12964-023-01412-w-
dc.citation.titleCell communication and signaling : CCS-
dc.citation.volume22-
dc.citation.number1-
dc.citation.date2024-
dc.citation.startPage138-
dc.citation.endPage138-
dc.identifier.bibliographicCitationCell communication and signaling : CCS, 22(1). : 138-138, 2024-
dc.identifier.eissn1478-811X-
dc.relation.journalidJ01478811X-
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Journal Papers > School of Medicine / Graduate School of Medicine > Otolaryngology
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