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Bioactive Nonthermal Biocompatible Plasma Enhances Migration on Human Gingival Fibroblasts

Ihn HanDepartment of Plasma Bio‐Display Kwangwoon University Seoul 01897 KoreaIn‐Seok SongDepartment of Dentistry Korea University Anam Hospital Seoul 02841 Republic of KoreaSeung Ah ChoiDivision of Pediatric Neurosurgery Pediatric Clinical Neuroscience Center Seoul National University Children's Hospital Seoul 03080 Republic of KoreaTae Bok LeeConfocal Core Facility Center for Medical Innovation Seoul National University Hospital Seoul 03082 KoreaMaksudbek YusupovResearch group PLASMANT Department of Chemistry University of Antwerp Universiteitsplein 1 Antwerp B‐2610 BelgiumPriyanka ShawResearch group PLASMANT Department of Chemistry University of Antwerp Universiteitsplein 1 Antwerp B‐2610 BelgiumAnnemie BogaertsResearch group PLASMANT Department of Chemistry University of Antwerp Universiteitsplein 1 Antwerp B‐2610 BelgiumEun Ha ChoiPlasma Bioscience Research Center Applied Plasma Medicine Center Kwangwoon University Seoul 01897 Republic of KoreaJae‐Jun RyuDepartment of Dentistry Korea University Anam Hospital Seoul 02841 Republic of Korea
2022en
ABI

Аннотация

This study hypothesizes that the application of low-dose nonthermal biocompatible dielectric barrier discharge plasma (DBD-NBP) to human gingival fibroblasts (HGFs) will inhibit colony formation but not cell death and induce matrix metalloproteinase (MMP) expression, extracellular matrix (ECM) degradation, and subsequent cell migration, which can result in enhanced wound healing. HGFs treated with plasma for 3 min migrate to each other across the gap faster than those in the control and 5-min treatment groups on days 1 and 3. The plasma-treated HGFs show significantly high expression levels of the cell cycle arrest-related p21 gene and enhanced MMP activity. Focal adhesion kinase (FAK) mediated attenuation of wound healing or actin cytoskeleton rearrangement, and plasma-mediated reversal of this attenuation support the migratory effect of DBD-NBP. Further, this work performs computer simulations to investigate the effect of oxidation on the stability and conformation of the catalytic kinase domain (KD) of FAK. It is found that the oxidation of highly reactive amino acids (AAs) Cys427, Met442, Cys559, Met571, Met617, and Met643 changes the conformation and increases the structural flexibility of the FAK protein and thus modulates its function and activity. Low-dose DBD-NBP-induces host cell cycle arrest, ECM breakdown, and subsequent migration, thus contributing to the enhanced wound healing process.

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