Effect of Hyperbaric Oxygen and Inflammation on Human Gingival Mesenchymal Stem/Progenitor Cells

被引:4
作者
Toelle, Johannes [1 ]
Koch, Andreas [2 ]
Schlicht, Kristina [3 ]
Finger, Dirk [1 ]
Kaehler, Wataru [2 ]
Hoeppner, Marc [4 ]
Graetz, Christian [1 ]
Doerfer, Christof [1 ]
Schulte, Dominik M. [3 ,5 ]
Fawzy El-Sayed, Karim [1 ,6 ]
机构
[1] Univ Kiel, Sch Dent Med, Clin Conservat Dent & Periodontol, D-24105 Kiel, Germany
[2] German Naval Med Inst, D-24119 Kiel, Germany
[3] Univ Hosp Schleswig Holstein, Inst Diabet & Clin Metab Res, D-24105 Kiel, Germany
[4] Univ Kiel, Inst Clin Mol Biol, Sch Med, D-24105 Kiel, Germany
[5] Univ Hosp Schleswig Holstein, Dept Internal Med 1, Div Endocrinol Diabet & Clin Nutr, D-24105 Kiel, Germany
[6] Cairo Univ, Fac Dent, Oral Med & Periodontol Dept, Cairo 12613, Egypt
关键词
inflammation; stem cells; hyperbaric oxygen; regeneration; periodontitis; ROS; next-generation sequencing; OSTEOGENIC DIFFERENTIATION; EXPRESSION PROFILE; OXIDATIVE STRESS; STROMAL CELLS; BONE-MARROW; STEM-CELLS; TNF-ALPHA; THERAPY; PERIODONTITIS; IL-1-BETA;
D O I
10.3390/cells12202479
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The present study explores for the first time the effect of hyperbaric oxygen (HBO) on gingival mesenchymal stem cells' (G-MSCs) gene expression profile, intracellular pathway activation, pluripotency, and differentiation potential under an experimental inflammatory setup. G-MSCs were isolated from five healthy individuals (n = 5) and characterized. Single (24 h) or double (72 h) HBO stimulation (100% O2, 3 bar, 90 min) was performed under experimental inflammatory [IL-1 beta (1 ng/mL)/TNF-alpha (10 ng/mL)/IFN-gamma (100 ng/mL)] and non-inflammatory micro-environment. Next Generation Sequencing and KEGG pathway enrichment analysis, G-MSCs' pluripotency gene expression, Wnt-/beta-catenin pathway activation, proliferation, colony formation, and differentiation were investigated. G-MSCs demonstrated all mesenchymal stem/progenitor cells' characteristics. The beneficial effect of a single HBO stimulation was evident, with anti-inflammatory effects and induction of differentiation (TLL1, ID3, BHLHE40), proliferation/cell survival (BMF, ID3, TXNIP, PDK4, ABL2), migration (ABL2) and osteogenic differentiation (p < 0.05). A second HBO stimulation at 72 h had a detrimental effect, significantly increasing the inflammation-induced cellular stress and ROS accumulation through HMOX1, BHLHE40, and ARL4C amplification and pathway enrichment (p < 0.05). Results outline a positive short-term single HBO anti-inflammatory, regenerative, and differentiation stimulatory effect on G-MSCs. A second (72 h) stimulation is detrimental to the same properties. The current results could open new perspectives in the clinical application of short-termed HBO induction in G-MSCs-mediated periodontal reparative/regenerative mechanisms.
引用
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页数:16
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