Laser Photobiomodulation 808nm: Effects on Gene Expression in Inflammatory and Osteogenic Biomarkers in Human Dental Pulp Stem Cells

被引:5
|
作者
da Rocha, Elaine A. [1 ]
Alvarez, Marcela M. P. [2 ]
Pelosine, Agatha M. [3 ]
Carrilho, Marcela Rocha O. [4 ]
Tersariol, Ivarne L. S. [2 ]
Nascimento, Fabio D. [1 ,2 ,3 ]
机构
[1] Mogi das Cruzes Univ, Technol Res Ctr, Mogi Das Cruzes, SP, Brazil
[2] Univ Fed Sao Paulo, Dept Biochem, Sao Paulo, Brazil
[3] Univ Mogi das Cruzes, Interdisciplinary Ctr Biochem Invest, Mogi Das Cruzes, SP, Brazil
[4] Midwestern Univ, Coll Dent Med Illinois, Downers Grove, IL 60515 USA
基金
巴西圣保罗研究基金会;
关键词
human dental pulp stem cells; photobiomodualtion therapy; gene expreesion; dental pulp stem cells; inflammation; bone osteogenesis; ENGINEERED HYBRID TOOTH; NF-KAPPA-B; TRANSCRIPTION FACTOR; MOLECULAR-CLONING; IN-VITRO; THERAPY; DIFFERENTIATION; PROLIFERATION; IRRADIATION; LIGHT;
D O I
10.3389/fphar.2021.782095
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The tissue engineering of dental oral tissue is tackling significant advances and the use of stem cells promises to boost the therapeutical approaches of regenerative dentistry. Despite advances in this field, the literature is still scarce regarding the modulatory effect of laser photobiomodulation (PBM) on genes related to inflammation and osteogenesis in Postnatal Human Dental Pulp Stem cells (DPSCs). This study pointedly investigated the effect of PBM treatment in proliferation, growth and differentiation factors, mineralization, and extracellular matrix remodeling genes in DPSCs. Freshly extracted human third molars were used as a source for DPSCs isolation. The isolated DPSCs were stimulated to an inflammatory state, using a lipopolysaccharide (LPS) model, and then subjected or not to laser PBM. Each experiment was statistically evaluated according to the sample distribution. A total of 85 genes related to inflammation and osteogenesis were evaluated regarding their expression by RT-PCR. Laser PBM therapy has shown to modulate several genes expression in DPSCs. PBM suppressed the expression of inflammatory gene TNF and RANKL and downregulated the gene expression for VDR and proteolytic enzymes cathepsin K, MMP-8 and MMP-9. Modulation of gene expression for proteinase-activated receptors (PARs) following PBM varied among different PARs. As expected, PBM blocked the odontoblastic differentiation of DPSCs when subjected to LPS model. Conversely, PBM has preserved the odontogenic potential of DPSCs by increasing the expression of TWIST-1/RUNEX-2/ALP signaling axis. PBM therapy notably played a role in the DPSCs genes expression that mediate inflammation process and tissue mineralization. The present data opens a new perspective for PBM therapy in mineralized dental tissue physiology.
引用
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页数:9
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