Protease-activated receptor type 2 activation downregulates osteogenesis in periodontal ligament stem cells.
Bruno Nunes de FrançaLetícia Miquelitto GasparoniEmanuel da Silva RovaiLucas Macedo Batitucci AmbrósioNathalia Felix de MendonçaMarcos Hideki HagyAldrin Huamán MendozaCarla Renata SipertMarinella HolzhausenPublished in: Brazilian oral research (2023)
Protease-activated receptor-2 (PAR2) is associated with the pathogenesis of many chronic diseases with inflammatory characteristics, including periodontitis. This study aimed to evaluate how the activation of PAR2 can affect the osteogenic activity of human periodontal ligament stem cells (PDLSCs) in vitro. PDLSCs collected from three subjects were treated in osteogenic medium for 2, 7, 14, and 21 days with trypsin (0.1 U/mL), PAR2 specific agonist peptide (SLIGRL-NH2) (100 nM), and PAR2 antagonist peptide (FSLLRY-NH2) (100 nM). Gene (RT-qPCR) expression and protein expression (ELISA) of osteogenic factors, bone metabolism, and inflammatory cytokines, cell proliferation, alkaline phosphatase (ALP) activity, alizarin red S staining, and supernatant concentration were assessed. Statistical analysis of the results with a significance level of 5% was performed. Activation of PAR2 led to decreases in cell proliferation and calcium deposition (p < 0.05), calcium concentration (p < 0.05), and ALP activity (p < 0.05). Additionally, PAR2 activation increased gene and protein expression of receptor activator of nuclear factor kappa-Β ligand (RANKL) (p < 0.05) and significantly decreased the gene and protein expression of osteoprotegerin (p <0. 05). Considering the findings, the present study demonstrated PAR2 activation was able to decrease cell proliferation, decreased osteogenic activity of PDLSCs, and upregulated conditions for bone resorption. PAR2 may be considered a promising target in periodontal regenerative procedures.
Keyphrases
- nuclear factor
- stem cells
- cell proliferation
- mesenchymal stem cells
- toll like receptor
- bone marrow
- cell cycle
- copy number
- genome wide
- cell therapy
- bone mineral density
- photodynamic therapy
- immune response
- room temperature
- dna methylation
- oxidative stress
- postmenopausal women
- long non coding rna
- signaling pathway
- ionic liquid
- induced pluripotent stem cells
- genome wide analysis