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Protease-activated receptor type 2 activation downregulates osteogenesis in periodontal ligament stem cells
FRANÇA, Bruno Nunes de; GASPARONI, Letícia Miquelitto; ROVAI, Emanuel Silva; AMBRÓSIO, Lucas Macedo Batitucci; MENDONÇA, Nathalia Felix de; HAGY, Marcos Hideki; MENDOZA, Aldrin HUAMÁN; SIPERT, Carla Renata; HOLZHAUSEN, Marinella.
Afiliación
  • FRANÇA, Bruno Nunes de; Universidade de São Paulo. School of Dentistry. Department of Stomatology. São Paulo. BR
  • GASPARONI, Letícia Miquelitto; Universidade de São Paulo. School of Dentistry. Department of Stomatology. São Paulo. BR
  • ROVAI, Emanuel Silva; Universidade de Taubaté. School of Dentistry. Periodontics Division. Taubaté. BR
  • AMBRÓSIO, Lucas Macedo Batitucci; Universidade de São Paulo. School of Dentistry. Department of Stomatology. São Paulo. BR
  • MENDONÇA, Nathalia Felix de; Universidade de São Paulo. School of Dentistry. Department of Stomatology. São Paulo. BR
  • HAGY, Marcos Hideki; Universidade de São Paulo. School of Dentistry. Department of Stomatology. São Paulo. BR
  • MENDOZA, Aldrin HUAMÁN; Universidade de São Paulo. School of Dentistry. Department of Stomatology. São Paulo. BR
  • SIPERT, Carla Renata; Universidade de São Paulo. School of Dentistry. Department of Restorative Dentistry. São Paulo. BR
  • HOLZHAUSEN, Marinella; Universidade de São Paulo. School of Dentistry. Department of Stomatology. São Paulo. BR
Braz. oral res. (Online) ; 37: e002, 2023. graf
Article en En | LILACS-Express | LILACS, BBO | ID: biblio-1420947
Biblioteca responsable: BR1.1
ABSTRACT
Abstract 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.
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Texto completo: 1 Índice: LILACS Idioma: En Revista: Braz. oral res. (Online) Asunto de la revista: ODONTOLOGIA Año: 2023 Tipo del documento: Article / Project document

Texto completo: 1 Índice: LILACS Idioma: En Revista: Braz. oral res. (Online) Asunto de la revista: ODONTOLOGIA Año: 2023 Tipo del documento: Article / Project document