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Cell sheet produced from periodontal ligament stem cells activated by PAR1 improves osteogenic differentiation

dc.contributor.authorGasparoni, Letícia Miquelitto
dc.contributor.authorAlves, Tomaz
dc.contributor.authorFrança, Bruno Nunes de
dc.contributor.authorBalzarini, Danilo
dc.contributor.authorAlbuquerque-Souza, Emmanuel
dc.contributor.authorPedroni, Ana Clara Fagundes
dc.contributor.authorRovai, Emanuel da Silva [UNESP]
dc.contributor.authorMendoza, Aldrin Huamán
dc.contributor.authorSipert, Carla Renata
dc.contributor.authorHolzhausen, Marinella
dc.contributor.institutionSchool of Dentistry
dc.contributor.institutionDivision of Comprehensive Oral Health
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionWilliam Harvey Research Institute
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T20:02:35Z
dc.date.issued2024-01-01
dc.description.abstractPeriodontal regeneration is a challenge, and tissue engineering based on periodontal ligament stem cells (PDLSCs) has been shown to be a promising alternative to this process. However, the need for scaffolds has limited the therapeutic use of PDLSCs. In this context, scaffold-free tissue engineering using the cell sheet (CS) technique has been developed as an alternative approach to improve tissue regeneration. Previously, we showed that Protease-activated receptor-1 (PAR1) can regulate PDLSCs. Herein, we evaluate whether PAR1 influences osteogenesis in CSs produced from PDLSCs, without the use of scaffolds. PDLSCs were isolated and immunophenotyped. Then, CSs were obtained by supplementing the culture medium with ascorbic acid (50 µg/mL), and PAR1 was activated through its agonist peptide (100 nM). Scaffold-free 3D CSs were successfully produced from PDLSCs, and they showed higher proliferation potential than isolated PDLSCs. Also, PAR1 activation decreased senescence and improved osteogenic differentiation of CSs by increasing mineralized nodule deposition and alkaline phosphatase concentration; PAR1 also modulated osteogenic markers at the gene and protein levels. We further demonstrated that this effect was regulated by Wnt, TGF-βI, MEK, p38 MAPK, and FGF/VEGF signaling pathways in PDLSCs (p < 0.05%). Overall, PAR1 activation increased osteogenic activity in CSs, emerging as a promising scaffold-free therapeutic approach for periodontal regeneration.en
dc.description.affiliationUniversidade Federal de Juiz de Fora UFJF School of Dentistry Department of Dental Clinic, MG
dc.description.affiliationUniversity of North Carolina Adams School of Dentistry Division of Comprehensive Oral Health
dc.description.affiliationUniversidade São Francisco – USF School of Dentistry, Bragança Paulista, SP
dc.description.affiliationUniversidade de São Paulo – USP School of Dentistry Department of Stomatology, SP
dc.description.affiliationQueen Mary University William Harvey Research Institute
dc.description.affiliationUniversidade de São Paulo – USP School of Dentistry Department of Restorative Dentistry, SP
dc.description.affiliationUniversidade Estadual Paulista – Unesp Institute of Science and Technology Division of Periodontics, SP
dc.description.affiliationUnespUniversidade Estadual Paulista – Unesp Institute of Science and Technology Division of Periodontics, SP
dc.identifierhttp://dx.doi.org/10.1590/1807-3107bor-2024.vol38.0079
dc.identifier.citationBrazilian Oral Research, v. 38.
dc.identifier.doi10.1590/1807-3107bor-2024.vol38.0079
dc.identifier.issn1807-3107
dc.identifier.issn1806-8324
dc.identifier.scopus2-s2.0-85204084491
dc.identifier.urihttps://hdl.handle.net/11449/305248
dc.language.isoeng
dc.relation.ispartofBrazilian Oral Research
dc.sourceScopus
dc.subjectCell Culture Techniques
dc.subjectOsteogenesis
dc.subjectPeriodontal Ligament
dc.subjectProtease-Activated
dc.subjectReceptors
dc.subjectStem Cells
dc.titleCell sheet produced from periodontal ligament stem cells activated by PAR1 improves osteogenic differentiationen
dc.typeArtigopt
dspace.entity.typePublication

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