Combined effects of bone morphogenetic protein-7 and mineral trioxide aggregate on the proliferation, migration, and differentiation of human dental pulp stem cells

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Özet

Bioactive molecules present the potential to be used along with biomaterials in vital pulp therapy and regenerative endodontic treatment. Objective: The aim of this study was to assess the effects of the combined use of bone morphogenetic protein-7 (BMP-7) and mineral trioxide aggregate (MTA) on the proliferation, migration, and differentiation of human dental pulp stem cells (DPSCs). Methodology: For the proliferation analysis, DPSCs were incubated with a growth medium and treated with MTA and/or BMP-7 at different concentrations. For the following analyses, DPSCs were incubated with a differentiation medium and treated with MTA and/ or BMP-7. Moreover, there were groups in which DPSCs were incubated with the growth medium (control), the differentiation medium, or DMEM/F12 containing fetal bovine serum, and not treated with MTA or BMP-7. Cell proliferation was analyzed using the WST-1 assay. The odontogenic/osteogenic differentiation was evaluated by immunocytochemistry, alkaline phosphatase (ALP) activity assay, alizarin red staining, and reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Cell migration was evaluated using a wound-healing assay. Data were analyzed using analysis of variance and Tukey test (p=0.05). Results: The use of BMP-7 with MTA presented no significant effect on cell proliferation in comparison with the treatment with MTA alone (p>0.05), but showed higher ALP activity, increased mineralization, and higher expression of DMP1 and DSPP when compared with other groups (p<0.05). Nestin expression was higher in the control group than in groups treated with MTA and/or BMP-7 (p<0.05). The cell migration rate increased after treatment with MTA when compared with other groups in all periods of time (p<0.05). At 72 hours, the wound area was smaller in groups treated with MTA and/ or BMP-7 than in the control group (p<0.05). Conclusion: The use of BMP-7 with MTA increased odontogenic/osteogenic differentiation without adversely affecting proliferation and migration of DPSCs. The use of BMP-7 with MTA may improve treatment outcomes by increasing repair and regeneration capacity of DPSCs. © 2022, Faculdade de Odontologia de Bauru da Universidade de Sao Paulo. All rights reserved.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/12973Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1590/1678-7757-2022-0086Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorKüçükkaya Eren, Selen
dc.contributor.authorBahador Zirh, Elham
dc.contributor.authorZirh, Selim
dc.contributor.authorSharafi, Parisa
dc.contributor.authorZeybek, Naciye Dilara
dc.date.accessioned2026-10-18T20:27:49.798917266Z
dc.date.available2026-10-18T20:27:49.798917266Z
dc.date.issued2022
dc.description.abstractBioactive molecules present the potential to be used along with biomaterials in vital pulp therapy and regenerative endodontic treatment. Objective: The aim of this study was to assess the effects of the combined use of bone morphogenetic protein-7 (BMP-7) and mineral trioxide aggregate (MTA) on the proliferation, migration, and differentiation of human dental pulp stem cells (DPSCs). Methodology: For the proliferation analysis, DPSCs were incubated with a growth medium and treated with MTA and/or BMP-7 at different concentrations. For the following analyses, DPSCs were incubated with a differentiation medium and treated with MTA and/ or BMP-7. Moreover, there were groups in which DPSCs were incubated with the growth medium (control), the differentiation medium, or DMEM/F12 containing fetal bovine serum, and not treated with MTA or BMP-7. Cell proliferation was analyzed using the WST-1 assay. The odontogenic/osteogenic differentiation was evaluated by immunocytochemistry, alkaline phosphatase (ALP) activity assay, alizarin red staining, and reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Cell migration was evaluated using a wound-healing assay. Data were analyzed using analysis of variance and Tukey test (p=0.05). Results: The use of BMP-7 with MTA presented no significant effect on cell proliferation in comparison with the treatment with MTA alone (p>0.05), but showed higher ALP activity, increased mineralization, and higher expression of DMP1 and DSPP when compared with other groups (p<0.05). Nestin expression was higher in the control group than in groups treated with MTA and/or BMP-7 (p<0.05). The cell migration rate increased after treatment with MTA when compared with other groups in all periods of time (p<0.05). At 72 hours, the wound area was smaller in groups treated with MTA and/ or BMP-7 than in the control group (p<0.05). Conclusion: The use of BMP-7 with MTA increased odontogenic/osteogenic differentiation without adversely affecting proliferation and migration of DPSCs. The use of BMP-7 with MTA may improve treatment outcomes by increasing repair and regeneration capacity of DPSCs. © 2022, Faculdade de Odontologia de Bauru da Universidade de Sao Paulo. All rights reserved.
dc.description.sponsorshipThe authors declare no conflict of interest related to this study. This study was supported by the Hacettepe University Scientific Research Projects Coordination Unit (THD-2020-18625).
dc.identifier.doi10.1590/1678-7757-2022-0086
dc.identifier.eissn1678-7765
dc.identifier.issn1678-7757
dc.identifier.pmcidPMC9469872
dc.identifier.pmid36102412
dc.identifier.scopus2-s2.0-85137775541
dc.identifier.startpagee20220086
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12973
dc.identifier.volume30
dc.identifier.wosWOS:000855941800001
dc.language.isoen
dc.publisherFaculdade de Odontologia de Bauru da Universidade de Sao Paulo
dc.relation.ispartofJournal of Applied Oral Science
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCalcium silicate
dc.subjectCytotoxicity
dc.subjectOsteogenic protein-1
dc.subjectPulpotomy
dc.subjectRegenerative endodontics
dc.subjectAluminum Compounds
dc.subjectBone Morphogenetic Protein 7
dc.subjectCalcium Compounds
dc.subjectCell Proliferation
dc.subjectDental Pulp
dc.subjectDrug Combinations
dc.subjectHumans
dc.subjectOsteogenesis
dc.subjectOxides
dc.subjectPemetrexed
dc.subjectSilicates
dc.subjectStem Cells
dc.subjectaluminum derivative
dc.subjectcalcium derivative
dc.subjectmineral trioxide aggregate
dc.subjectosteogenic protein 1
dc.subjectoxide
dc.subjectsilicate
dc.subjectbone development
dc.subjectdrug combination
dc.subjecthuman
dc.subjectstem cell
dc.subjecttooth pulp
dc.titleCombined effects of bone morphogenetic protein-7 and mineral trioxide aggregate on the proliferation, migration, and differentiation of human dental pulp stem cells
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus9
rdl.citation.wos9
rdl.departmentErzincan Binali Yıldırım University, Faculty of Medicine, Department of Histology and Embryology, Erzincan, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)