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https://hdl.handle.net/20.500.11851/8934
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DC Field | Value | Language |
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dc.contributor.author | Eren, Selen Kucukkaya | - |
dc.contributor.author | Zirh, Elham Bahador | - |
dc.contributor.author | Zirh, Selim | - |
dc.contributor.author | Sharafi, Parisa | - |
dc.contributor.author | Zeybek, Naciye Dilara | - |
dc.date.accessioned | 2022-11-30T19:23:57Z | - |
dc.date.available | 2022-11-30T19:23:57Z | - |
dc.date.issued | 2022 | - |
dc.identifier.issn | 1678-7757 | - |
dc.identifier.issn | 1678-7765 | - |
dc.identifier.uri | https://doi.org/10.1590/1678-7757-2022-0086 | - |
dc.identifier.uri | https://hdl.handle.net/20.500.11851/8934 | - |
dc.description.abstract | 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. | en_US |
dc.description.sponsorship | Hacettepe University Scientific Research Projects Coordination Unit [THD-2020-18625] | en_US |
dc.description.sponsorship | The 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). | en_US |
dc.language.iso | en | en_US |
dc.publisher | Univ Sao Paulo Fac Odontologia Bauru | en_US |
dc.relation.ispartof | Journal of Applied Oral Science | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Calcium silicate | en_US |
dc.subject | Cytotoxicity | en_US |
dc.subject | Osteogenic protein-1 | en_US |
dc.subject | Pulpotomy | en_US |
dc.subject | Regenerative endodontics | en_US |
dc.subject | Odontogenic Differentiation | en_US |
dc.subject | Irreversible Pulpitis | en_US |
dc.subject | Partial Pulpotomy | en_US |
dc.subject | Permanent Molars | en_US |
dc.subject | Teeth | en_US |
dc.subject | Tissue | en_US |
dc.subject | Sialoprotein | en_US |
dc.subject | Expression | en_US |
dc.subject | Immature | en_US |
dc.subject | Delivery | en_US |
dc.title | Combined Effects of Bone Morphogenetic Protein-7 and Mineral Trioxide Aggregate on the Proliferation, Migration, and Differentiation of Human Dental Pulp Stem Cells | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 30 | en_US |
dc.authorid | Bahador Zırh, Elham/0000-0002-6921-2365 | - |
dc.authorid | ZIRH, Selim/0000-0002-7962-6078 | - |
dc.identifier.wos | WOS:000855941800001 | en_US |
dc.identifier.scopus | 2-s2.0-85137775541 | en_US |
dc.institutionauthor | Bahador Zirh, Elham | - |
dc.institutionauthor | Sharafi, Parisa | - |
dc.identifier.pmid | 36102412 | en_US |
dc.identifier.doi | 10.1590/1678-7757-2022-0086 | - |
dc.authorwosid | Bahador Zırh, Elham/GWV-3753-2022 | - |
dc.authorwosid | ZIRH, Selim/AAP-4024-2020 | - |
dc.authorscopusid | 57191403740 | - |
dc.authorscopusid | 57221571018 | - |
dc.authorscopusid | 57207246752 | - |
dc.authorscopusid | 57193913814 | - |
dc.authorscopusid | 8540689700 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.scopusquality | Q1 | - |
dc.ozel | 2022v3_Edit | en_US |
item.openairetype | Article | - |
item.languageiso639-1 | en | - |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | 03.14. Department of Internal Medicine | - |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Temel Tıp Bilimleri Bölümü / Department of Basic Medical Sciences WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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