Boron Regulates Mineralized Tissue-Associated Proteins in Osteoblasts (MC3T3-E1)

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dc.contributor.authorHakkı, Sema S.
dc.contributor.authorBozkurt, Buket S.
dc.contributor.authorHakkı, Erdoğan E.
dc.date.accessioned2020-03-26T17:47:17Z
dc.date.available2020-03-26T17:47:17Z
dc.date.issued2010
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractThe aim of this study was to determine the effects of boron (B) on the cell-survival, proliferation, mineralization and mRNA expression of mineralized tissue-associated proteins. Additionally, determination of the effects of B on the BMP-4, -6 and -7 protein levels of pre-osteoblastic cells (MC3T3-E1) was also intended. The effects of B (pH 7.0) concentrations (0, 0.1, 1, 10, 100, 1000, 2000, 4000, 8000 and 10,000 ng/ml) on the survival of the cells were evaluated at 24 and 96 hrs with MTT assay. To evaluate the proliferation in long term, MC3T3-E1 cells were treated with different concentrations of B (0, 0.1, 1, 10, 100 and 1000 ng/ml) and were counted on days 2, 5, and 14. While in short term, decreased cell survival rate was observed at 1000 ng/ml and above, at long term no statistically significant difference was detected in different B concentrations applied. Slight decreases at the proliferation of the B-treated groups were determined on days 5 and 14 but one-way analysis of variance revealed that the difference was statistically insignificant. In mineralization assay, increased mineralized nodules were apparently observed in B treatment (1 and 10 ng/ml concentrations) groups. Based on quantitative RT-PCR results, remarkable regulation in favor of osteoblastic function for Collagen type I (COL I), Osteopontin (OPN), Bone Sialoprotein (BSP), Osteocalcin (OCN) and RunX2 mRNA expressions were observed in B treatment groups in comparison with untreated control groups. Increased BMP-4, -6 and -7 protein levels were detected at 0.1, 1, 10 and 100 ng/ml B concentrations. Results of the study suggest that at the molecular level B displays important roles on bone metabolism and may find novel usages at the regenerative medicine.en_US
dc.description.sponsorshipNational Boron Research Institute [TURKIYE/BOREN-2006-08-C07-10]en_US
dc.description.sponsorshipThis study was performed in Research Center of Dental Faculty, Selcuk University. This project was supported by The National Boron Research Institute-TURKIYE/BOREN-2006-08-C07-10. The authors are grateful to Engin U. Akkaya for critical comments on the manuscript and to Niyazi Dundar for technical assistance performing ELISA.en_US
dc.identifier.citationHakkı, S. S., Bozkurt, B. S., Hakkı, E. E., (2010). Boron Regulates Mineralized Tissue-Associated Proteins in Osteoblasts (MC3T3-E1). Journal of Trace Elements in Medicine and Biology, 24(4), 243-250. Doi: 10.1016/j.jtemb.2010.03.003
dc.identifier.doi10.1016/j.jtemb.2010.03.003en_US
dc.identifier.endpage250en_US
dc.identifier.issn0946-672Xen_US
dc.identifier.issue4en_US
dc.identifier.pmid20685097en_US
dc.identifier.scopusqualityQ1en_US
dc.identifier.startpage243en_US
dc.identifier.urihttps://dx.doi.org/10.1016/j.jtemb.2010.03.003
dc.identifier.urihttps://hdl.handle.net/20.500.12395/24665
dc.identifier.volume24en_US
dc.identifier.wosWOS:000286018200004en_US
dc.identifier.wosqualityQ3en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.institutionauthorHakkı, Sema S.
dc.institutionauthorBozkurt, Buket S.
dc.institutionauthorHakkı, Erdoğan E.
dc.language.isoenen_US
dc.publisherElsevier Gmbh, Urban & Fischer Verlagen_US
dc.relation.ispartofJournal of Trace Elements in Medicine and Biologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectBoronen_US
dc.subjectOsteoblastsen_US
dc.subjectMineralized tissueen_US
dc.subjectBoneen_US
dc.subjectBmpsen_US
dc.titleBoron Regulates Mineralized Tissue-Associated Proteins in Osteoblasts (MC3T3-E1)en_US
dc.typeArticleen_US

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