The Response of Cementoblasts To Calcium Phosphate Resin-Based and Calcium Silicate-Based Commercial Sealers

dc.contributor.author Hakki, S. S.
dc.contributor.author Bozkurt, B. S.
dc.contributor.author Ozcopur, B.
dc.contributor.author Gandolfi, M. G.
dc.contributor.author Prati, C.
dc.contributor.author Belli, S.
dc.date.accessioned 2025-05-10T17:44:41Z
dc.date.available 2025-05-10T17:44:41Z
dc.date.issued 2013
dc.description Prati, Carlo/0000-0001-8163-8628; Belli, Sema/0000-0002-7240-7649; Gandolfi, Maria Giovanna/0000-0001-7793-6227; Hakki, Sema/0000-0001-8665-6235 en_US
dc.description.abstract Hakki SS, Bozkurt BS, Ozcopur B, Gandolfi MG, Prati C, Belli S. The response of cementoblasts to calcium phosphate resin-based and calcium silicate-based commercial sealers. International Endodontic Journal, 46, 242-252, 2013. Aim To investigate cell viability and gene expression of cementoblasts (OCCM.30) exposed to extractable components released by resin-based sealers with different chemical composition Hybrid Root Seal (HRS), SimpliSeal (SS), Real Seal (RS) and AH Plus (AH) and by a MTA-based sealers Tech Biosealer Endo (TBE). Methodology Discs of all materials were prepared and allowed to set in humid conditions at 37 degrees for 48h. The discs were then incubated for 72h at 37 degrees C to obtain material extracts (1/1) in DMEM. The extracts containing the components released by the sealers were filtered and other dilutions (1/2, 1/4) were prepared from the original solution (1/1). Original and diluted solutions were tested on the cementoblasts. Impedance-based real-time cell analysis (RTCA) was used to evaluate cell viability, quantitative real-time polymerase chain reaction (QRT-PCR) was used to examine the expression of mineralization-related genes (osteocalcin; OCN, Runt-related transcription factor-2; Runx2, collagen type 1; COL I, alkaline phosphatase; ALP). For statistical analysis, one-way analysis of variance (anova) and Tukey's honestly significant difference (HSD) tests were used. Results TBE (1/2), RS (1/2, 1/4), and HRS (1/2, 1/4) significantly decreased cell viability (P<0.001). AH (1/2, 1/4) and SS (1/2, 1/4) had similar cell viability to the control at 30h. All tested materials significantly decreased cell viability when compared to the control group except AH (1/2, 1/4) and SS (1/4) at 90h. All of the tested sealers reduced COL I mRNA expressions when compared to the control. SS was associated with significant increases in OCN and Runx2 mRNA expressions when compared to the control (P<0.001). Whereas all of the dilutions of TBE, RS and HRS significantly decreased BSP mRNA expressions (P<0,001), 1/2 and 1/4 dilutions of SS increased BSP mRNA expression (P<0,001). Except the 1/4 dilutions of AH and SS, all the sealer dilutions significantly reduced ALP mRNA expression in cementoblasts (P<0,001). Conclusions SimpliSeal and AH Plus resulted in more favourable response to cementoblasts because of their regulation potential on the mineralized tissue-associated protein's mRNA expressions. en_US
dc.description.sponsorship Research Projects Center of Selcuk University (BAP) Konya, Turkey en_US
dc.description.sponsorship The authors deny any conflicts of interest. This study was supported in part by Research Projects Center of Selcuk University (BAP) Konya, Turkey. The materials are generously supplied by the companies. en_US
dc.identifier.doi 10.1111/j.1365-2591.2012.02122.x
dc.identifier.issn 0143-2885
dc.identifier.issn 1365-2591
dc.identifier.scopus 2-s2.0-84873567535
dc.identifier.uri https://doi.org/10.1111/j.1365-2591.2012.02122.x
dc.identifier.uri https://hdl.handle.net/20.500.14720/16122
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Calcium Fluoro Silicate Cement en_US
dc.subject Cell Proliferation en_US
dc.subject Cell Viability en_US
dc.subject Cytotoxicity en_US
dc.subject Endodontics en_US
dc.subject Mrna en_US
dc.title The Response of Cementoblasts To Calcium Phosphate Resin-Based and Calcium Silicate-Based Commercial Sealers en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Prati, Carlo/0000-0001-8163-8628
gdc.author.id Belli, Sema/0000-0002-7240-7649
gdc.author.id Gandolfi, Maria Giovanna/0000-0001-7793-6227
gdc.author.id Hakki, Sema/0000-0001-8665-6235
gdc.author.scopusid 6603544775
gdc.author.scopusid 36443208800
gdc.author.scopusid 35320261700
gdc.author.scopusid 7005240959
gdc.author.scopusid 7006322243
gdc.author.scopusid 7007091407
gdc.author.wosid Hakkı, Sema/Y-2878-2018
gdc.author.wosid Bozkurt, Serife/M-5852-2017
gdc.author.wosid Belli, Sema/Glr-5467-2022
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Hakki, S. S.; Bozkurt, B. S.] Selcuk Univ, Dept Periodontol, Konya, Turkey; [Ozcopur, B.] Yuzuncu Yil Univ, Fac Dent, Dept Operat Dent, Van, Turkey; [Gandolfi, M. G.; Prati, C.] Univ Bologna, Dept Odontostomatol Sci, Lab Biomat, Bologna, Italy; [Belli, S.] Selcuk Univ, Dept Endodont, Konya, Turkey en_US
gdc.description.endpage 252 en_US
gdc.description.issue 3 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.startpage 242 en_US
gdc.description.volume 46 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q1
gdc.identifier.pmid 23005923
gdc.identifier.wos WOS:000314922000008
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

Files