Shoma Yamamori , Eri Urano-Morisawa , Ayako Mochizuki , Ryo Aizawa , Fuminori Iwasa , Matsuo Yamamoto , Kazuyoshi Baba
{"title":"Mirror-polished ceria-stabilized zirconia/alumina nanocomposite enhances gingival junctional epithelial cell adhesion","authors":"Shoma Yamamori , Eri Urano-Morisawa , Ayako Mochizuki , Ryo Aizawa , Fuminori Iwasa , Matsuo Yamamoto , Kazuyoshi Baba","doi":"10.1016/j.job.2024.100593","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><div>The aim of this study was to determine the optimal surface roughness (Ra) of ceria-stabilized zirconia/alumina nanocomposite (Ce-TZP/Al₂O₃) implants for mouse gingival junctional epithelial cell (JE-1) adhesion and soft tissue sealing <em>in vitro</em>.</div></div><div><h3>Methods</h3><div>Titanium and Ce-TZP/Al₂O₃ disks were prepared, mechanically polished (M), and mirror-polished (Mr). The surface morphology of each disk was evaluated, and the Ra was measured using scanning electron microscopy and atomic force microscopy. JE-1 cells were cultured on each disk, and cell proliferation was assessed by measuring the absorbance using the MTS assay. We also analyzed the expression of the adhesion proteins Laminin-5, Integrin β4, and Cadherin-1 using immunostaining and quantitative reverse transcription-polymerase chain reaction (qRT-PCR). The adhesion strength of the JE-1 cells to each disk was measured using a shaking stimulation test.</div></div><div><h3>Results</h3><div>M disks had rough surfaces, whereas Mr disks had smooth morphologies. JE-1 cell proliferation was proportional to the culture time, and the Mr disks showed higher values than the M disk. Immunofluorescence and qRT-PCR showed that expression of Laminin-5 and Integrin β4 was higher with Mr disks than with M on the Ce-TZP/Al₂O₃ disks. The oscillatory stimulation test also showed that the adhesive strength of JE-1 cells was significantly higher with Mr than with M on the Ce-TZP/Al₂O₃ disks.</div></div><div><h3>Conclusions</h3><div>Mirror polishing of Ce-TZP/Al₂O₃ disks enhances epithelial cell proliferation and adhesion more than mechanical polishing. These findings have implications for the optimization of implant surface characteristics to improve epithelial sealing.</div></div>","PeriodicalId":45851,"journal":{"name":"Journal of Oral Biosciences","volume":"67 1","pages":"Article 100593"},"PeriodicalIF":2.6000,"publicationDate":"2024-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Oral Biosciences","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1349007924002421","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives
The aim of this study was to determine the optimal surface roughness (Ra) of ceria-stabilized zirconia/alumina nanocomposite (Ce-TZP/Al₂O₃) implants for mouse gingival junctional epithelial cell (JE-1) adhesion and soft tissue sealing in vitro.
Methods
Titanium and Ce-TZP/Al₂O₃ disks were prepared, mechanically polished (M), and mirror-polished (Mr). The surface morphology of each disk was evaluated, and the Ra was measured using scanning electron microscopy and atomic force microscopy. JE-1 cells were cultured on each disk, and cell proliferation was assessed by measuring the absorbance using the MTS assay. We also analyzed the expression of the adhesion proteins Laminin-5, Integrin β4, and Cadherin-1 using immunostaining and quantitative reverse transcription-polymerase chain reaction (qRT-PCR). The adhesion strength of the JE-1 cells to each disk was measured using a shaking stimulation test.
Results
M disks had rough surfaces, whereas Mr disks had smooth morphologies. JE-1 cell proliferation was proportional to the culture time, and the Mr disks showed higher values than the M disk. Immunofluorescence and qRT-PCR showed that expression of Laminin-5 and Integrin β4 was higher with Mr disks than with M on the Ce-TZP/Al₂O₃ disks. The oscillatory stimulation test also showed that the adhesive strength of JE-1 cells was significantly higher with Mr than with M on the Ce-TZP/Al₂O₃ disks.
Conclusions
Mirror polishing of Ce-TZP/Al₂O₃ disks enhances epithelial cell proliferation and adhesion more than mechanical polishing. These findings have implications for the optimization of implant surface characteristics to improve epithelial sealing.