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dc.contributor.authorCalciolari, Een_US
dc.contributor.authorMardas, Nen_US
dc.contributor.authorDereka, Xen_US
dc.contributor.authorAnagnostopoulos, AKen_US
dc.contributor.authorTsangaris, GTen_US
dc.contributor.authorDonos, Nen_US
dc.date.accessioned2017-11-03T11:07:29Z
dc.date.available2017-08-13en_US
dc.date.issued2018-04en_US
dc.date.submitted2017-10-25T10:30:07.687Z
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/28598
dc.description.abstractBACKGROUND AND OBJECTIVES: There is significant evidence that, during the early stages of osseointegration, moderately rough hydrophilic (SLActive) surfaces can accelerate osteogenesis and increase bone-to-implant contact in comparison to hydrophobic (SLA) surfaces. However, very little is known regarding the molecular mechanisms behind the influence that surface chemistry modifications to increase hydrophilicity determine on bone healing. The aim of this study was to describe for the first time the proteins and related signalling pathways expressed during early osseous healing stages under SLA and SLActive titanium domes for guided bone regeneration. MATERIAL AND METHODS: One SLA and 1 SLActive dome with an internal diameter of 5.0 mm and a height of 3.0 mm were secured to the parietal bones of nine 6-month-old male New Zealand rabbits. Three animals were randomly euthanized at 4, 7 and 14 days and the newly formed tissues retrieved under the domes were analysed with liquid chromatography-mass spectrometry/mass spectrometry. STRING and KEGG databases were applied for Gene Ontology and pathway analyses. RESULTS: A different modulation of several pathways was detected between the 2 groups at all healing times. The main differences in the osseous healing response associated to the 2 surfaces were related to pathways involved in regulating the inflammatory response, differentiation of osteoblast precursors and skeletogenesis. At day 7, the highest number of proteins and the highest cellular activity were observed in both groups, although a more complex and articulated proteome in terms of cellular metabolism and signal transduction was observed in SLActive samples. CONCLUSION: This is the first study describing the proteome expressed during early healing stages of guided bone regeneration and osseointegration. A combination of enhanced early osteogenic response and reduced inflammatory response were suggested for the hydrophilic group. Future studies are needed to corroborate these findings and explore the molecular effects of different titanium surfaces on the cascade of events taking place during bone formation.en_US
dc.format.extent174 - 187en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofJ Periodontal Resen_US
dc.rightsThis is the peer reviewed version of the following article: Calciolari E, Mardas N, Dereka X, Anagnostopoulos AK, Tsangaris GT, Donos N. Protein expression during early stages of bone regeneration under hydrophobic and hydrophilic titanium domes. A pilot study. J Periodont Res. 2017;00:1–14., which has been published in final form at https://doi.org/10.1111/jre.12498. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
dc.subjectguided bone regenerationen_US
dc.subjectosseointegrationen_US
dc.subjectsurface chemistryen_US
dc.subjectwound healingen_US
dc.subjectAnimalsen_US
dc.subjectCell Differentiationen_US
dc.subjectDental Implantsen_US
dc.subjectHydrophobic and Hydrophilic Interactionsen_US
dc.subjectMaleen_US
dc.subjectOsseointegrationen_US
dc.subjectOsteoblastsen_US
dc.subjectOsteogenesisen_US
dc.subjectParietal Boneen_US
dc.subjectPilot Projectsen_US
dc.subjectProteinsen_US
dc.subjectProteomeen_US
dc.subjectProteomicsen_US
dc.subjectRabbitsen_US
dc.subjectSurface Propertiesen_US
dc.subjectTitaniumen_US
dc.subjectWound Healingen_US
dc.titleProtein expression during early stages of bone regeneration under hydrophobic and hydrophilic titanium domes. A pilot study.en_US
dc.typeArticle
dc.rights.holder© 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
dc.identifier.doi10.1111/jre.12498en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/29063586en_US
pubs.issue2en_US
pubs.notes12 monthsen_US
pubs.publication-statusPublisheden_US
pubs.volume53en_US
dcterms.dateAccepted2017-08-13en_US


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