Implant surface physicochemistry affects keratinocyte hemidesmosome formation

dc.contributor.authorRaptopoulos, Michail
dc.contributor.authorFischer, Nicholas G.
dc.contributor.authorAparicio, Conrado
dc.date.accessioned2023-09-13T10:45:07Z
dc.date.available2023-09-13T10:45:07Z
dc.date.issued2023-01-09
dc.date.updated2023-09-06T09:16:37Z
dc.description.abstractPrevious studies have shown hydrophilic/hydrophobic implant surfaces stimulate/hinder osseointegration. An analogous concept was applied here using common biological functional groups on a model surface to promote oral keratinocytes (OKs) proliferation and hemidesmosomes (HD) to extend implant lifespans through increased soft tissue attachment. However, it is unclear what physicochemistry stimulates HDs. Thus, common biological functional groups (NH2 , OH, and CH3 ) were functionalized on glass using silanization. Non-functionalized plasma-cleaned glass and H silanization were controls. Surface modifications were confirmed with X-ray photoelectron spectroscopy and water contact angle. The amount of bovine serum albumin (BSA) and fibrinogen, and BSA thickness, were assessed to understand how adsorbed protein properties were influenced by physicochemistry and may influence HDs. OKs proliferation was measured, and HDs were quantified with immunofluorescence for collagen XVII and integrin β4. Plasma-cleaned surfaces were the most hydrophilic group overall, while CH3 was the most hydrophobic and OH was the most hydrophilic among functionalized groups. Modification with the OH chemical group showed the highest OKs proliferation and HD expression. The OKs response on OH surfaces appeared to not correlate to the amount or thickness of adsorbed model proteins. These results reveal relevant surface physicochemical features to favor HDs and improve implant soft tissue attachment.© 2023 The Authors. Journal of Biomedical Materials Research Part A published by Wiley Periodicals LLC.
dc.format.extent10 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idimarina6573892
dc.identifier.issn1097-4636
dc.identifier.pmid36621832
dc.identifier.urihttps://hdl.handle.net/2445/201873
dc.language.isoeng
dc.publisherWiley
dc.relation.isformatofhttps://doi.org/10.1002/jbm.a.37486
dc.relation.ispartofJournal Of Biomedical Materials Research Part a, 2023, vol. 111, num. 7, p. 1021-1030
dc.relation.urihttps://doi.org/10.1002/jbm.a.37486
dc.rightscc by-nc-nd (c) Raptopoulos, Michail et al., 2023
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.sourceArticles publicats en revistes (Institut de Bioenginyeria de Catalunya (IBEC))
dc.subject.classificationImplants artificials
dc.subject.classificationRebuig (Biologia)
dc.subject.classificationQuímica física
dc.subject.otherArtificial implants
dc.subject.otherGraft rejection
dc.subject.otherPhysical and theoretical chemistry
dc.titleImplant surface physicochemistry affects keratinocyte hemidesmosome formation
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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