Comparison of the response of cultured osteoblasts and osteoblasts outgrown from rat calvarial bone chips to nonfouling KRSR and FHRRIKA‐peptide modified rough titanium surfaces

dc.contributor.authorSchuler, Martin
dc.contributor.authorHamilton, Douglas W.
dc.contributor.authorKunzler, Tobias P.
dc.contributor.authorSprecher, Christoph M.
dc.contributor.authorde Wild, Michael
dc.contributor.authorBrunette, Donald M.
dc.contributor.authorTextor, Marcus
dc.contributor.authorTosatti, Samuele G. P.
dc.date.accessioned2024-05-15T08:34:56Z
dc.date.available2024-05-15T08:34:56Z
dc.date.issued2009-11
dc.description.abstractMimicking proteins found in the extracellular matrix (ECM) using specific peptide sequences is a well-known strategy for the design of biomimetic surfaces, but has not yet been widely exploited in the field of biomedical implants. This study investigated osteoblast and, as a control, fibroblast proliferation to novel consensus heparin-binding peptides sequences KRSR and FHRIKKA that were immobilized onto rough (particle-blasted and chemically etched) commercially pure titanium surfaces using a poly(L-lysine)-graft- poly(ethylene glycol) (PLL-g-PEG) molecular assembly system. This platform enabled a detailed study of specific cell-peptide interactions even in the presence of serum in the culture medium; thanks to the excellent nonfouling properties of the PLL-g-PEG surface. Cell-binding peptide sequence RGD in combination with KRSR or FHRRIKA was used to examine a potentially-enhanced or synergistic effect on osteoblast proliferation. Bare titanium and bioinactive surfaces (i.e., unfunctionalized PLL-g-PEG and scrambled KSSR, RFHARIK, and RDG) were used as control substrates. Additionally, in a newly developed experimental setup, freshly harvested bone chips from newborn rat calvariae were placed onto the same type of surfaces investigating size and pattern of osteoblast outgrowths. The findings of the current study demonstrated that the difference in osteoblast and fibroblast proliferation was influenced by surface topography more so than by the presence of surface-bound KRSR and FHRRIKA. On the other hand, in comparison with the control surfaces, osteoblast outgrowths from rat calvarial bone chips covered a significantly larger area on RGD, KRSR, and FHRRIKA surfaces after 8 days and also migrated in an isotropic way unlike cells on the bioinactive substrates. Furthermore, the stimulatory effect of 0.75 pmol cm-2 RGD on osteoblast migration pattern could be enhanced when applied in combination with 2.25 pmol cm-2 KRSR.
dc.identifier.doi10.1002/jbm.b.31425
dc.identifier.issn1552-4973
dc.identifier.issn1552-4981
dc.identifier.urihttps://irf.fhnw.ch/handle/11654/45807
dc.issue2
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofJournal of Biomedical Materials Research Part B: Applied Biomaterials
dc.subjectBiomimetic
dc.subjectHuman gingival fibroblasts
dc.subjectPrimary rat calvarial osteoblasts
dc.subjectSurface (bio)chemistry
dc.subjectSurface topography
dc.subject.ddc600 - Technik, Medizin, angewandte Wissenschaften
dc.titleComparison of the response of cultured osteoblasts and osteoblasts outgrown from rat calvarial bone chips to nonfouling KRSR and FHRRIKA‐peptide modified rough titanium surfaces
dc.type01A - Beitrag in wissenschaftlicher Zeitschrift
dc.volume91B
dspace.entity.typePublication
fhnw.InventedHereNo
fhnw.ReviewTypeAnonymous ex ante peer review of a complete publication
fhnw.affiliation.hochschuleHochschule für Life Sciencesde_CH
fhnw.affiliation.institutInstitut für Medizintechnik und Medizininformatikde_CH
fhnw.openAccessCategoryClosed
fhnw.pagination517 - 527
fhnw.publicationStatePublished
relation.isAuthorOfPublication135938a9-969d-4ea3-9bb2-7ff1d77554cb
relation.isAuthorOfPublication.latestForDiscovery135938a9-969d-4ea3-9bb2-7ff1d77554cb
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