Publication:
Titanium Surface Characteristics Induce the Specific Reprogramming of Toll-like Receptor Signaling in Macrophages.

dc.contributor.authorGonzález-Sánchez, Zaira
dc.contributor.authorAreal-Quecuty, Victoria
dc.contributor.authorJimenez-Guerra, Alvaro
dc.contributor.authorCabanillas-Balsera, Daniel
dc.contributor.authorGil, Francisco Javier
dc.contributor.authorVelasco-Ortega, Eugenio
dc.contributor.authorPozo, David
dc.date.accessioned2023-05-03T14:01:05Z
dc.date.available2023-05-03T14:01:05Z
dc.date.issued2022-04-13
dc.description.abstractMost of the research on titanium-based dental implants (Ti-discs) is focused on how they are able to stimulate the formation of new tissue and/or cytotoxic studies, with very scarce data on their effects on functional responses by immunocompetent cells. In particular, the link between the rewiring of innate immune responses and surface biomaterials properties is poorly understood. To address this, we characterize the functional response of macrophage cultures to four different dental titanium surfaces (MA: mechanical abrasion; SB + AE: sandblasting plus etching; SB: sandblasting; AE: acid etching). We use different Toll-like receptor (TLR) ligands towards cell surface receptors (bacterial lipopolysaccharide LPS for TLR4; imiquimod for TLR7; synthetic bacterial triacylated lipoprotein for TLR2/TLR1) and endosomal membrane receptor (poly I:C for TLR3) to simulate bacterial (cell wall bacterial components) or viral infections (dsRNA and ssRNA). The extracellular and total LDH levels indicate that exposure to the different Ti-surfaces is not cytotoxic for macrophages under resting or TLR-stimulated conditions, although there is a tendency towards an impairment in macrophage proliferation, viability or adhesion under TLR4, TLR3 and TLR2/1 stimulations in SB discs cultures. The secreted IL-6 and IL-10 levels are not modified upon resting macrophage exposure to the Ti-surfaces studied as well as steady state levels of iNos or ArgI mRNA. However, macrophage exposure to MA Ti-surface do display an enhanced immune response to TLR4, TLR7 or TLR2/1 compared to other Ti-surfaces in terms of soluble immune mediators secreted and M1/M2 gene expression profiling. This change of characteristics in cellular phenotype might be related to changes in cellular morphology. Remarkably, the gene expression of Tlr3 is the only TLR that is differentially affected by distinct Ti-surface exposure. These results highlight the relevance of patterned substrates in dental implants to achieve a smart manipulation of the immune responses in the context of personalized medicine, cell-based therapies, preferential lineage commitment of precursor cells or control of tissue architecture in oral biology.
dc.identifier.doi10.3390/ijms23084285
dc.identifier.essn1422-0067
dc.identifier.pmcPMC9030374
dc.identifier.pmid35457102
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9030374/pdf
dc.identifier.unpaywallURLhttps://www.mdpi.com/1422-0067/23/8/4285/pdf?version=1649833226
dc.identifier.urihttp://hdl.handle.net/10668/21150
dc.issue.number8
dc.journal.titleInternational journal of molecular sciences
dc.journal.titleabbreviationInt J Mol Sci
dc.language.isoen
dc.organizationCentro Andaluz de Biología Molecular y Medicina Regenerativa-CABIMER
dc.pubmedtypeJournal Article
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectToll-like receptors
dc.subjectdental implants
dc.subjectimmune regulation
dc.subjectmacrophage cells
dc.subjectsurfaces
dc.subjecttitanium discs
dc.subject.meshCells, Cultured
dc.subject.meshDental Implants
dc.subject.meshLipopolysaccharides
dc.subject.meshMacrophages
dc.subject.meshTitanium
dc.subject.meshToll-Like Receptor 2
dc.subject.meshToll-Like Receptor 3
dc.subject.meshToll-Like Receptor 4
dc.subject.meshToll-Like Receptor 7
dc.subject.meshToll-Like Receptor 9
dc.subject.meshToll-Like Receptors
dc.titleTitanium Surface Characteristics Induce the Specific Reprogramming of Toll-like Receptor Signaling in Macrophages.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number23
dspace.entity.typePublication

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