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Publicação:
Titanium-Enriched Medium Promotes Environment-Induced Epigenetic Machinery Changes in Human Endothelial Cells

dc.contributor.authorFernandes, Célio Júnior da C. [UNESP]
dc.contributor.authorda Silva, Rodrigo A. Foganholi
dc.contributor.authorWood, Patrícia F. [UNESP]
dc.contributor.authorFerreira, Marcel Rodrigues [UNESP]
dc.contributor.authorde Almeida, Gerson S. [UNESP]
dc.contributor.authorde Moraes, Julia Ferreira [UNESP]
dc.contributor.authorBezerra, Fábio J. [UNESP]
dc.contributor.authorZambuzzi, Willian F. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversity of Taubaté
dc.contributor.institutionPaulista University
dc.date.accessioned2023-07-29T12:58:09Z
dc.date.available2023-07-29T12:58:09Z
dc.date.issued2023-03-01
dc.description.abstractIt is important to understand whether endothelial cells are epigenetically affected by titanium-enriched media when angiogenesis is required during bone development and it is expected to be recapitulated during osseointegration of biomaterials. To better address this issue, titanium-enriched medium was obtained from incubation of titanium discs for up to 24 h as recommended by ISO 10993-5:2016, and further used to expose human umbilical vein endothelial cells (HUVECs) for up to 72 h, when the samples were properly harvested to allow molecular analysis and epigenetics. In general, our data show an important repertoire of epigenetic players in endothelial cells responding to titanium, reinforcing protein related to the metabolism of acetyl and methyl groups, as follows: Histone deacetylases (HDACs) and NAD-dependent deacetylase sirtuin-1 (Sirt1), DNA methyltransferases (DNMTs) and ten-eleven translocation (TET) methylcytosine dioxygenases, which in conjunction culminate in driving chromatin condensation and the methylation profile of DNA strands, respectively. Taking our data into consideration, HDAC6 emerges as important player of this environment-induced epigenetic mechanism in endothelial cells, while Sirt1 is required in response to stimulation of reactive oxygen species (ROS) production, as its modulation is relevant to vasculature surrounding implanted devices. Collectively, all these findings support the hypothesis that titanium keeps the surrounding microenvironment dynamically active and so affects the performance of endothelial cells by modulating epigenetics. Specifically, this study shows the relevance of HDAC6 as a player in this process, possibly correlated with the cytoskeleton rearrangement of those cells. Furthermore, as those enzymes are druggable, it opens new perspectives to consider the use of small molecules to modulate their activities as a biotechnological tool in order to improve angiogenesis and accelerate bone growth with benefits of a fast recovery time for patients.en
dc.description.affiliationLaboratory of Bioassays and Cellular Dynamics Department of Chemical and Biological Sciences Institute of Biosciences UNESP—São Paulo State University, SP
dc.description.affiliationDepartment of Dentistry University of Taubaté, SP
dc.description.affiliationProgram in Environmental and Experimental Pathology Paulista University, SP
dc.description.affiliationUnespLaboratory of Bioassays and Cellular Dynamics Department of Chemical and Biological Sciences Institute of Biosciences UNESP—São Paulo State University, SP
dc.identifierhttp://dx.doi.org/10.3390/jfb14030131
dc.identifier.citationJournal of Functional Biomaterials, v. 14, n. 3, 2023.
dc.identifier.doi10.3390/jfb14030131
dc.identifier.issn2079-4983
dc.identifier.scopus2-s2.0-85151148643
dc.identifier.urihttp://hdl.handle.net/11449/247066
dc.language.isoeng
dc.relation.ispartofJournal of Functional Biomaterials
dc.sourceScopus
dc.subjectangiogenesis
dc.subjectbiological analysis
dc.subjectbiomaterial
dc.subjectendothelial cell
dc.subjectepigenetic
dc.subjecttitanium
dc.titleTitanium-Enriched Medium Promotes Environment-Induced Epigenetic Machinery Changes in Human Endothelial Cellsen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0002-7754-1855[2]
unesp.author.orcid0000-0002-3445-0945[4]
unesp.author.orcid0000-0002-0208-0441[5]
unesp.author.orcid0000-0002-4149-5965[8]

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