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dc.contributor.authorMengatto, Cristiane Machadopt_BR
dc.contributor.authorMussano, Federicopt_BR
dc.contributor.authorHonda, Yoshitomopt_BR
dc.contributor.authorColwell, Chistopher S.pt_BR
dc.date.accessioned2021-08-06T04:40:36Zpt_BR
dc.date.issued2011pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/225235pt_BR
dc.description.abstractBackground: Successful dental and orthopedic implants require the establishment of an intimate association with bone tissue; however, the mechanistic explanation of how biological systems accomplish osseointegration is still incomplete. We sought to identify critical gene networks involved in osseointegration by exploring the implant failure model under vitamin D deficiency. Methodology: Adult male Sprague-Dawley rats were exposed to control or vitamin D-deficient diet prior to the osteotomy surgery in the femur bone and the placement of T-shaped Ti4Al6V implant. Two weeks after the osteotomy and implant placement, tissue formed at the osteotomy site or in the hollow chamber of T-shaped implant was harvested and total RNA was evaluated by whole genome microarray analyses. Principal Findings: Two-way ANOVA of microarray data identified 103 genes that were significantly (.2 fold) modulated by the implant placement and vitamin D deficiency. Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses assigned the highest z-score to the circadian rhythm pathway including neuronal PAS domain 2 (NPAS2), and period homolog 2 (Per2). NPAS2 and Aryl hydrocarbon receptor nuclear translocator-like (ARNTL/Bmal 1) were upregulated around implant and diminished by vitamin D deficiency, whereas the expression pattern of Per2 was complementary. Hierarchical cluster analysis further revealed that NPAS2 was in a group predominantly composed of cartilage extracellular matrix (ECM) genes. Whereas the expression of bone ECM genes around implant was not significantly affected by vitamin D deficiency, cartilage ECM genes were modulated by the presence of the implant and vitamin D status. In a proof-of-concept in vitro study, the expression of cartilage type II and X collagens was found upregulated when mouse mesenchymal stem cells were cultured on implant disk with 1,25D supplementation. Conclusions: This study suggests that the circadian rhythm system and cartilage extracellular matrix may be involved in the establishment of osseointegration under vitamin D regulation.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofPLoS ONE [recurso eletrônico]. São Francisco, CA. Vol. 6, no. 1 (Jan. 2011), p. e15848pt_BR
dc.rightsOpen Accessen
dc.subjectOsseointegraçãopt_BR
dc.titleCircadian rhythm and cartilage extracellular matrix genes in osseointegration : a genome-wide screening of implant failure by vitamin D deficiencypt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb000787075pt_BR
dc.type.originEstrangeiropt_BR


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