Show simple item record

NF-kappa B decoy oligodeoxynucleotide mitigates wear particle-associated bone loss in the murine continuous infusion model

Authordc.contributor.authorLin, Tzu-hua 
Authordc.contributor.authorPajarinen, Jukka 
Authordc.contributor.authorSato, Taishi 
Authordc.contributor.authorLoi, Florence 
Authordc.contributor.authorFan, Changchun 
Authordc.contributor.authorCórdova Jara, Luis 
Authordc.contributor.authorNabeshima, Akira 
Authordc.contributor.authorGibon, Emmanuel 
Authordc.contributor.authorZhang, Ruth 
Authordc.contributor.authorYao, Zhenyu 
Authordc.contributor.authorGoodman, Stuart 
Admission datedc.date.accessioned2016-12-27T20:15:42Z
Available datedc.date.available2016-12-27T20:15:42Z
Publication datedc.date.issued2016
Cita de ítemdc.identifier.citationActa Biomaterialia 41 (2016) 273–281es_ES
Identifierdc.identifier.other10.1016/j.actbio.2016.05.038
Identifierdc.identifier.urihttp://repositorio.uchile.cl/handle/2250/142141
Abstractdc.description.abstractTotal joint replacement is a cost-effective surgical procedure for patients with end-stage arthritis. Wear particle-induced chronic inflammation is associated with the development of periprosthetic osteolysis. Modulation of NF-kappa B signaling in macrophages, osteoclasts, and mesenchymal stem cells could potentially mitigate this disease. In the current study, we examined the effects of local delivery of decoy NF-kappa B oligo-deoxynucleotide (ODN) on wear particle-induced bone loss in a murine continuous femoral particle infusion model. Ultra-high molecular weight polyethylene particles (UHMWPE) with or without lipopolysaccharide (LPS) were infused via osmotic pumps into hollow titanium rods placed in the distal femur of mice for 4 weeks. Particle-induced bone loss was evaluated by IICT, and immunohistochemical analysis of sections from the femur. Particle infusion alone resulted in reduced bone mineral density and trabecular bone volume fraction in the distal femur. The decoy ODN reversed the particle-associated bone volume fraction loss around the implant, irrespective of the presence of LPS. Particle-infusion with LPS increased bone mineral density in the distal femur compared with particle-infusion alone. NF-kappa B decoy ODN reversed or further increased the bone mineral density in the femur (3-6 mm from the distal end) exposed to particles alone or particles plus LPS. NF-kappa B decoy ODN also inhibited macrophage infiltration and osteoclast number, but had no significant effects on osteoblast numbers in femurs exposed to wear particles and LPS. Our study suggests that targeting NF-kappa B activity via local delivery of decoy ODN has great potential to mitigate wear particle -induced osteolysis.es_ES
Patrocinadordc.description.sponsorshipNIH 2R01AR055650 1R01AR063717 Ellenburg Chair in Surgery at Stanford University Jane and Aatos Erkko foundationes_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherElsevieres_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Sourcedc.sourceActa Biomaterialiaes_ES
Keywordsdc.subjectWear particleses_ES
Keywordsdc.subjectChronic inflammationes_ES
Keywordsdc.subjectNF-kappa B decoy oligodeoxynucleotidees_ES
Keywordsdc.subjectPeriprosthetic osteolysises_ES
Títulodc.titleNF-kappa B decoy oligodeoxynucleotide mitigates wear particle-associated bone loss in the murine continuous infusion modeles_ES
Document typedc.typeArtículo de revistaes_ES
Catalogueruchile.catalogadorlajes_ES
Indexationuchile.indexArtículo de publicación ISIes_ES


Files in this item

Icon

This item appears in the following Collection(s)

Show simple item record

Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile