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Leukotriene B(4) Loaded in Microspheres Inhibits Osteoclast Differentiation and Activation

To investigate osteoclast formation in vivo and if leukotriene B(4) (LTB(4)) loaded in microspheres (MS) could be used as a therapeutical strategy to promote a sustained delivery of the mediator and prevent osteoclast differentiation. Methods: In vivo, apical periodontitis was induced in mice to inv...

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Detalles Bibliográficos
Autores principales: Lorencetti-Silva, Francine, Arnez, Maya Fernanda Manfrin, Thomé, João Pedro de Queiroz, de Carvalho, Marcio Santos, de Carvalho, Fabrício Kitazono, de Queiroz, Alexandra Mussolino, Faccioli, Lúcia Helena, Paula-Silva, Francisco Wanderley Garcia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Fundação Odontológica de Ribeirão Preto 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9645171/
https://www.ncbi.nlm.nih.gov/pubmed/36287497
http://dx.doi.org/10.1590/0103-6440202204827
Descripción
Sumario:To investigate osteoclast formation in vivo and if leukotriene B(4) (LTB(4)) loaded in microspheres (MS) could be used as a therapeutical strategy to promote a sustained delivery of the mediator and prevent osteoclast differentiation. Methods: In vivo, apical periodontitis was induced in mice to investigate osteoclast differentiation and signaling in absence of 5-lipoxygenase (5-LO). In vitro, LTB(4)-MS were prepared using an oil-in-water emulsion solvent extraction-evaporation process. Characterization and efficiency of LTB(4) encapsulation were investigated. J774A.1 macrophages were cultured in the presence of monocyte colony-stimulating factor (M-CSF) and ligand for receptor activator of nuclear factor kappa B (RANKL) and then stimulated with LTB(4)-MS. Cytotoxicity, in vitro MS-LTB(4) uptake, osteoclast formation and gene expression were measured. Results: We found that 5-LO negatively regulates osteoclastic formation in vivo during apical periodontitis development. In vitro, LTB(4)-MS were up-taken by macrophages and were not cytotoxic to the cells. LTB(4)-MS inhibited osteoclast formation and the synthesis of osteoclastogenic genes Acp5, Mmp9, Calcr and Ctsk. LTB(4)-MS inhibited differentiation of macrophages into an osteoclastic phenotype and cell activation under M-CSF and RANKL stimulus.