Leukotriene B4 Loaded in Microspheres Inhibits Osteoclast Differentiation and Activation.
Francine Lorencetti SilvaMaya Fernanda Manfrin ArnezJoão Pedro de Queiroz ThoméMarcio Santos de CarvalhoFabrício Kitazono de CarvalhoAlexandra Mussolino de QueirozLúcia Helena FaccioliFrancisco Wanderley Garcia de Paula E SilvaPublished in: Brazilian dental journal (2022)
To investigate osteoclast formation in vivo and if leukotriene B4 (LTB4) 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, LTB4-MS were prepared using an oil-in-water emulsion solvent extraction-evaporation process. Characterization and efficiency of LTB4 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 LTB4-MS. Cytotoxicity, in vitro MS-LTB4 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, LTB4-MS were up-taken by macrophages and were not cytotoxic to the cells. LTB4-MS inhibited osteoclast formation and the synthesis of osteoclastogenic genes Acp5, Mmp9, Calcr and Ctsk. LTB4-MS inhibited differentiation of macrophages into an osteoclastic phenotype and cell activation under M-CSF and RANKL stimulus.
Keyphrases
- nuclear factor
- mass spectrometry
- multiple sclerosis
- ms ms
- bone loss
- gene expression
- toll like receptor
- dna methylation
- endothelial cells
- high resolution
- oxidative stress
- cancer therapy
- dendritic cells
- metabolic syndrome
- liquid chromatography
- genome wide
- skeletal muscle
- single cell
- adipose tissue
- mesenchymal stem cells
- cell proliferation
- signaling pathway
- insulin resistance
- cell cycle arrest
- ionic liquid
- high speed
- molecularly imprinted
- tandem mass spectrometry