微球负载白三烯B4抑制破骨细胞分化和活化

Q2 Medicine
Francine Lorencetti-Silva, Maya Fernanda Manfrin Arnez, João Pedro de Queiroz Thomé, Marcio Santos de Carvalho, Fabrício Kitazono de Carvalho, Alexandra Mussolino de Queiroz, Lúcia Helena Faccioli, Francisco Wanderley Garcia Paula-Silva
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引用次数: 0

摘要

摘要研究体内破骨细胞的形成,以及微球(MS)中负载的白三烯B4(LTB4)是否可以用作促进介质持续递送和防止破骨细胞分化的治疗策略。方法:在体内诱导小鼠根尖周炎,以研究在缺乏5-脂氧合酶(5-LO)的情况下破骨细胞的分化和信号传导。在体外,使用水包油乳液溶剂萃取蒸发工艺制备LTB4-MS。研究了LTB4包封的特性和包封效率。J774A.1巨噬细胞在单核细胞集落刺激因子(M-CSF)和核因子κB受体激活剂配体(RANKL)存在下培养,然后用LTB4-MS刺激。测定细胞毒性、体外MS-LTB4摄取、破骨细胞形成和基因表达。结果:我们发现5-LO在根尖周炎发展过程中对体内破骨细胞的形成具有负调控作用。在体外,LTB4-MS被巨噬细胞吸收,对细胞没有细胞毒性。LTB4-MS抑制破骨细胞的形成和破骨基因Acp5、Mmp9、Calcr和Ctsk的合成。LTB4-MS在M-CSF和RANKL刺激下抑制巨噬细胞向破骨细胞表型的分化和细胞活化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Leukotriene B4 Loaded in Microspheres Inhibits Osteoclast Differentiation and Activation.

Leukotriene B4 Loaded in Microspheres Inhibits Osteoclast Differentiation and Activation.

Leukotriene B4 Loaded in Microspheres Inhibits Osteoclast Differentiation and Activation.

Leukotriene B4 Loaded in Microspheres Inhibits Osteoclast Differentiation and Activation.

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.

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来源期刊
Brazilian dental journal
Brazilian dental journal Dentistry-Dentistry (all)
CiteScore
2.20
自引率
0.00%
发文量
69
审稿时长
12 weeks
期刊介绍: Brazilian Dental Journal, publishes Full-Length Papers, Short Communications and Case Reports, dealing with dentistry or related disciplines and edited six times a year.
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