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载有白三烯 B4 的微球可抑制破骨细胞分化和激活。

Leukotriene B4 Loaded in Microspheres Inhibits Osteoclast Differentiation and Activation.

机构信息

Departamento de Clínica Infantil, Faculdade de Odontologia de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, São Paulo, Brasil.

Universidade de Rio Verde, Rio Verde, Goiás, Brasil.

出版信息

Braz Dent J. 2022 Sep-Oct;33(5):35-45. doi: 10.1590/0103-6440202204827.

Abstract

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.

摘要

目的

研究体内破骨细胞的形成,以及负载白三烯 B4(LTB4)的微球(MS)是否可用作促进介质持续递送并防止破骨细胞分化的治疗策略。方法:在体内,通过在缺乏 5-脂氧合酶(5-LO)的情况下在小鼠中诱导根尖周炎,以研究破骨细胞分化和信号转导。在体外,使用油包水乳液溶剂萃取蒸发法制备 LTB4-MS。对 LTB4 包封的特性和效率进行了研究。在单核细胞集落刺激因子(M-CSF)和核因子κB 受体激活剂(RANKL)的存在下培养 J774A.1 巨噬细胞,然后用 LTB4-MS 刺激。测量细胞毒性、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负调节体内破骨细胞的形成。在体外,LTB4-MS 被巨噬细胞摄取,对细胞无细胞毒性。LTB4-MS 抑制破骨细胞形成和破骨细胞生成基因 Acp5、Mmp9、Calcr 和 Ctsk 的合成。LTB4-MS 抑制巨噬细胞在 M-CSF 和 RANKL 刺激下向破骨细胞表型分化和细胞激活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3d5/9645171/9b000fa978fd/1806-4760-bdj-33-05-35-gf1.jpg

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