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M1 型巨噬细胞极化促进正畸牙齿移动。

M1-like Macrophage Polarization Promotes Orthodontic Tooth Movement.

作者信息

He D, Kou X, Yang R, Liu D, Wang X, Luo Q, Song Y, Liu F, Yan Y, Gan Y, Zhou Y

机构信息

Department of Orthodontics, Peking University School and Hospital of Stomatology, Beijing, P.R. China Center for Craniofacial Stem Cell Research and Regeneration, Peking University School and Hospital of Stomatology, Beijing, P.R. China.

Center for Temporomandibular Disorders and Orofacial Pain, Peking University School and Hospital of Stomatology, Beijing, P.R. China.

出版信息

J Dent Res. 2015 Sep;94(9):1286-94. doi: 10.1177/0022034515589714. Epub 2015 Jun 29.

Abstract

Macrophages play a crucial role in inflammatory-mediated bone loss. Orthodontic tooth movement (OTM) is associated with inflammatory bone remodeling. However, whether and how macrophages contribute to mechanical force-induced OTM remains unknown. In this study, we hypothesized that polarization of M1-like macrophages may contribute to the OTM. Orthodontic nickel-titanium springs were applied to the upper first molars of rats or mice to induce OTM. The distance of OTM gradually increased after mechanical force was applied to the rats for 5 and 10 d. M1-like macrophage polarization and expression of M1 cytokine tumor necrosis factor (TNF)-α also increased after force application. More importantly, monocyte/macrophage depletion in mice by injection of clodronate liposomes decreased the distance of OTM and the number of tartrate-resistant acid phosphatase (TRAP)-positive osteoclasts and CD68(+) macrophages, accompanied by reduced expressions of M1 markers TNF-α and inducible nitric oxide synthase (iNOS), whereas systemic transfusion of M1 macrophages in mice increased them. Further experiments showed that injection of recombinant TNF-α increased the distance of OTM and the number of TRAP-positive osteoclasts and CD68(+) macrophages, as well as upregulated the expression of TNF-α and iNOS. Blockage of TNF-α by etanercept injection reduced the distance of OTM and the number of TRAP-positive osteoclasts and CD68(+) macrophages, as well as decreased the levels of TNF-α and iNOS. These data suggest that M1-like macrophage polarization promotes alveolar bone resorption and consequent OTM after mechanical force application.

摘要

巨噬细胞在炎症介导的骨质流失中起关键作用。正畸牙齿移动(OTM)与炎症性骨重塑相关。然而,巨噬细胞是否以及如何促成机械力诱导的OTM仍不清楚。在本研究中,我们假设M1样巨噬细胞的极化可能促成OTM。将正畸镍钛弹簧施加于大鼠或小鼠的上颌第一磨牙以诱导OTM。对大鼠施加机械力5天和10天后,OTM的距离逐渐增加。施加力后,M1样巨噬细胞极化和M1细胞因子肿瘤坏死因子(TNF)-α的表达也增加。更重要的是,通过注射氯膦酸盐脂质体使小鼠体内的单核细胞/巨噬细胞耗竭,可减少OTM的距离、抗酒石酸酸性磷酸酶(TRAP)阳性破骨细胞和CD68(+)巨噬细胞的数量,同时伴有M1标志物TNF-α和诱导型一氧化氮合酶(iNOS)表达的降低,而给小鼠全身输注M1巨噬细胞则会增加这些指标。进一步的实验表明,注射重组TNF-α可增加OTM的距离、TRAP阳性破骨细胞和CD68(+)巨噬细胞的数量,并上调TNF-α和iNOS的表达。注射依那西普阻断TNF-α可减少OTM的距离、TRAP阳性破骨细胞和CD68(+)巨噬细胞的数量,并降低TNF-α和iNOS的水平。这些数据表明,M1样巨噬细胞极化促进机械力施加后牙槽骨吸收及随之而来的OTM。

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