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机械诱导的 M2 型巨噬细胞参与腭扩张过程中鼻中隔缝的骨重塑。

Mechanically induced M2 macrophages are involved in bone remodeling of the midpalatal suture during palatal expansion.

机构信息

Department of Orthodontics, School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong Key Laboratory of Oral Tissue Regeneration & Shandong Engineering Laboratory for Dental Materials and Oral Tissue Regeneration & Shandong Provincial Clinical Research Center for Oral Diseases, Shandong University, No.44-1 Wenhua Road West, Shandong, Jinan, 250012, China.

出版信息

Prog Orthod. 2024 Aug 5;25(1):30. doi: 10.1186/s40510-024-00529-z.

Abstract

BACKGROUND

Palatal expansion is a common way of treating maxillary transverse deficiency. Under mechanical force, the midpalatal suture is expanded, causing local immune responses. This study aimed to determine whether macrophages participate in bone remodeling of the midpalatal suture during palatal expansion and the effects on bone remodeling.

METHODS

Palatal expansion model and macrophage depletion model were established. Micro-CT, histological staining, and immunohistochemical staining were used to investigate the changes in the number and phenotype of macrophages during palatal expansion as well as the effects on bone remodeling of the midpalatal suture. Additionally, the effect of mechanically induced M2 macrophages on palatal osteoblasts was also elucidated in vitro.

RESULTS

The number of macrophages increased significantly and polarized toward M2 phenotype with the increase of the expansion time, which was consistent with the trend of bone remodeling. After macrophage depletion, the function of osteoblasts and bone formation at the midpalatal suture were impaired during palatal expansion. In vitro, conditioned medium derived from M2 macrophages facilitated osteogenic differentiation of osteoblasts and decreased the RANKL/OPG ratio.

CONCLUSIONS

Macrophages through polarizing toward M2 phenotype participated in midpalatal suture bone remodeling during palatal expansion, which may provide a new idea for promoting bone remodeling from the perspective of regulating macrophage polarization.

摘要

背景

腭扩张是治疗上颌横向发育不足的常用方法。在机械力的作用下,腭中缝扩张,引起局部免疫反应。本研究旨在探讨巨噬细胞是否参与腭扩张过程中的腭中缝骨改建及其对骨改建的影响。

方法

建立腭扩张模型和巨噬细胞耗竭模型。采用 micro-CT、组织学染色和免疫组织化学染色技术,研究腭扩张过程中巨噬细胞数量和表型的变化及其对腭中缝骨改建的影响。此外,还在体外阐明了机械诱导的 M2 巨噬细胞对腭成骨细胞的影响。

结果

随着扩张时间的增加,巨噬细胞数量显著增加,并向 M2 表型极化,这与骨改建的趋势一致。在巨噬细胞耗竭后,腭扩张过程中中缝骨的成骨细胞功能和骨形成受损。在体外,M2 巨噬细胞的条件培养基促进了成骨细胞的成骨分化,并降低了 RANKL/OPG 比值。

结论

巨噬细胞通过向 M2 表型极化参与了腭扩张过程中的腭中缝骨改建,这可能为从调节巨噬细胞极化的角度促进骨改建提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ce1/11298508/d5162f7a1a3b/40510_2024_529_Fig1_HTML.jpg

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