Wang J, Tao C, Liu H, Yang Y, Zhao Y, Tan K, Chen F, Yang E, Huang Y, Li W
Department of Orthodontics, Peking University School and Hospital of Stomatology & National Center for Stomatology & National Clinical Research Center for Oral Diseases & National Engineering Research Center of Oral Biomaterials and Digital Medical Devices & Beijing Key Laboratory of Digital Stomatology & NHC Key Laboratory of Digital Stomatology & NMPA Key Laboratory for Dental Materials, Beijing, China.
Department of Human Anatomy, Histology and Embryology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.
J Dent Res. 2025 Jun 26:220345251334583. doi: 10.1177/00220345251334583.
Orthodontic treatment depends on periodontal tissue remodeling. While the immune system has been found to regulate this process, previous studies mostly focused on the static molecular changes in conventional immune cell sets. A recent study used single-cell RNA sequencing (scRNA-seq) to analyze macrophages under orthodontic tooth movement (OTM), introducing new subclusters and functions. However, changes in other immune cells and their interactions with surrounding stromal cells are yet unclarified. Therefore, we performed scRNA-seq in mice, aiming to describe a more comprehensive immune landscape during OTM, while further exploring the dynamic changes, functions, and cellular interactions of immune cells at a higher resolution. We first confirmed the dynamic activation of osteoclasts, osteoblasts, and immune cells at various time points. The scRNA-seq analysis identified 7 cell lineages and 18 major cell types, with immune cells forming the largest proportion. Monocytic cells, granulocytes, and lymphocytes were selected for individual reclustering, followed by analysis of specific gene expression, functional enrichment, and distribution changes during OTM. Pseudotime analysis was applied to monocytic cells and granulocytes. We identified 4 developmental pathways in monocytic cells toward dendritic cells, different subsets of macrophages, and osteoclasts. Monocytic cells tended to be more differentiated during OTM. Meanwhile, in granulocytes, neutrophil subclusters were all highly differentiated. Additionally, we assessed the cellular interactions during OTM, revealing enhanced signaling from macrophages toward osteoclasts, especially in Ccl, Tnf, and Spp1 pathways. We identified that the macrophage subcluster expressed these cytokines at a high level and was enriched in positive regulation of the mitogen-activated protein kinase cascade, indicating its positive regulation toward osteoclast activity. In conclusion, this study revealed the complex immune microenvironment during OTM, providing a detailed perspective on the diverse immune cell types, their specific functions, and cellular interactions.
正畸治疗依赖于牙周组织重塑。虽然已发现免疫系统可调节这一过程,但以往研究大多集中在传统免疫细胞群的静态分子变化上。最近一项研究使用单细胞RNA测序(scRNA-seq)分析正畸牙齿移动(OTM)过程中的巨噬细胞,发现了新的亚群和功能。然而,其他免疫细胞的变化及其与周围基质细胞的相互作用尚不清楚。因此,我们在小鼠中进行了scRNA-seq,旨在描绘OTM过程中更全面的免疫图谱,同时以更高分辨率进一步探索免疫细胞的动态变化、功能和细胞间相互作用。我们首先证实了破骨细胞、成骨细胞和免疫细胞在不同时间点的动态激活。scRNA-seq分析确定了7个细胞谱系和18种主要细胞类型,其中免疫细胞占比最大。选择单核细胞、粒细胞和淋巴细胞进行单独聚类,随后分析OTM期间的特定基因表达、功能富集和分布变化。对单核细胞和粒细胞应用了拟时间分析。我们在单核细胞中确定了4条向树突状细胞、不同巨噬细胞亚群和破骨细胞的发育途径。单核细胞在OTM期间倾向于更分化。同时,在粒细胞中,中性粒细胞亚群均高度分化。此外,我们评估了OTM期间的细胞间相互作用,发现巨噬细胞向破骨细胞的信号增强,尤其是在Ccl、Tnf和Spp1途径中。我们确定巨噬细胞亚群高水平表达这些细胞因子,并富集于丝裂原活化蛋白激酶级联反应的正调控中,表明其对破骨细胞活性的正调控作用。总之,本研究揭示了OTM期间复杂的免疫微环境,为多种免疫细胞类型、其特定功能和细胞间相互作用提供了详细视角。