Single-Cell Atlas of Immune Microenvironment in Orthodontic Tooth Movement

IF 5.7 1区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
J. Wang, C. Tao, H. Liu, Y. Yang, Y. Zhao, K. Tan, F. Chen, E. Yang, Y. Huang, W. Li
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引用次数: 0

Abstract

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 C3ar1 + 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.
正畸牙齿运动免疫微环境单细胞图谱
正畸治疗依赖于牙周组织重塑。虽然已经发现免疫系统调节这一过程,但以前的研究主要集中在常规免疫细胞群的静态分子变化上。最近的一项研究使用单细胞RNA测序(scRNA-seq)分析了正畸牙齿运动(OTM)下的巨噬细胞,引入了新的亚群和功能。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,我们对小鼠进行scRNA-seq,旨在更全面地描述OTM期间的免疫景观,同时以更高的分辨率进一步探索免疫细胞的动态变化、功能和细胞相互作用。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活化。scRNA-seq分析鉴定出7种细胞系和18种主要细胞类型,其中免疫细胞占最大比例。选择单核细胞、粒细胞和淋巴细胞进行个体聚类,然后分析OTM期间特异性基因表达、功能富集和分布变化。伪时间分析应用于单核细胞和粒细胞。我们确定了单核细胞向树突状细胞、不同亚群巨噬细胞和破骨细胞的4种发育途径。在OTM期间,单核细胞倾向于分化。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期间的细胞相互作用,揭示了巨噬细胞向破骨细胞传递的信号增强,特别是在Ccl、Tnf和Spp1途径中。我们发现C3ar1 +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的正调控中,表明其对破骨细胞活性具有正调控作用。总之,本研究揭示了OTM过程中复杂的免疫微环境,为多种免疫细胞类型、它们的特定功能和细胞相互作用提供了详细的视角。
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来源期刊
Journal of Dental Research
Journal of Dental Research 医学-牙科与口腔外科
CiteScore
15.30
自引率
3.90%
发文量
155
审稿时长
3-8 weeks
期刊介绍: The Journal of Dental Research (JDR) is a peer-reviewed scientific journal committed to sharing new knowledge and information on all sciences related to dentistry and the oral cavity, covering health and disease. With monthly publications, JDR ensures timely communication of the latest research to the oral and dental community.
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