CCR2型
骨重建
炎症
牙槽
巨噬细胞
细胞生物学
转录组
肺泡巨噬细胞
免疫学
生物
趋化因子
基因
医学
基因表达
牙科
内分泌学
遗传学
趋化因子受体
体外
作者
Hao Xu,Shuting Zhang,Adwait Amod Sathe,Zhichun Jin,Jiani Guan,Wen Sun,Chao Xing,Hanwen Zhang,Bin Yan
标识
DOI:10.3389/fimmu.2022.835986
摘要
During mechanical force-induced alveolar bone remodeling, macrophage-mediated local inflammation plays a critical role. Yet, the detailed heterogeneity of macrophages is still unknown. Single-cell RNA sequencing was used to study the transcriptome heterogeneity of macrophages during alveolar bone remodeling. We identified macrophage subclusters with specific gene expression profiles and functions. CellChat and trajectory analysis revealed a central role of the Ccr2 cluster during development, with the CCL signaling pathway playing a crucial role. We further demonstrated that the Ccr2 cluster modulated bone remodeling associated inflammation through an NF-κB dependent pathway. Blocking CCR2 could significantly reduce the Orthodontic tooth movement (OTM) progression. In addition, we confirmed the variation of CCR2 + macrophages in human periodontal tissues. Our findings reveal that mechanical force-induced functional shift of the Ccr2 macrophages cluster mediated by NF-κB pathway, leading to a pro-inflammatory response and bone remodeling. This macrophage cluster may represent a potential target for the manipulation of OTM.
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