State Key Laboratory of Military Stomatology, Department of Periodontology, School of Stomatology, National Clinical Research Center for Oral Diseases, Fourth Military Medical University, Xi'an, China.
Oral Dis. 2019 Jan;25(1):265-273. doi: 10.1111/odi.12983. Epub 2018 Oct 12.
Although accumulating evidence indicates that macrophages are central players in the destructive and reparative phases of periodontal disease, their polarization states at different stages of periodontal inflammation remain unclear.
We collected gingival biopsies from patients with chronic periodontitis (P group), gingivitis (G group), or periodontally healthy individuals (H group). Polarized macrophages were identified through immunofluorescence. M1- and M2-related cytokines were detected by immunohistochemistry.
Compared with the H group, the P group had more M1 cells (higher M1/M2 ratio) and significantly higher TNF-α, IFN-γ, IL-6, and IL-12 levels. Although the G group also exhibited higher TNF-α and IL-12 levels than the H group, they had similar M1/M2 ratios. The M1/M2 ratio and IFN-γ and IL-6 levels were significantly higher in the P than the G group. Among M2-related cytokines, IL-4 levels were significantly higher in the G than the H group. The M1/M2 ratio was positively correlated with clinical probing depth (PD), and both were positively correlated with IFN-γ and IL-6. PD was negatively correlated with IL-4.
Macrophage polarization in gingival tissue may be responsible for the development and progression of inflammation-induced tissue destruction, and modulating macrophage function may be a potential strategy for periodontal disease management.
尽管越来越多的证据表明巨噬细胞在牙周病的破坏和修复阶段中起着核心作用,但它们在牙周炎症的不同阶段的极化状态仍不清楚。
我们收集了慢性牙周炎(P 组)、牙龈炎(G 组)或牙周健康个体(H 组)的牙龈活检组织。通过免疫荧光鉴定极化的巨噬细胞。通过免疫组织化学检测 M1 和 M2 相关细胞因子。
与 H 组相比,P 组的 M1 细胞(更高的 M1/M2 比值)更多,TNF-α、IFN-γ、IL-6 和 IL-12 水平显著更高。虽然 G 组的 TNF-α 和 IL-12 水平也高于 H 组,但它们的 M1/M2 比值相似。P 组的 M1/M2 比值、IFN-γ 和 IL-6 水平均显著高于 G 组。在 M2 相关细胞因子中,G 组的 IL-4 水平显著高于 H 组。M1/M2 比值与临床探诊深度(PD)呈正相关,两者均与 IFN-γ 和 IL-6 呈正相关。PD 与 IL-4 呈负相关。
牙龈组织中巨噬细胞的极化可能是炎症引起的组织破坏发展和进展的原因,调节巨噬细胞功能可能是牙周病管理的一种潜在策略。