Department of Pathophysiology-Periodontal Science, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Department of Pharmacology, Okayama University Graduate School of Medicine, Dentistry and Pharmacological Sciences, Okayama, Japan.
J Cell Biochem. 2018 Jul;119(7):5481-5490. doi: 10.1002/jcb.26710. Epub 2018 Mar 14.
High mobility group box 1 (HMGB1) is a non-histone DNA-binding protein that is secreted into the extracellular milieu in response to inflammatory stimuli. The secreted HMGB1 has been suggested to mediate various inflammatory diseases. However, it is still unknown whether HMGB1 is involved in a healing process in the tooth extraction socket, the tissue containing gingival epithelium, and alveolar bone that is exposed to oral bacteria. In this study, we constructed a murine tooth extraction model with anti-HMGB1 neutralization antibody administration and observed the inflammatory response and bone healing process in tooth extraction sockets by molecular imaging of myeloperoxidase (MPO) activity, histological analysis, and quantitative RT-PCR. The translocation of HMGB1 from the nucleus to the cytoplasm in gingival epithelial cells and inflammatory cells was inhibited by anti-HMGB1 antibody administration. The MPO activity around the tooth extraction socket was significantly reduced, and the numbers of CD31- and CD68-positive cells were significantly lower in the anti-HMGB1 antibody treatment samples than in the control samples. The TRAP-positive cells, osteocalcin positive cells, and the neoplastic bone area were significantly lower in anti-HMGB1 antibody treatment samples than in control samples. The expression levels of IL-1β and VEGF-A were also decreased in anti-HMGB1 antibody treatment samples compared to that in control samples. Secreted HMGB1 induced initial acute inflammation and inflammatory cells recruitment after tooth extraction. HMGB1 was associated with angiogenesis and bone remodeling by osteoclast and osteoblast activation and promoted bone healing in the tooth extraction socket.
高迁移率族蛋白 B1(HMGB1)是一种非组蛋白 DNA 结合蛋白,在受到炎症刺激时会被分泌到细胞外环境中。已提出分泌的 HMGB1 介导各种炎症性疾病。然而,目前尚不清楚 HMGB1 是否参与拔牙窝(含有牙龈上皮和暴露于口腔细菌的牙槽骨的组织)中的愈合过程。在这项研究中,我们构建了一种抗 HMGB1 中和抗体给药的小鼠拔牙模型,并通过髓过氧化物酶(MPO)活性、组织学分析和定量 RT-PCR 的分子成像观察拔牙窝中的炎症反应和骨愈合过程。牙龈上皮细胞和炎症细胞中 HMGB1 从核到细胞质的易位被抗 HMGB1 抗体给药抑制。牙拔除窝周围的 MPO 活性显著降低,抗 HMGB1 抗体处理样本中的 CD31-和 CD68-阳性细胞数量明显低于对照组。TRAP 阳性细胞、骨钙素阳性细胞和新骨面积在抗 HMGB1 抗体处理样本中明显低于对照组。与对照组相比,抗 HMGB1 抗体处理样本中 IL-1β 和 VEGF-A 的表达水平也降低。分泌的 HMGB1 在拔牙后诱导初始急性炎症和炎症细胞募集。HMGB1 通过破骨细胞和成骨细胞的激活与血管生成和骨重塑有关,并促进拔牙窝中的骨愈合。