Department of Stomatology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Hubei Province Key Laboratory of Oral and Maxillofacial Development and Regeneration, Wuhan, 430022, China.
J Transl Med. 2020 Dec 11;18(1):479. doi: 10.1186/s12967-020-02664-7.
Periodontitis, a bacterium-induced inflammatory disease that is characterized by alveolar bone loss, is highly prevalent worldwide. Elucidating the underlying mechanisms of alveolar bone loss in periodontitis is crucial for understanding its pathogenesis. Classically, bone cells, such as osteoclasts, osteoblasts and bone marrow stromal cells, are thought to dominate the development of bone destruction in periodontitis. Recently, osteocytes, the cells embedded in the mineral matrix, have gained attention. This review demonstrates the key contributing role of osteocytes in periodontitis, especially in alveolar bone loss. Osteocytes not only initiate physiological bone remodeling but also assist in inflammation-related changes in bone remodeling. The latest evidence suggests that osteocytes are involved in regulating bone anabolism and catabolism in the progression of periodontitis. The altered secretion of receptor activator of NF-κB ligand (RANKL), sclerostin and Dickkopf-related protein 1 (DKK1) by osteocytes affects the balance of bone resorption and formation and promotes bone loss. In addition, the accumulation of prematurely senescent and apoptotic osteocytes observed in alveolar bone may exacerbate local destruction. Based on their communication with the bloodstream, it is noteworthy that osteocytes may participate in the interaction between local periodontitis lesions and systemic diseases. Overall, further investigations of osteocytes may provide vital insights that improve our understanding of the pathophysiology of periodontitis.
牙周炎是一种由细菌引起的炎症性疾病,其特征为牙槽骨丧失,在全球范围内高发。阐明牙周炎中牙槽骨丧失的潜在机制对于理解其发病机制至关重要。传统上,骨细胞,如破骨细胞、成骨细胞和骨髓基质细胞,被认为主导牙周炎中骨破坏的发展。最近,骨细胞,即嵌入在矿化基质中的细胞,引起了关注。本综述展示了骨细胞在牙周炎,特别是牙槽骨丧失中的关键作用。骨细胞不仅启动生理性骨重塑,而且有助于炎症相关的骨重塑改变。最新证据表明,骨细胞参与调节牙周炎进展过程中的骨合成代谢和分解代谢。骨细胞改变分泌核因子-κB 受体激活剂配体 (RANKL)、硬化素和 Dickkopf 相关蛋白 1 (DKK1),影响骨吸收和形成的平衡,促进骨丢失。此外,在牙槽骨中观察到的过早衰老和凋亡的骨细胞的积累可能会加重局部破坏。基于其与血流的通讯,值得注意的是,骨细胞可能参与局部牙周炎病变与全身疾病之间的相互作用。总的来说,对骨细胞的进一步研究可能提供重要的见解,从而加深我们对牙周炎病理生理学的理解。