Hao Liang, Chen Jianwei, Zhu Zheng, Reddy Michael S, Mountz John D, Chen Wei, Li Yi-Ping
Department of Pathology, University of Alabama at Birmingham, Birmingham, AL.
Department of Periodontology, University of Alabama at Birmingham School of Dentistry, Birmingham, AL.
J Periodontol. 2015 Aug;86(8):972-83. doi: 10.1902/jop.2015.140643. Epub 2015 Apr 16.
Periodontitis is a bacteria-induced inflammatory disease mainly affecting periodontal tissues, leading to periodontal inflammation, bone breakdown, and loss of the tooth. The main obstacle for treating periodontitis effectively is the difficulty in finding a target that can inhibit bone loss and inflammation simultaneously. Recent studies showed that cathepsin K (CTSK) might have functions in the immune system besides its role in osteoclasts. Thus, targeting CTSK would have a potential therapeutic effect in both the bone system and the immune system during the progression of periodontitis.
In the current study, a small molecular inhibitor (odanacatib [ODN]) is explored to inhibit the function of CTSK in a bacteria-induced periodontitis mouse model.
The application of ODN decreased the number of osteoclasts, macrophages, and T cells, as well as the expression of Toll-like receptors (TLRs) in the periodontitis lesion area. Furthermore, lack of CTSK inhibited the expression of TLR4, TLR5, and TLR9 and their downstream cytokine signaling in the gingival epithelial cells in periodontitis lesions, demonstrating that the innate immune response was inhibited in periodontitis.
The present results show that inhibition of CTSK can prevent bone loss and the immune response during the progression of periodontitis, indicating that CTSK is a promising target for treating inflammatory diseases such as periodontitis by affecting both osteoclasts and the immune system.
牙周炎是一种主要影响牙周组织的细菌诱导性炎症性疾病,会导致牙周炎症、骨质破坏和牙齿脱落。有效治疗牙周炎的主要障碍在于难以找到一个能同时抑制骨质流失和炎症的靶点。最近的研究表明,组织蛋白酶K(CTSK)除了在破骨细胞中发挥作用外,可能在免疫系统中也有功能。因此,在牙周炎进展过程中,靶向CTSK可能在骨骼系统和免疫系统中都具有潜在的治疗效果。
在本研究中,探索了一种小分子抑制剂(odanacatib [ODN])在细菌诱导的牙周炎小鼠模型中抑制CTSK的功能。
ODN的应用减少了破骨细胞、巨噬细胞和T细胞的数量,以及牙周炎病变区域中Toll样受体(TLRs)的表达。此外,缺乏CTSK抑制了牙周炎病变牙龈上皮细胞中TLR4、TLR5和TLR9及其下游细胞因子信号的表达,表明牙周炎中的固有免疫反应受到抑制。
目前的结果表明,抑制CTSK可以预防牙周炎进展过程中的骨质流失和免疫反应,这表明CTSK是通过影响破骨细胞和免疫系统来治疗牙周炎等炎症性疾病的一个有前景的靶点。