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本文引用的文献

1
TLR2 promoter hypermethylation creates innate immune dysbiosis.Toll样受体2启动子高甲基化导致先天性免疫失调。
J Dent Res. 2015 Jan;94(1):183-91. doi: 10.1177/0022034514557545. Epub 2014 Nov 11.
2
Periodontitis-activated monocytes/macrophages cause aortic inflammation.牙周炎激活的单核细胞/巨噬细胞会引发主动脉炎症。
Sci Rep. 2014 Jun 4;4:5171. doi: 10.1038/srep05171.
3
Cbfβ deletion in mice recapitulates cleidocranial dysplasia and reveals multiple functions of Cbfβ required for skeletal development.Cbfβ 缺失的小鼠重现 cleidocranial dysplasia ,揭示了 Cbfβ 在骨骼发育中所需的多种功能。
Proc Natl Acad Sci U S A. 2014 Jun 10;111(23):8482-7. doi: 10.1073/pnas.1310617111. Epub 2014 May 21.
4
Inhibition of Rgs10 Expression Prevents Immune Cell Infiltration in Bacteria-induced Inflammatory Lesions and Osteoclast-mediated Bone Destruction.抑制Rgs10表达可防止细菌诱导的炎症病变中的免疫细胞浸润和破骨细胞介导的骨破坏。
Bone Res. 2013 Sep 1;1(3):267-281. doi: 10.4248/BR201303005.
5
Expression of cathepsin K in periodontitis and in gingival fibroblasts.组织蛋白酶K在牙周炎及牙龈成纤维细胞中的表达
Oral Dis. 2015 Mar;21(2):163-9. doi: 10.1111/odi.12230. Epub 2014 Mar 24.
6
Periodontopathogen profile of healthy and oral lichen planus patients with gingivitis or periodontitis.健康人群、伴龈炎或牙周炎的口腔扁平苔藓患者的牙周病致病菌谱。
Int J Oral Sci. 2013 Jun;5(2):92-7. doi: 10.1038/ijos.2013.30. Epub 2013 Jun 7.
7
C/EBPα regulates osteoclast lineage commitment.C/EBPα 调节破骨细胞谱系的定向分化。
Proc Natl Acad Sci U S A. 2013 Apr 30;110(18):7294-9. doi: 10.1073/pnas.1211383110. Epub 2013 Apr 11.
8
RNAi-mediated silencing of Atp6i and Atp6i haploinsufficiency prevents both bone loss and inflammation in a mouse model of periodontal disease.RNAi 介导的 Atp6i 沉默和 Atp6i 杂合不足可预防牙周病小鼠模型中的骨丢失和炎症。
PLoS One. 2013;8(4):e58599. doi: 10.1371/journal.pone.0058599. Epub 2013 Apr 5.
9
Activation of invariant NK T cells in periodontitis lesions.固有自然杀伤 T 细胞在牙周病病变中的活化。
J Immunol. 2013 Mar 1;190(5):2282-91. doi: 10.4049/jimmunol.1201215. Epub 2013 Jan 30.
10
Cathepsin-mediated necrosis controls the adaptive immune response by Th2 (T helper type 2)-associated adjuvants.组织蛋白酶介导的细胞坏死通过与 Th2(辅助性 T 细胞 2 型)相关佐剂控制适应性免疫反应。
J Biol Chem. 2013 Mar 15;288(11):7481-7491. doi: 10.1074/jbc.M112.400655. Epub 2013 Jan 7.

odanacatib,一种组织蛋白酶K特异性抑制剂,可抑制牙周疾病引起的炎症和骨质流失。

Odanacatib, A Cathepsin K-Specific Inhibitor, Inhibits Inflammation and Bone Loss Caused by Periodontal Diseases.

作者信息

Hao Liang, Chen Jianwei, Zhu Zheng, Reddy Michael S, Mountz John D, Chen Wei, Li Yi-Ping

机构信息

Department of Pathology, University of Alabama at Birmingham, Birmingham, AL.

Department of Periodontology, University of Alabama at Birmingham School of Dentistry, Birmingham, AL.

出版信息

J Periodontol. 2015 Aug;86(8):972-83. doi: 10.1902/jop.2015.140643. Epub 2015 Apr 16.

DOI:10.1902/jop.2015.140643
PMID:25879791
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4648620/
Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

背景

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。

方法

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。

结果

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。

结论

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。