Yan Xu, Wu Zhou, Wang Biyao, Yu Tianhao, Hu Yue, Wang Sijian, Deng Chunfu, Zhao Baohong, Nakanishi Hiroshi, Zhang Xinwen
The VIP Department, School and Hospital of Stomatology, China Medical University, Liaoning Provincial Key Laboratory of Oral Diseases, Shenyang 110002, China.
Department of Aging Science and Pharmacology, Faculty of Dental Science, Kyushu University, Fukuoka 812-8582, Japan.
Evid Based Complement Alternat Med. 2020 Mar 31;2020:4517587. doi: 10.1155/2020/4517587. eCollection 2020.
Periodontitis is an infectious disease whereby the chronic inflammatory process of the periodontium stimulated by bacterial products induces specific host cell responses. The activation of the host cell immune system upregulates the production of inflammatory mediators, comprising cytokines and proteolytic enzymes, which contribute to inflammation and bone destruction. It has been well known that periodontitis is related to systemic inflammation which links to numerous systemic diseases, including diabetes and arteriosclerosis. Furthermore, periodontitis has been reported in association with neurodegenerative diseases such as Alzheimer's disease (AD) in the brain. Regarding immune responses and inflammation, cathepsin B (CatB) plays pivotal role for the induction of IL-1, cathepsin K- (CatK-) dependent active toll-like receptor 9 (TLR9) signaling, and cathepsin S (CatS) which involves in regulating both TLR signaling and maturation of the MHC class II complex. Notably, both the production and proteolytic activities of cathepsins are upregulated in chronic inflammatory diseases, including periodontitis. In the present review, we focus on the roles of cathepsins in the innate and adaptive immune responses within periodontitis. We believe that understanding the roles of cathepsins in the immune responses in periodontitis would help to elucidate the therapeutic strategies of periodontitis, thus benefit for reduction of systemic diseases as well as neurodegenerative diseases in the global aging society.
牙周炎是一种感染性疾病,细菌产物刺激牙周组织引发慢性炎症过程,进而诱导宿主细胞产生特定反应。宿主细胞免疫系统的激活会上调炎症介质的产生,这些炎症介质包括细胞因子和蛋白水解酶,它们会加剧炎症和骨质破坏。众所周知,牙周炎与全身炎症相关,而全身炎症又与包括糖尿病和动脉硬化在内的多种全身性疾病有关。此外,据报道牙周炎还与大脑中的神经退行性疾病如阿尔茨海默病(AD)有关。在免疫反应和炎症方面,组织蛋白酶B(CatB)在诱导白细胞介素-1、组织蛋白酶K(CatK)依赖的活性Toll样受体9(TLR9)信号传导以及参与调节TLR信号传导和MHC II类复合物成熟的组织蛋白酶S(CatS)中起关键作用。值得注意的是,在包括牙周炎在内的慢性炎症性疾病中,组织蛋白酶的产生和蛋白水解活性均会上调。在本综述中,我们重点关注组织蛋白酶在牙周炎的固有免疫和适应性免疫反应中的作用。我们认为,了解组织蛋白酶在牙周炎免疫反应中的作用将有助于阐明牙周炎的治疗策略,从而有益于在全球老龄化社会中减少全身性疾病和神经退行性疾病。