Sima Corneliu, Aboodi Guy M, Lakschevitz Flavia S, Sun Chunxiang, Goldberg Michael B, Glogauer Michael
Department of Applied Oral Sciences, The Forsyth Institute, Cambridge, Massachusetts; Department of Oral Medicine, Infection, and Immunity, Harvard School of Dental Medicine, Boston, Massachusetts.
Department of Periodontology, Faculty of Dentistry, University of Toronto, Toronto, Ontario, Canada; Matrix Dynamics Group, Faculty of Dentistry, University of Toronto, Toronto, Ontario, Canada.
Am J Pathol. 2016 Jun;186(6):1417-26. doi: 10.1016/j.ajpath.2016.01.013. Epub 2016 Apr 9.
The balance between reactive oxygen species and antioxidants plays an important role in periodontal health. We previously demonstrated that high reactive oxygen species production by oral polymorphonuclear neutrophils (oPMNs) in chronic periodontitis (CP) refractory to conventional therapy is associated with severe destruction of periodontium. Herein, we show that inhibition of antioxidant production through down-regulation of nuclear factor erythroid 2-related factor 2 (Nrf2) pathway in oPMN, despite enhanced recruitment in the oral cavity, is associated with severe CP. Twenty-four genes in the Nrf2-mediated oxidative stress response pathway were down-regulated in PMNs of diseased patients. Downstream of Nrf2, levels of oPMN superoxide dismutase 1 and catalase were decreased in severe CP, despite increased recruitment. Nrf2(-/-) mice had more severe loss of periodontium in response to periodontitis-inducing subgingival ligatures compared with wild-types. Levels of 8-hydroxy-deoxyguanosine were increased in periodontal lesions of Nrf2(-/-) mice, indicating high oxidative damage. We report, for the first time, Nrf2 pathway down-regulation in oPMNs of patients with severe CP. PMNs of CP patients may be primed for low antioxidant response in the context of high recruitment in the oral cavity, resulting in increased oxidative tissue damage.
活性氧与抗氧化剂之间的平衡在牙周健康中起着重要作用。我们之前证明,在对传统治疗难治的慢性牙周炎(CP)中,口腔多形核中性粒细胞(oPMN)产生的高活性氧与牙周组织的严重破坏有关。在此,我们表明,尽管oPMN在口腔中的募集增加,但通过下调核因子红细胞2相关因子2(Nrf2)途径抑制抗氧化剂的产生与严重的CP有关。在患病患者的PMN中,Nrf2介导的氧化应激反应途径中的24个基因被下调。在Nrf2的下游,尽管募集增加,但在严重CP中oPMN超氧化物歧化酶1和过氧化氢酶的水平降低。与野生型相比,Nrf2(-/-)小鼠在接受诱导牙周炎的龈下结扎后牙周组织丧失更严重。Nrf2(-/-)小鼠牙周病变中8-羟基脱氧鸟苷水平升高,表明氧化损伤严重。我们首次报道了严重CP患者oPMN中Nrf2途径下调。CP患者的PMN在口腔中募集增加的情况下可能会引发低抗氧化反应,从而导致氧化组织损伤增加。