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具核梭杆菌这种口腔细菌可诱导外周血单核细胞和多形核细胞发生凋亡性细胞死亡。

Induction of apoptotic cell death in peripheral blood mononuclear and polymorphonuclear cells by an oral bacterium, Fusobacterium nucleatum.

作者信息

Jewett A, Hume W R, Le H, Huynh T N, Han Y W, Cheng G, Shi W

机构信息

Department of Oral Biology and Oral Medicine, Dental Research Institute, University of California, Los Angeles, California 90095, USA.

出版信息

Infect Immun. 2000 Apr;68(4):1893-8. doi: 10.1128/IAI.68.4.1893-1898.2000.

Abstract

It is largely unknown why a variety of bacteria present in the oral cavity are capable of establishing themselves in the periodontal pockets of nonimmunocompromised individuals in the presence of competent immune effector cells. In this paper we present evidence for the immunosuppressive role of Fusobacterium nucleatum, a gram-negative oral bacterium which plays an important role in the generation of periodontal disease. Our studies indicate that the immunosuppressive role of F. nucleatum is largely due to the ability of this organism to induce apoptotic cell death in peripheral blood mononuclear cells (PBMCs) and in polymorphonuclear cells (PMNs). F. nucleatum treatment induced apoptosis of PBMCs and PMNs as assessed by an increase in subdiploid DNA content determined by DNA fragmentation and terminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end-labeling assays. The ability of F. nucleatum to induce apoptosis was abolished by either heat treatment or proteinase digestion but was retained after formaldehyde treatment, suggesting that a heat-labile surface protein component is responsible for bacterium-mediated cell apoptosis. The data also indicated that F. nucleatum-induced cell apoptosis requires activation of caspases and is protected by NF-kappaB. Possible mechanisms of F. nucleatum's role in the pathogenesis of periodontal disease are discussed.

摘要

目前尚不清楚为何口腔中存在的多种细菌能够在免疫功能正常的个体的牙周袋中,在有功能正常的免疫效应细胞存在的情况下定植。在本文中,我们提供了具核梭杆菌免疫抑制作用的证据,具核梭杆菌是一种革兰氏阴性口腔细菌,在牙周病的发生中起重要作用。我们的研究表明,具核梭杆菌的免疫抑制作用很大程度上归因于该菌诱导外周血单核细胞(PBMC)和多形核细胞(PMN)凋亡性细胞死亡的能力。通过DNA片段化和末端脱氧核苷酸转移酶介导的dUTP-生物素缺口末端标记试验测定的亚二倍体DNA含量增加来评估,具核梭杆菌处理可诱导PBMC和PMN凋亡。具核梭杆菌诱导凋亡的能力通过热处理或蛋白酶消化而被消除,但在甲醛处理后仍保留,这表明一种热不稳定的表面蛋白成分负责细菌介导的细胞凋亡。数据还表明,具核梭杆菌诱导的细胞凋亡需要半胱天冬酶的激活,并受到核因子κB的保护。讨论了具核梭杆菌在牙周病发病机制中的可能作用机制。

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