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局部趋化因子麻痹,牙龈卟啉单胞菌的一种新型致病机制。

Local chemokine paralysis, a novel pathogenic mechanism for Porphyromonas gingivalis.

作者信息

Darveau R P, Belton C M, Reife R A, Lamont R J

机构信息

Bristol-Myers Squibb Pharmaceutical Research Institute, Seattle, Washington 98121, USA.

出版信息

Infect Immun. 1998 Apr;66(4):1660-5. doi: 10.1128/IAI.66.4.1660-1665.1998.

Abstract

Periodontitis, which is widespread in the adult population, is a persistent bacterial infection associated with Porphyromonas gingivalis. Gingival epithelial cells are among the first cells encountered by both P. gingivalis and commensal oral bacteria. The chemokine interleukin 8 (IL-8), a potent chemoattractant and activator of polymorphonuclear leukocytes, was secreted by gingival epithelial cells in response to components of the normal oral flora. In contrast, P. gingivalis was found to strongly inhibit IL-8 accumulation from gingival epithelial cells. Inhibition was associated with a decrease in mRNA for IL-8. Antagonism of IL-8 accumulation did not occur in KB cells, an epithelial cell line that does not support high levels of intracellular invasion by P. gingivalis. Furthermore, a noninvasive mutant of P. gingivalis was unable to antagonize IL-8 accumulation. Invasion-dependent destruction of the gingival IL-8 chemokine gradient at sites of P. gingivalis colonization (local chemokine paralysis) will severely impair mucosal defense and represents a novel mechanism for bacterial colonization of host tissue.

摘要

牙周炎在成年人群中广泛存在,是一种与牙龈卟啉单胞菌相关的持续性细菌感染。牙龈上皮细胞是牙龈卟啉单胞菌和口腔共生菌最先接触的细胞之一。趋化因子白细胞介素8(IL-8)是一种有效的多形核白细胞趋化剂和激活剂,牙龈上皮细胞会对正常口腔菌群的成分作出反应而分泌IL-8。相比之下,发现牙龈卟啉单胞菌能强烈抑制牙龈上皮细胞中IL-8的积累。这种抑制与IL-8的mRNA减少有关。在KB细胞(一种不支持牙龈卟啉单胞菌高水平细胞内侵袭的上皮细胞系)中未出现IL-8积累的拮抗作用。此外,牙龈卟啉单胞菌的非侵袭性突变体无法拮抗IL-8的积累。在牙龈卟啉单胞菌定植部位,依赖侵袭的牙龈IL-8趋化因子梯度破坏(局部趋化因子麻痹)将严重损害黏膜防御,并代表宿主组织细菌定植的一种新机制。

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