toll样受体2和4在根管病原体刺激下巨噬细胞产生活性氧和一氧化氮中的作用。

L G Marcato, A P Ferlini, R C F Bonfim, M L Ramos-Jorge, C Ropert, L F C Afonso, L Q Vieira, A P R Sobrinho
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引用次数: 40

摘要

根尖周病变是由于宿主对根管感染的免疫反应的激活和相互作用而产生的。最近发现的toll样受体(TLR)似乎参与了对无数微生物的免疫反应的识别和发展。然而,关于TLR在诱发根尖周围病变中的作用的信息很少。方法:研究TLR-2和TLR-4在核梭菌和厌氧菌胃链球菌刺激小鼠巨噬细胞活化中的作用。评估了一氧化氮(NO)和活性氧(ROS)的产生。结果:结果表明,TLR-2和TLR-4参与了活化巨噬细胞产生ROS的过程。无论是否添加干扰素- γ (ifn - γ),这些微生物诱导TLR-2胜任和TLR-2缺失的巨噬细胞产生相似水平的NO,排除了TLR-2在这些细菌诱导的NO产生中的作用。在不添加ifn - γ的情况下,只有厌氧p诱导tlr -4胜任的巨噬细胞产生NO。然而,加入ifn - γ后,核仁梭菌诱导巨噬细胞产生NO。因此,ifn - γ和这些微生物刺激的NO产生似乎与tlr -4无关。结论:TLR-2似乎参与了巨噬细胞对普遍存在的根管细菌产生ROS的诱导,而只有F. nucleatum诱导了tlr -4胜任的巨噬细胞产生ROS。两种微生物均显著诱导了大量不依赖于TLR-2和TLR-4的NO。我们得出结论,微生物可能通过激活巨噬细胞产生NO和ROS参与根尖周围病变的诱导和进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of Toll-like receptors 2 and 4 on reactive oxygen species and nitric oxide production by macrophage cells stimulated with root canal pathogens.

Introduction: Periapical lesions arise as a result of the activation and interaction of the host immune responses against root canal infection. Recently identified Toll-like receptors (TLR) seem to be involved in the recognition and development of immune responses against a myriad of microorganisms. However, very little information is available on the role of TLR in the induction of periapical lesions.

Method: The role of TLR-2 and TLR-4 in the activation of murine macrophages stimulated using Fusobacterium nucleatum and Peptostreptococcus anaerobius was investigated. The production of nitric oxide (NO) and reactive oxygen species (ROS) was assessed.

Results: The results demonstrate that TLR-2 and TLR-4 are involved in the production of ROS by activated macrophages. The microorganisms induced similar levels of NO production by TLR-2-competent and TLR-2-deficient macrophages, regardless of the addition of interferon-gamma (IFN-gamma), ruling out a role for TLR-2 in the NO production induced by these bacteria. Only P. anaerobius induced NO production by TLR-4-competent macrophages without the addition of IFN-gamma. However, after IFN-gamma addition, F. nucleatum induced macrophage NO production. Therefore, NO production stimulated by IFN-gamma and these microorganisms seems to be TLR-4-independent.

Conclusion: TLR-2 seems to be involved in the induction of ROS production by macrophages in response to prevalent root canal bacteria, while only F. nucleatum induced ROS production by TLR-4-competent macrophages. Both microorganisms significantly induced large amounts of NO independent of TLR-2 and TLR-4. We conclude that microorganisms may participate in the induction and progression of periapical lesions through NO and ROS production by activated macrophages.

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