Prolo Carolina, Alvarez María Noel, Radi Rafael
Center for Free Radical and Biomedical Research, Departamento de Bioquímica, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.
Biofactors. 2014 Mar-Apr;40(2):215-25. doi: 10.1002/biof.1150. Epub 2013 Nov 26.
Macrophages are among the first cellular actors facing the invasion of microorganisms. These cells are able to internalize pathogens and destroy them by means of toxic mediators, many of which are produced enzymatically and have strong oxidizing capacity. Indeed, macrophages count on the NADPH oxidase complex activity, which is triggered during pathogen invasion and leads to the production of superoxide radical inside the phagosome. At the same time, the induction of nitric oxide synthase results in the production of nitric oxide in the cytosol which is able to readily diffuse to the phagocytic vacuole. Superoxide radical and nitric oxide react at diffusion controlled rates with each other inside the phagosome to yield peroxynitrite, a powerful oxidant capable to kill micro-organisms. Peroxynitrite toxicity resides on oxidations and nitrations of biomolecules in the target cell. The central role of peroxynitrite as a key effector molecule in the control of infections has been proven in a wide number of models. However, some microorganisms and virulent strains adapt to survive inside the potentially hostile oxidizing microenvironment of the phagosome by either impeding peroxynitrite formation or rapidly detoxifying it once formed. In this context, the outcome of the infection process is a result of the interplay between the macrophage-derived oxidizing cytotoxins such as peroxynitrite and the antioxidant defense machinery of the invading pathogens.
巨噬细胞是最早面对微生物入侵的细胞参与者之一。这些细胞能够内化病原体并通过毒性介质将其摧毁,其中许多毒性介质是通过酶促产生的,具有很强的氧化能力。实际上,巨噬细胞依赖于NADPH氧化酶复合体的活性,该活性在病原体入侵时被触发,并导致吞噬体内产生超氧自由基。与此同时,一氧化氮合酶的诱导导致细胞质中产生一氧化氮,一氧化氮能够迅速扩散到吞噬泡中。超氧自由基和一氧化氮在吞噬体内以扩散控制的速率相互反应,生成过氧亚硝酸盐,一种能够杀死微生物的强大氧化剂。过氧亚硝酸盐的毒性在于对靶细胞中生物分子的氧化和硝化作用。在大量模型中已证明过氧亚硝酸盐作为控制感染的关键效应分子的核心作用。然而,一些微生物和毒力菌株通过阻碍过氧亚硝酸盐的形成或一旦形成就迅速将其解毒,从而适应在吞噬体潜在的敌对氧化微环境中生存。在这种情况下,感染过程的结果是巨噬细胞衍生的氧化细胞毒素(如过氧亚硝酸盐)与入侵病原体的抗氧化防御机制之间相互作用的结果。