Aratani Yasuaki, Miura Noriko, Ohno Naohito, Suzuki Kazuo
Graduate School of Nanobioscience, Yokohama City University.
Med Mycol J. 2012;53(2):123-8. doi: 10.3314/mmj.53.123.
Neutrophil accumulation is a critical event in the pathogenesis of inflammation. The generation of hypochlorous acid by myeloperoxidase (MPO) in neutrophils is crucial to the host defense response. MPO-deficient (MPO-KO) mice showed severely reduced cytotoxicity to Candida albicans, Aspergillus fumigatus, Cryptococcus neoformans and other microorganisms, demonstrating that an MPO-dependent oxidative system is important for in vivo host defense against fungi. On the other hand, impaired reactive oxygen species (ROS) production by neutrophils has previously been shown to cause an abnormal inflammatory response. In the present study, we have found that MPO-KO mice exhibit more severe pulmonary inflammation than wild-type mice when challenged with an intranasal administration of zymosan. In addition to measuring the kinetics of neutrophil accumulation, we also measured the production of macrophage inflammatory protein-2 (MIP-2) in the lung, and we correlate the degree of neutrophil accumulation with the production of this mediator. Our results demonstrate that MPO regulates the production of MIP-2, which may modulate neutrophil accumulation during lung inflammation.
中性粒细胞聚集是炎症发病机制中的关键事件。中性粒细胞中的髓过氧化物酶(MPO)产生次氯酸对宿主防御反应至关重要。MPO缺陷(MPO-KO)小鼠对白色念珠菌、烟曲霉、新型隐球菌和其他微生物的细胞毒性严重降低,表明MPO依赖的氧化系统对体内宿主抗真菌防御很重要。另一方面,先前已表明中性粒细胞产生活性氧(ROS)受损会导致异常炎症反应。在本研究中,我们发现当经鼻给予酵母聚糖刺激时,MPO-KO小鼠比野生型小鼠表现出更严重的肺部炎症。除了测量中性粒细胞聚集的动力学外,我们还测量了肺中巨噬细胞炎性蛋白-2(MIP-2)的产生,并将中性粒细胞聚集程度与该介质的产生相关联。我们的结果表明,MPO调节MIP-2的产生,这可能在肺部炎症期间调节中性粒细胞聚集。