Björnsdottir Halla, Dahlstrand Rudin Agnes, Klose Felix P, Elmwall Jonas, Welin Amanda, Stylianou Marios, Christenson Karin, Urban Constantin F, Forsman Huamei, Dahlgren Claes, Karlsson Anna, Bylund Johan
Department of Oral Microbiology and Immunology, Institute of Odontology, Sahlgrenska Academy at University of Gothenburg , Gothenburg , Sweden.
The Phagocyte Research Laboratory, Department of Rheumatology and Inflammation Research, Institute of Medicine, Sahlgrenska Academy at University of Gothenburg , Gothenburg , Sweden.
Front Immunol. 2017 Mar 9;8:257. doi: 10.3389/fimmu.2017.00257. eCollection 2017.
Neutrophils have the ability to capture and kill microbes extracellularly through the formation of neutrophil extracellular traps (NETs). These are DNA and protein structures that neutrophils release extracellularly and are believed to function as a defense mechanism against microbes. The classic NET formation process, triggered by, e.g., bacteria, fungi, or by direct stimulation of protein kinase C through phorbol myristate acetate, is an active process that takes several hours and relies on the production of reactive oxygen species (ROS) that are further modified by myeloperoxidase (MPO). We show here that NET-like structures can also be formed by neutrophils after interaction with phenol-soluble modulin α (PSMα) that are cytotoxic membrane-disturbing peptides, secreted from community-acquired methicillin-resistant (CA-MRSA). The PSMα-induced NETs contained the typical protein markers and were able to capture microbes. The PSMα-induced NET structures were disintegrated upon prolonged exposure to DNase-positive but not on exposure to DNase-negative . Opposed to classic NETosis, PSMα-triggered NET formation occurred very rapidly, independently of ROS or MPO, and was also manifest at 4°C. These data indicate that rapid NETs release may result from cytotoxic membrane disturbance by PSMα peptides, a process that may be of importance for CA-MRSA virulence.
中性粒细胞能够通过形成中性粒细胞胞外诱捕网(NETs)在细胞外捕获并杀死微生物。这些是中性粒细胞释放到细胞外的DNA和蛋白质结构,被认为是一种抵御微生物的防御机制。经典的NET形成过程,例如由细菌、真菌触发,或通过佛波酯肉豆蔻酸乙酸酯直接刺激蛋白激酶C引发,是一个耗时数小时的活跃过程,依赖于活性氧(ROS)的产生,而ROS会被髓过氧化物酶(MPO)进一步修饰。我们在此表明,中性粒细胞在与酚溶性调节素α(PSMα)相互作用后也能形成类NET结构,PSMα是社区获得性耐甲氧西林金黄色葡萄球菌(CA-MRSA)分泌的具有细胞毒性的膜干扰肽。PSMα诱导的NETs含有典型的蛋白质标志物,并且能够捕获微生物。PSMα诱导的NET结构在长时间暴露于DNA酶阳性环境中会解体,但暴露于DNA酶阴性环境中则不会。与经典的NETosis不同,PSMα触发的NET形成非常迅速,不依赖于ROS或MPO,并且在4°C时也会出现。这些数据表明,快速释放NETs可能是由PSMα肽引起的细胞毒性膜干扰导致的,这一过程可能对CA-MRSA的毒力具有重要意义。