Department of Pediatric Surgery, University Medical Center Hamburg-Eppendorf (UKE), Hamburg, Germany.
Front Immunol. 2021 Jan 19;11:582895. doi: 10.3389/fimmu.2020.582895. eCollection 2020.
Neutrophil extracellular traps (NETs) are a defense mechanism in which neutrophils cast a net-like structure in response to microbial infection. NETs consist of decondensed chromatin and about 30 enzymes and peptides. Some components, such as neutrophil elastase (NE) and myeloperoxidase (MPO), present antimicrobial but also cytotoxic properties, leading to tissue injury. Many inflammatory diseases are associated with NETs, and their final role has not been identified. Pulmonary surfactant is known to have immunoregulatory abilities that alter the function of adaptive and innate immune cells. The aim of this study was to investigate the hypothesis that natural surfactant preparations inhibit the formation of NETs.
The effect of two natural surfactants (Alveofact and Curosurf) on spontaneous and phorbol-12-myristate-13-acetate-induced NET formation by neutrophils isolated by magnetic cell sorting from healthy individuals was examined. NETs were quantitatively detected by absorption and fluorometric-based assays for the NET-specific proteins (NE, MPO) and cell-free DNA. Immunofluorescence microscopy images were used for visualization.
Both surfactant preparations exerted a dose-dependent inhibitory effect on NET formation. Samples treated with higher concentrations and with 30 min pre-incubation prior to stimulation with phorbol-12-myristate-13-acetate had significantly lower levels of NET-specific proteins and cell-free DNA compared to untreated samples. Immunofluorescence microscopy confirmed these findings.
The described dose-dependent modulation of NET formation ex vivo suggests an interaction between exogenous surfactant supplementation and neutrophil granulocytes. The immunoregulatory effects of surfactant preparations should be considered for further examination of inflammatory diseases.
中性粒细胞胞外诱捕网(NETs)是一种防御机制,其中中性粒细胞在微生物感染时形成网状结构。NETs 由去凝聚的染色质和大约 30 种酶和肽组成。一些成分,如中性粒细胞弹性蛋白酶(NE)和髓过氧化物酶(MPO),具有抗菌但也具有细胞毒性的特性,导致组织损伤。许多炎症性疾病与 NETs 有关,但其最终作用尚未确定。肺表面活性剂已知具有免疫调节能力,可改变适应性和固有免疫细胞的功能。本研究旨在验证天然表面活性剂制剂是否能抑制 NETs 的形成。
通过磁细胞分选从健康个体中分离出的中性粒细胞,研究了两种天然表面活性剂(Alveofact 和 Curosurf)对自发和佛波醇-12-肉豆蔻酸-13-乙酸酯诱导的 NET 形成的影响。通过吸收和荧光基于 NET 特异性蛋白(NE、MPO)和无细胞 DNA 的测定来定量检测 NETs。使用免疫荧光显微镜图像进行可视化。
两种表面活性剂制剂均对 NET 形成表现出剂量依赖性抑制作用。用较高浓度的样品处理并在用佛波醇-12-肉豆蔻酸-13-乙酸酯刺激前预孵育 30 分钟的样品与未经处理的样品相比,NET 特异性蛋白和无细胞 DNA 的水平显著降低。免疫荧光显微镜证实了这些发现。
描述的 NET 形成的体外剂量依赖性调节表明外源性表面活性剂补充与中性粒细胞粒细胞之间存在相互作用。应考虑表面活性剂制剂的免疫调节作用,以进一步研究炎症性疾病。