Department of Anaesthesiology, University Medical Centre Regensburg, Franz-Josef-Strauss-Allee 11, 93053 Regensburg, Germany.
Department of Dermatology, University Medical Centre Regensburg, Franz-Josef-Strauss-Allee 11, 93053 Regensburg, Germany.
Biomolecules. 2024 Sep 30;14(10):1242. doi: 10.3390/biom14101242.
The application of normo- and hyperbaric O is a common therapy option in various disease patterns. Thereby, the applied O affects the whole body, including the blood and its components. This study investigates influences of pressure and oxygen fraction on human blood plasma, nutrient media, and the functions of neutrophil granulocytes (PMNs). Neutrophil migration, reactive oxygen species (ROS) production, and NETosis were examined by live cell imaging. The treatment of various matrices (Roswell Park Memorial Institute 1640 medium, Dulbecco's Modified Eagle's Medium, HO, human plasma, and isolated PMNs) with hyperbaric oxygen (HBO) was performed. In addition, the expression of different neutrophil surface epitopes (CD11b, CD62L, CD66b) and the oxidative burst were investigated by flow cytometry (FACS). The application of cold atmospheric plasma (CAP) to normoxic and normobaric culture media served as a positive control. Soluble reaction products such as HO, reactive nitrogen species (RNS: NO and NO), and ROS-dependent dihydrorhodamine oxidation were quantified by fluoro- and colorimetric assay kits. Under normobaric normoxia, PMNs migrate slower and shorter in comparison with normobaric hyper- or hypoxic conditions and hyperbaric hyperoxia. The pressure component has less effect on the migration behavior of PMNs than the O concentration. Individual PMN cells produce prolonged ROS at normoxic conditions. PMNs showed increased expression of CD11b in normobaric normoxia, lower expression of CD62L in normobaric normoxia, and lower expression of CD66b after HBO and CAP treatment. Treatment with CAP increased the amount of ROS and RNS in common culture media. Hyperbaric and normobaric O influences neutrophil functionality and surface epitopes in a measurable way, which may have an impact on disorders with neutrophil involvement. In the context of hyperbaric experiments, especially high amounts of HO in RPMI after hyperbaric oxygen should be taken into account. Therefore, our data support a critical indication for the use of normobaric and hyperbaric oxygen and conscientious and careful handling of oxygen in everyday clinical practice.
常压常氧、高压氧在各种疾病模式下的应用都是常见的治疗选择。因此,应用的氧气会影响全身,包括血液及其成分。本研究调查了压力和氧气分压对人血浆、营养培养基和中性粒细胞(PMN)功能的影响。通过活细胞成像研究了中性粒细胞迁移、活性氧(ROS)产生和 NETosis。用高压氧(HBO)处理各种基质(罗威尔帕克纪念研究所 1640 培养基、杜尔贝科改良伊格尔培养基、HO、人血浆和分离的PMN)。此外,通过流式细胞术(FACS)研究了不同中性粒细胞表面表型(CD11b、CD62L、CD66b)和氧化爆发的表达。将冷常压等离子体(CAP)应用于常氧和常气压培养基作为阳性对照。通过荧光和比色测定试剂盒定量测定可溶反应产物,如 HO、活性氮物种(RNS:NO 和 NO)和 ROS 依赖性二氢罗丹明氧化。在常气压常氧下,PMN 的迁移速度比常气压高氧或低氧以及高压高氧慢且短。压力因素对PMN迁移行为的影响小于 O 浓度。在常氧条件下,单个PMN 细胞产生延长的 ROS。在常气压常氧条件下,PMN 表现出 CD11b 的表达增加,CD62L 的表达降低,HBO 和 CAP 处理后 CD66b 的表达降低。CAP 处理增加了普通培养基中 ROS 和 RNS 的量。高压和常氧以可测量的方式影响中性粒细胞的功能和表面表型,这可能对涉及中性粒细胞的疾病产生影响。在高压实验的背景下,特别是高压氧后 RPMI 中高浓度的 HO 应予以考虑。因此,我们的数据支持对常压和高压氧的使用进行谨慎的临床指征,并在日常临床实践中谨慎小心地处理氧气。