William G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, OH, United States.
Laboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, United States.
Front Immunol. 2021 May 12;12:671546. doi: 10.3389/fimmu.2021.671546. eCollection 2021.
Neutrophils are known to be the first responders to infection or injury. However, as inflammation progresses, other leukocytes become increasingly important in inflammation propagation, tissue reconstruction, and inflammation resolution. In recent years, there has been an increase in publications that analyze neutrophil behavior , but there remains a gap in the literature for technologies that enable quantitatively measuring interactions between different types of human leukocytes. Here, we used an platform that mimics inflammation by inducing neutrophil swarming to analyze the behavior of various leukocytes in a swarming setting. Using human peripheral blood leukocytes isolated directly from whole blood, we found that myeloid cells and lymphoid cells had different migratory behaviors. Myeloid cells, which are predominately neutrophils, exhibited swarming behavior. This behavior was not seen with lymphoid cells. We perturbed the peripheral blood leukocyte system by adding exogenous leukotriene B (LTB) to the medium. Notably, only the myeloid cell compartment was significantly changed by the addition of LTB. Additionally, LTB had no significant impact on myeloid cell migration during the recruitment phase of swarming. To further investigate the myeloid cell compartment, we isolated neutrophils and monocytes to analyze their interaction on the platform. We found that neutrophils increase monocyte migration toward the bioparticle clusters, as measured through speed, chemotactic index, track straightness, and swarm size. These results were confirmed with mouse experiments, where monocyte accumulation only occurred when neutrophils were present. Additionally, we found that both neutrophils and monocytes release the monocyte chemoattractant proteins CCL2 and CCL3 in the presence of bioparticles. Furthermore, extracellular vesicles from swarming neutrophils caused monocyte activation. These findings suggest that neutrophils play an essential role in the onset of inflammation not only by sealing off the site of infection or injury, but also by recruiting additional leukocytes to the site.
中性粒细胞是已知的对感染或损伤的第一反应者。然而,随着炎症的进展,其他白细胞在炎症传播、组织重建和炎症消退中变得越来越重要。近年来,分析中性粒细胞行为的出版物有所增加,但在能够定量测量不同类型人白细胞之间相互作用的技术方面仍存在空白。在这里,我们使用一种通过诱导中性粒细胞群集来模拟炎症的平台,来分析各种白细胞在群集环境中的行为。使用直接从全血中分离的人外周血白细胞,我们发现髓样细胞和淋巴样细胞具有不同的迁移行为。髓样细胞,主要是中性粒细胞,表现出群集行为。淋巴样细胞则没有表现出这种行为。我们通过向培养基中添加外源性白三烯 B (LTB) 来干扰外周血白细胞系统。值得注意的是,只有髓样细胞区室因添加 LTB 而发生显著变化。此外,LTB 对群集募集阶段的髓样细胞迁移没有显著影响。为了进一步研究髓样细胞区室,我们分离了中性粒细胞和单核细胞,以在平台上分析它们的相互作用。我们发现,中性粒细胞增加单核细胞向生物颗粒簇的迁移,这可以通过速度、趋化指数、轨迹直线度和群集大小来衡量。这些结果在 小鼠实验中得到了证实,只有当存在中性粒细胞时才会发生单核细胞聚集。此外,我们发现,在存在生物颗粒的情况下,中性粒细胞和单核细胞都会释放单核细胞趋化蛋白 CCL2 和 CCL3。此外,来自群集中性粒细胞的细胞外囊泡引起单核细胞激活。这些发现表明,中性粒细胞不仅通过封锁感染或损伤部位,而且通过招募额外的白细胞到该部位,在炎症的发生中起着至关重要的作用。