BioMEMS Resource Center, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Shriners Burns Hospital, Boston, MA 02129, USA.
Lab Chip. 2019 Mar 27;19(7):1205-1216. doi: 10.1039/c8lc01263f.
Measurements of neutrophil activities such as cell migration and phagocytosis are generally performed using low-content bulk assays, which provide little detail activity at the single cell level, or flow cytometry methods, which have the single cell resolution but lack perspective on the kinetics of the process. Here, we present a microfluidic assay for measuring the essential functions that contribute to the antimicrobial activity of neutrophils: migration towards the target, and killing of microbes. The assay interrogates the interactions between isolated human neutrophils and populations of live, proliferating microbes. The outcome is measured in a binary mode that is reflective of in vivo infections, which are either cleared or endure the host response. The outcome of the interactions is also characterized at single cell resolution for both the neutrophils and the microbes. We applied the assay to test the response of neutrophils from intensive care patients to live Staphylococcus aureus, and observed alterations of antimicrobial neutrophil activity in patients, including those with sepsis. By directly measuring neutrophil activity against live targets at high spatial and temporal resolution, this assay provides unique insights into the life-or-death contest shaping the outcome of interactions between populations of neutrophils and microbes.
中性粒细胞活性的测量,如细胞迁移和吞噬作用,通常使用低含量的大容量分析进行,这些分析方法在单细胞水平上提供的细节活动很少,或者使用流式细胞术方法,这些方法具有单细胞分辨率,但缺乏对过程动力学的了解。在这里,我们提出了一种用于测量有助于中性粒细胞抗菌活性的基本功能的微流控分析:向靶细胞迁移和杀死微生物。该分析检测了分离的人中性粒细胞与活的、增殖的微生物群体之间的相互作用。结果以反映体内感染的二进制模式进行测量,感染要么被清除,要么经受住宿主反应。还以单细胞分辨率对中性粒细胞和微生物的相互作用结果进行了特征描述。我们应用该分析来测试重症监护病房患者的中性粒细胞对活的金黄色葡萄球菌的反应,并观察到感染患者(包括败血症患者)中性粒细胞抗菌活性的改变。通过直接以高时空分辨率测量针对活靶标的中性粒细胞活性,该分析提供了对塑造中性粒细胞和微生物群体之间相互作用结果的生死竞赛的独特见解。