Detection of LPS‐induced macrophage activation with single‐cell resolution through DC insulator‐based electrokinetic devices

Abstract

Macrophages are considered critical in the initiation, maintenance, and resolution of inflammation. Lipopolysaccharide (LPS)‐induced inflammation is often used as a model to understand the cell inflammation responses. Current techniques identifying the LPS‐induced inflammation are experiencing cell destruction or cell labeling or are based on the whole cell population information with low identification degree. This limits the detection process with time‐consuming cytokine selection, low resolution of population heterogeneity, and unavailability for their next use. Direct current insulator‐based electrokinetics (DC‐iEK) is introduced to achieve an easier and noninvasive identification of inflamed cells with high resolution. A biophysical scale is also established first time for screening medicine in the treatment of inflammation. The new microfluidic design concentrates cells with applied voltages forming streamline providing more stable cell capture conditions and unique biophysical factors at different capture positions. The average electric field of the cell capture positions is recorded to characterize each cell population. The characterization value of macrophage decreases from to 1.61 × 104 V/m when treated with 0.1 mM LPS and to 1.42 × 104 V/m when treated with 1 mM LPS. By treating the inflamed macrophages with representative effective medicines, healing signals could also be detected by a newly established inflammation scale. The cells showed proliferation and functional activity after extraction. DC‐iEK has provided an easy and noninvasive approach to identify inflammation for further fundamental and clinical precision medicine use.