Multiplexed profiling of single-cell secretion on a hierarchical loading microwell chip

被引:0
作者
Shao, Ning [1 ]
Zhou, Yufu [1 ,2 ]
Liu, Xuewu [1 ]
机构
[1] Houston Methodist Res Inst, Dept Nanomed, Houston, TX 77030 USA
[2] Cent South Univ, Xiangya Hosp 3, Changsha 410008, Peoples R China
关键词
Microfluidics; Cytokine secretion; Single-cell analysis; Multiplexed detection; TCR-T cell; T-CELLS; IMMUNE; ACTIVATION; SURFACE; HETEROGENEITY; STIMULATION; MODULATION; EXPRESSION; RESPONSES; PATHWAYS;
D O I
10.1016/j.bios.2025.117711
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Protein secretion is involved in many biological processes, such as cellular communication, embryonic development, tissue homeostasis, disease pathogenesis, and execution of immune functions. Highly multiplexed detection of single-cell secretion is greatly needed but has always been challenging. Herein, we present a hierarchical loading microwell chip (HL-Chip)-based method that efficiently aligns thousands of single cells with multiple antibody-coated microbeads for highly multiplexed detection of secreted proteins from single cells. We demonstrate the applications of this platform in profiling secretion of six cytokines from single T cells and macrophages after pan-and antigen-specific stimulation. The 6-plex cytokine profiling reveals an early but transient cytokine burst and polyfunctional heterogeneity in antigen peptide-stimulated T cell receptor-engineered T (TCR-T) cells. This simple and versatile technology could find its application in single-cell measurements in both biological discoveries and clinical diagnosis.
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页数:10
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