High-content and high-throughput identification of macrophage polarization phenotypes

被引:27
|
作者
Geng, Yingying [1 ,2 ]
Hardie, Joseph [2 ]
Landis, Ryan F. [2 ]
Mas-Rosario, Javier A. [1 ,2 ]
Chattopadhyay, Aritra Nath [2 ]
Keshri, Puspam [2 ]
Sun, Jiadi [2 ,3 ]
Rizzo, Erik M. [2 ]
Gopalakrishnan, Sanjana [2 ]
Farkas, Michelle E. [1 ,2 ]
Rotello, Vincent M. [1 ,2 ]
机构
[1] Univ Massachusetts, Mol & Cellular Biol Program, 710 N Pleasant St, Amherst, MA 01003 USA
[2] Univ Massachusetts, Dept Chem, 710 N Pleasant St, Amherst, MA 01003 USA
[3] Jiangnan Univ, Sch Food Sci, State Key Lab Food Sci & Technol, Wuxi, Jiangsu, Peoples R China
基金
美国国家卫生研究院;
关键词
TUMOR-ASSOCIATED MACROPHAGES; RAPID IDENTIFICATION; CELLS; ACTIVATION; CANCER; BACTERIA; MODULATION; MECHANISMS; PLASTICITY; MONOCYTES;
D O I
10.1039/d0sc02792h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Macrophages are plastic cells of the innate immune system that perform a wide range of immune- and homeostasis-related functions. Due to their plasticity, macrophages can polarize into a spectrum of activated phenotypes. Rapid identification of macrophage polarization states provides valuable information for drug discovery, toxicological screening, and immunotherapy evaluation. The complexity associated with macrophage activation limits the ability of current biomarker-based methods to rapidly identify unique activation states. In this study, we demonstrate the ability of a 2-element sensor array that provides an information-rich 5-channel output to successfully determine macrophage polarization phenotypes in a matter of minutes. The simple and robust sensor generates a high dimensional data array which enables accurate macrophage evaluations in standard cell lines and primary cells after cytokine treatment, as well as following exposure to a model disease environment.
引用
收藏
页码:8231 / 8239
页数:9
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