巨噬细胞
炎症
细胞生物学
体内
免疫系统
过剩1
门控
关节炎
类风湿性关节炎
化学
生物
免疫学
体外
神经科学
生物化学
遗传学
内分泌学
胰岛素
葡萄糖转运蛋白
作者
Heewon Cho,Haw‐Young Kwon,Amit Sharma,Sun Hyeok Lee,Xiao Liu,Naoki Miyamoto,Jong-Jin Kim,Sin‐Hyeog Im,Nam‐Young Kang,Young‐Tae Chang
标识
DOI:10.1038/s41467-022-33526-z
摘要
Abstract Macrophages play crucial roles in protecting our bodies from infection and cancers. As macrophages are multi-functional immune cells, they have diverse plastic subsets, such as M1 and M2, derived from naïve M0 cells. Subset-specific macrophage probes are essential for deciphering and monitoring the various activation of macrophages, but developing such probes has been challenging. Here we report a fluorescent probe, CDr17, which is selective for M1 macrophages over M2 or M0. The selective staining mechanism of CDr17 is explicated as Gating-Oriented Live-cell Distinction (GOLD) through overexpressed GLUT1 in M1 macrophages. Finally, we demonstrate the suitability of CDr17 to track M1 macrophages in vivo in a rheumatoid arthritis animal model.
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