Xiao Xian, Wang Chenyu, Guo Xun, Xi Fengxue, Qian Qiuling, Liang Guoteng, Chen Ming, Sun Xiaoting, Szabo Balint, Jing Miao, Piatkevich Kiryl D
School of Life Sciences, Westlake University, Hangzhou, China.
Westlake Laboratory of Life Sciences and Biomedicine, Hangzhou, China.
Nat Methods. 2025 Jul 15. doi: 10.1038/s41592-025-02742-y.
Chemokines regulate immune cell migration in development, homeostasis and inflammation, but the precise spatiotemporal pattern of chemokine release in vivo remains elusive due to the constraints of existing detection methodologies. Here, we report the engineering and characterization of a genetically encoded green fluorescent chemokine sensor, named CRAFi-CCR2, which utilizes the CCR2 receptor as a sensing moiety. In astrocytes, hCRAFi-CCR2, derived from the human CCR2B receptor, exhibited ~300% increase in fluorescence in response to mCCL2, with nanomolar affinity (2.5 nM). Activation of hCRAFi-CCR2 did not affect downstream signaling pathways, such as calcium mobilization and receptor internalization. Using this sensor, we performed 17-20 h of real-time imaging to observe endogenous mCCL2 release under inflammatory conditions, both in cell culture and in mice. In mouse brain, we observed spatial heterogeneity of CCL2 signal response on a scale of about 20-50 µm, highlighting the complexity of the immune system's spatiotemporal signaling.
趋化因子在发育、体内平衡和炎症过程中调节免疫细胞迁移,但由于现有检测方法的限制,趋化因子在体内释放的精确时空模式仍不清楚。在此,我们报告了一种名为CRAFi-CCR2的基因编码绿色荧光趋化因子传感器的构建与表征,该传感器利用CCR2受体作为传感部分。在星形胶质细胞中,源自人CCR2B受体的hCRAFi-CCR2对mCCL2的荧光响应增加了约300%,具有纳摩尔亲和力(2.5 nM)。hCRAFi-CCR2的激活不影响下游信号通路,如钙动员和受体内化。使用该传感器,我们进行了17-20小时的实时成像,以观察细胞培养和小鼠炎症条件下内源性mCCL2的释放。在小鼠大脑中,我们观察到CCL2信号响应在约20-50μm尺度上的空间异质性,突出了免疫系统时空信号的复杂性。