转身(生物化学)
小胶质细胞
荧光
基质(水族馆)
化学
生物物理学
生物
生物化学
物理
光学
生态学
免疫学
炎症
作者
Beomsue Kim,Masahiro Fukuda,Jungyeol Lee,Dongdong Su,Srikanta Sanu,Aymeric Silvin,Audrey Tze Ting Khoo,Taejoon Kwon,Xiao Liu,Weijie Chi,Xiaogang Liu,Sejong Choi,Diana S. Y. Wan,Sung Jin Park,Jin‐Soo Kim,Florent Ginhoux,H. Shawn Je,Young‐Tae Chang
标识
DOI:10.1002/anie.201903058
摘要
Microglia, the brain-resident macrophage, are involved in brain development and contribute to the progression of neural disorders. Despite the importance of microglia, imaging of live microglia at a cellular resolution has been limited to transgenic mice. Efforts have therefore been dedicated to developing new methods for microglia detection and imaging. Using a thorough structure-activity relationships study, we developed CDr20, a high-performance fluorogenic chemical probe that enables the visualization of microglia both in vitro and in vivo. Using a genome-scale CRISPR-Cas9 knockout screen, the UDP-glucuronosyltransferase Ugt1a7c was identified as the target of CDr20. The glucuronidation of CDr20 by Ugt1a7c in microglia produces fluorescence.
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