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Updated: Jun 18, 2025

Imaging Subcellular Structures in the Living Zebrafish Embryo
Published on: April 2, 2016
Super-resolution imaging lysosome vesicles and establishing a gallbladder-visualizable zebrafish model via a
Chengxi Guo1, Yufang Wu1, Qiling Wang1
1School of Pharmaceutical Sciences, Artemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
Abstract:
Advanced probes for imaging viscous lipids microenvironment in vitro and in vivo are desirable for the study of membranous organelles and lipids traffic. Herein, a reaction-based dihydroquinoline probe (DCQ) was prepared via linking a diethylamino coumarin fluorophore with a N-methylquinoline moiety. DCQ is stable in low viscous aqueous mediums and exhibits green fluorescence, which undergoes fast autoxidation in high viscous mediums to form a fluorescent product with deep-red to near-infrared (NIR) emission, rendering the ability for dual-color imaging. Living cell imaging indicated that DCQ can effectively stain lysosomal membranes with deep-red fluorescence. Super-resolution imaging of lysosome vesicles has been achieved by DCQ and stimulated emission depletion (STED) microscopy. In addition, DCQ realizes multiple organs imaging in zebrafish, whose dual-color emission can perfectly discriminate zebrafish's yolk sac, digestive tract and gallbladder. Most importantly, DCQ has been successfully used to establish a gallbladder-visualizable zebrafish model for the evaluation of drug stress.

