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Super-resolution imaging lysosome vesicles and establishing a gallbladder-visualizable zebrafish model via a fluorescence probe.
Guo, Chengxi; Wu, Yufang; Wang, Qiling; Li, Xiaoqi; Deng, Tao; Xia, Xiaotong; Li, Lei; Li, Huan; Lin, Chaozhan; Zhu, Chenchen; Liu, Fang.
Affiliation
  • Guo C; School of Pharmaceutical Sciences, Artemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
  • Wu Y; School of Pharmaceutical Sciences, Artemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
  • Wang Q; School of Pharmaceutical Sciences, Artemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
  • Li X; School of Pharmaceutical Sciences, Artemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
  • Deng T; School of Medicine, Foshan University, Foshan, 528000, China.
  • Xia X; School of Pharmaceutical Sciences, Artemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
  • Li L; School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430000, China. Electronic address: leileilesure@163.com.
  • Li H; Lingnan Medical Research Center, The First Affiliated Hospital, Guangzhou University of Chinese Medicine, Guangzhou, 510407, China.
  • Lin C; School of Pharmaceutical Sciences, Artemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
  • Zhu C; School of Pharmaceutical Sciences, Artemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China. Electronic address: zhucc@gzucm.edu.cn.
  • Liu F; School of Pharmaceutical Sciences, Artemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China. Electronic address: fangliu@gzucm.edu.cn.
Talanta ; 279: 126656, 2024 Nov 01.
Article de En | MEDLINE | ID: mdl-39098243
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.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Danio zébré / Colorants fluorescents / Vésicule biliaire / Lysosomes Limites: Animals / Humans Langue: En Journal: Talanta Année: 2024 Type de document: Article Pays d'affiliation: Chine Pays de publication: Pays-Bas

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Danio zébré / Colorants fluorescents / Vésicule biliaire / Lysosomes Limites: Animals / Humans Langue: En Journal: Talanta Année: 2024 Type de document: Article Pays d'affiliation: Chine Pays de publication: Pays-Bas