Simultaneous two-photon intravital imaging of viscosity and superoxide radical anion by a styrylpyridinium-based fluorescent probe

被引:9
|
作者
Wang, Si-Yuan [1 ]
Liu, Jun-Ru [2 ]
Ju, Zheng-Hua [3 ]
Tian, Di-Hua [1 ]
Chai, Zuo-Hu [1 ]
Zhang, Yu [1 ]
Dai, Fang [1 ]
Zhang, Shengxiang [2 ]
Zhou, Bo [1 ]
机构
[1] Lanzhou Univ, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
[2] Lanzhou Univ, Sch Life Sci, Gansu Key Lab Biomonitoring & Bioremediat Environm, Lanzhou 730000, Peoples R China
[3] Lanzhou Univ, Ctr Anal & Testing, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金;
关键词
Fluorescent probe; Dual; -function; Viscosity; Superoxide radical anion; Intravital; imaging; Two; -photon; MITOCHONDRIA; CELLS; ROTOR;
D O I
10.1016/j.snb.2023.133470
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Simultaneous sensing of cellular microenvironment parameters and redox signaling molecules by a single fluorescent probe allows an efficient access to numerous applications ranging from convenient diagnostic assays to investigation on their pathophysiological roles and cross-link. Focusing on a lack of efficient molecule tools for simultaneous intravital imaging of mitochondrial viscosity and superoxide radical anion (O2 center dot-), we bridged diethylaminobenzene with diphenylphosphinate-modified pyridinium moiety by an olefinic bond to construct a styrylpyridinium-based two-photon fluorescent probe V-OS. V-OS triggered a turn-on response either at 625 nm to viscosity which blocks intramolecular rotation, or at 530 nm to O2 center dot- via nucleophilic attack of O2 center dot- followed by 1,6-elimination. With the aid of the two-photon probe, we not only identified the cross-talk between viscosity and O2 center dot- but successfully mapped the burst of O2 center dot- and the increased viscosity during either cellular ferroptosis process or cerebral ischemia reperfusion injury of living mice.
引用
收藏
页数:9
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