Mitochondrial
membrane potential (ΔΨm) is
a key indicator of cell health or injury due to its vital roles in
adenosine 5′-triphosphate synthesis. Thus, monitoring ΔΨm is of great significance for the assessment of cell status,
diagnosis of diseases, and medicament screening. Cationic fluorescent
probes suffer from severe photobleaching or false positive signals
due to the luminescence of the probe on non-mitochondria. Herein,
we report a lipophilic cationic fluorescent probe [1-methyl-2-(4-(1,2,2-triphenylvinyl)styryl)-β-naphthothiazol-1-ium
trifluoromethanesulfonate (TPE-NT)] with the features
of aggregation-induced emission and intramolecular charge transfer
for imaging ΔΨm in live cells. TPE-NT is enriched on the surface of the mitochondrial inner membrane due
to the negative ΔΨm, and its fluorescence is
activated in the high-viscosity microenvironment. The false positive
signals of emission from TPE-NT on non-mitochondria are
therefore effectively eliminated. Moreover, TPE-NT exhibits
a Stokes shift of >200 nm, near-infrared (∼675 nm) emission,
excellent photostability, and low cytotoxicity, which facilitate real-time
imaging in live cells. Cell imaging confirmed that the probe can rapidly
and reliably report mitochondrial depolarization (decrement of ΔΨm) during cell damage caused by CCCP and H2O2 as well as mitochondrial polarization (increment of ΔΨm) by oligomycin. Furthermore, the probe successfully detected
the reduction of ΔΨm in these cell models of
hypoxia, heat damage, acidification, aging, inflammation, mitophagy,
and apoptosis caused by hypoxia, heatstroke, lactate/pyruvate, doxorubicin,
lipopolysaccharide, rapamycin, monensin, and nystatin, respectively.