A Reversible Fluorescent Probe for In Situ Monitoring Redox Imbalance during Mitophagy.
Junbin LiLifei SongWeiguo HuQin ZuoRoumei LiMin DaiYibo ZhouZhihe QingPublished in: Analytical chemistry (2023)
Mitophagy is the lysosome-dependent degradation of damaged and dysfunctional mitochondria, which is closely associated with H 2 O 2 -related redox imbalance and pathological processes. However, development of fast-responding and highly sensitive reversible fluorescent probes for monitoring of mitochondrial H 2 O 2 dynamics is still lacking. Herein, we report a reversible fluorescent probe ( M-HP ) that enables real-time imaging of H 2 O 2 -related redox imbalance. In vitro studies demonstrated that M-HP had a rapid response and high sensitivity to the H 2 O 2 /GSH redox cycle, with a detection limit of 17 nM for H 2 O 2 . M-HP was applied to imaging of H 2 O 2 fluctuation in living cells with excellent reversibility and mitochondrial targeting. M-HP reveals an increase in mitochondrial H 2 O 2 under lipopolysaccharide stimulation and a decrease in H 2 O 2 following the combined treatment with rapamycin. This suggests that the level of oxidative stress is significantly suppressed after the enhancement of mitophagy. The rationally designed M-HP offers a powerful tool for understanding redox imbalance during mitophagy.
Keyphrases
- living cells
- fluorescent probe
- oxidative stress
- high resolution
- nlrp inflammasome
- electron transfer
- single molecule
- loop mediated isothermal amplification
- induced apoptosis
- ischemia reperfusion injury
- inflammatory response
- small molecule
- dna damage
- cell death
- toll like receptor
- diabetic rats
- mass spectrometry
- combination therapy
- reactive oxygen species
- lps induced
- heat stress
- drug induced
- real time pcr