Hepatic ischemia-reperfusion injury (HIRI) is a relatively common complication of liver resection and transplantation that is intimately connected to oxidative stress. The superoxide anion radical (O 2 •- ), as the first reactive oxygen species produced by organisms, is an important marker of HIRI. The endoplasmic reticulum (ER) is an essential site for O 2 •- production, especially ER oxidative stress, which is closely linked to HIRI. Thus, dynamic variations in ER O 2 •- may accurately indicate the HIRI extent. However, there is still a lack of tools for the dynamic reversible detection of ER O 2 •- . Therefore, we designed and prepared an ER-targeted fluorescent reversible probe DPC for real-time tracing of O 2 •- fluctuations. We successfully observed a marked increase in ER O 2 •- levels in HIRI mice. A potential NADPH oxidase 4-ER O 2 •- -SERCA2b-caspase 4 signaling pathway in HIRI mice was also revealed. Attractively, DPC was successfully used for precise fluorescent navigation and excision of HIRI sites.
Keyphrases
- endoplasmic reticulum
- ischemia reperfusion injury
- oxidative stress
- fluorescence imaging
- signaling pathway
- reactive oxygen species
- induced apoptosis
- quantum dots
- photodynamic therapy
- living cells
- bone marrow
- drug delivery
- cell death
- nitric oxide
- multidrug resistant
- mesenchymal stem cells
- fluorescent probe
- loop mediated isothermal amplification