Tracking Cell Viability for Adipose-Derived Mesenchymal Stem Cell-Based Therapy by Quantitative Fluorescence Imaging in the Second Near-Infrared Window.
Naishun LiaoLichao SuYanbing CaoLiman QiuRong XieFang PengZhixiong CaiXiao-Long LiuJibin SongYongyi ZengPublished in: ACS nano (2022)
Cell survival rate determines engraftment efficiency in adipose-derived mesenchymal stem cell (ADSC)-based regenerative medicine. In vivo monitoring of ADSC viability to achieve effective tissue regeneration is a major challenge for ADSC therapy. Here, we developed an activated near-infrared II (NIR-II) fluorescent nanoparticle consisting of lanthanide-based down-conversion nanoparticles (DCNPs) and IR786s (DCNP@IR786s) for cell labeling and real-time tracking of ADSC viability in vivo . In dying ADSCs due to excessive ROS generation, absorption competition-induced emission of IR786s was destroyed, which could turn on the NIR-II fluorescent intensity of DCNPs at 1550 nm by 808 nm laser excitation. In contrast, the NIR-II fluorescent intensity of DCNPs was stable at 1550 nm by 980 nm laser excitation. This ratiometric fluorescent signal was precise and sensitive for tracking ADSC viability in vivo . Significantly, the nanoparticle could be applied to quantitively evaluate stem cell viability in real-time in vivo . Using this method, we successfully sought two small molecules including glutathione and dexamethasone that could improve stem cell engraftment efficiency and enhance ADSC therapy in a liver fibrotic mouse model. Therefore, we provide a potential strategy for real-time in vivo quantitative tracking of stem cell viability in ADSC therapy.
Keyphrases
- photodynamic therapy
- fluorescence imaging
- living cells
- fluorescent probe
- stem cells
- quantum dots
- mesenchymal stem cells
- mouse model
- cell therapy
- energy transfer
- dna damage
- magnetic resonance imaging
- oxidative stress
- risk assessment
- physical activity
- high intensity
- nitric oxide
- cell death
- computed tomography
- body mass index
- diabetic rats
- high dose
- endothelial cells
- reactive oxygen species
- weight gain
- iron oxide