A hemicyanine-based near-infrared fluorescent probe with large Stokes shift for non-invasive bioimaging of brown adipose tissue.
Ke XiangJinbing PanJiaojiao YuLehui XiaoShao-Kai SunRan ChengPublished in: Analytical methods : advancing methods and applications (2024)
Brown adipose tissue (BAT), characterized by the presence of numerous mitochondria, plays a key role in metabolism and energy expenditure. Accurately reporting the presence and activation of BAT is beneficial to study obesity, diabetes, and other metabolic disorders. Near-infrared (NIR) fluorescence imaging has the advantages of high sensitivity, non-radioactivity, and simple operation. However, most NIR probes for BAT imaging exhibit small Stokes shifts, which may lead to self-quenching, reducing the signal-to-noise ratio, and introducing cross-talk. Herein, we rationally designed and synthesized a series of hemicyanine-based NIR fluorescent probes HCYBAT-1-3. Among them, HCYBAT-1 demonstrated favorable properties such as near-infrared emission (776 nm), large Stokes shift (139 nm), good biocompatibility and specific mitochondrial targeting (Pearson's colocalization coefficient of 0.87). Meanwhile, HCYBAT-1 was successfully employed to differentiate BAT from white adipose tissue (WAT). Quantitative analysis of NIR fluorescent images showed that HCYBAT-1 could be used for real-time monitoring of BAT activation in mice stimulated by norepinephrine (NE) and cold exposure. Overall, probe HCYBAT-1 showcased its efficacy in non-invasive evaluation of BAT metabolism in vivo with high selectivity and sensitivity.
Keyphrases
- fluorescent probe
- living cells
- adipose tissue
- fluorescence imaging
- insulin resistance
- photodynamic therapy
- high fat diet
- type diabetes
- high fat diet induced
- metabolic syndrome
- cardiovascular disease
- oxidative stress
- weight loss
- deep learning
- air pollution
- small molecule
- skeletal muscle
- quantum dots
- physical activity
- reactive oxygen species
- drug delivery
- mass spectrometry
- diffusion weighted imaging
- endoplasmic reticulum