Intravital observation of high-scattering and dense-labeling hepatic tissues using multi-photon fluorescence microscopy.
Runze ChenShiyi PengQiming XiaTianxiang WuJunyan ZhengHaiyan QinJun QianPublished in: Journal of biophotonics (2024)
Achieving high-resolution and large-depth microscopic imaging in vivo under conditions characterized by high-scattering and dense-labeling, as commonly encountered in the liver, poses a formidable challenge. Here, through the optimization of multi-photon fluorescence excitation window, tailored to the unique optical properties of the liver, intravital microscopic imaging of hepatocytes and hepatic blood vessels with high spatial resolution was attained. It's worth noting that resolution degradation caused by tissue scattering of excitation light was mitigated by accounting for moderate tissue self-absorption. Leveraging high-quality multi-photon fluorescence microscopy, we discerned structural and functional alterations in hepatocytes during drug-induced acute liver failure. Furthermore, a reduction in indocyanine green metabolism rates associated with acute liver failure was observed using NIR-II fluorescence macroscopic imaging.
Keyphrases
- liver failure
- high resolution
- single molecule
- energy transfer
- living cells
- hepatitis b virus
- mass spectrometry
- monte carlo
- high speed
- optical coherence tomography
- liver injury
- gene expression
- tandem mass spectrometry
- emergency department
- high intensity
- intensive care unit
- extracorporeal membrane oxygenation
- drug delivery
- liquid chromatography