Discrimination of lipid composition and cellular localization in human liver tissues by stimulated Raman scattering microscopy

J Biomed Opt. 2024 Jan;29(1):016008. doi: 10.1117/1.JBO.29.1.016008. Epub 2024 Jan 24.

Abstract

Significance: The molecular mechanisms driving the progression from nonalcoholic fatty liver (NAFL) to fibrosing steatohepatitis (NASH) are insufficiently understood. Techniques enabling the characterization of different lipid species with both chemical and spatial information can provide valuable insights into their contributions to the disease progression.

Aim: We extend the utility of stimulated Raman scattering (SRS) microscopy to characterize and quantify lipid species in liver tissue sections from patients with NAFL and NASH.

Approach: We applied a dual-band hyperspectral SRS microscopy system for imaging tissue sections in both the C-H stretching and fingerprint regions. The same sections were imaged with polarization microscopy for detecting birefringent liquid crystals in the tissues.

Results: Our imaging and analysis pipeline provides accurate classification and quantification of free cholesterol, saturated cholesteryl esters (CEs), unsaturated CE, and triglycerides in liver tissue sections. The subcellular resolution enables investigations of the heterogeneous distribution of saturated CE, which has been under-examined in previous studies. We also discovered that the birefringent crystals, previously found to be associated with NASH development, are predominantly composed of saturated CE.

Conclusions: Our method allows for a detailed characterization of lipid composition in human liver tissues and enables further investigation into the potential mechanism of NASH progression.

Keywords: fibrosing steatohepatitis; human liver tissue; lipid; nonalcoholic fatty liver disease; stimulated Raman scattering microscopy.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Humans
  • Lipids
  • Microscopy, Polarization
  • Non-alcoholic Fatty Liver Disease*
  • Nonlinear Optical Microscopy

Substances

  • Lipids