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The sinusoidal lining cells in "normal" human liver. A scanning electron microscopic investigation
Liver
|April 1, 1986
Summary
Human liver sinusoids show a higher number and porosity of fenestrations in zone 3 compared to zone 1. This zonal difference in fenestrations may impact liver function and transport processes.
Area of Science:
- Hepatology
- Microscopic Anatomy
- Cell Biology
Background:
- Human liver sinusoids are lined by fenestrated endothelial cells, forming a barrier crucial for substance exchange.
- The fenestrations' structure and distribution may vary across different liver zones, influencing sinusoidal permeability.
- Previous studies have suggested zonal heterogeneity in liver sinusoidal structure, but fenestration characteristics require detailed investigation.
Purpose of the Study:
- To quantitatively analyze the fenestrations in human liver sinusoids using scanning electron microscopy.
- To compare the number, size, and porosity of fenestrations between acinar zone 3 and zone 1.
- To investigate potential zonal gradients in sinusoidal permeability.
Main Methods:
- Scanning electron microscopy (SEM) was employed on 13 human liver biopsy samples with normal sinusoidal architecture.
- Fenestrations were counted in acinar zone 3 and zone 1.
- Porosity was estimated using a Texture Analysing System (TAS) on SEM micrographs.
Main Results:
- A significant zonal gradient was observed, with zone 3 exhibiting a higher median number of fenestrations (23.5/µm²) compared to zone 1 (19.2/µm²).
- Sinusoidal porosity increased towards the terminal hepatic vein (9.1% in zone 3 vs. 7.6% in zone 1).
- This increased porosity in zone 3 is attributed to a higher prevalence of fenestrations measuring 100 nm or less in diameter.
Conclusions:
- Human liver sinusoids display zonal heterogeneity in fenestration number and size distribution.
- The observed zonal gradient in fenestrations suggests varying permeability along the sinusoid, potentially influencing blood-hepatocyte transport.
- These findings may have implications for understanding hepatocellular function and metabolic zonation within the liver.