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Figure 2 | Comparative Hepatology

Figure 2

From: Comparison of different methods to obtain and store liver biopsies for molecular and histological research

Figure 2

Liver histology. A) Normal liver, dog #1, portal area and periportal parenchyma. The tissue architecture is well preserved, with good contrast and sufficient cellular morphology reflected in distinct cellular and nuclear membranes, and sufficient cytoplasmic details. Needle biopsy, 1 h formalin fixation, HE staining, bar 50 μm. B) Normal liver, dog #5, portal area with bile duct (arrow) and periportal parenchyma. The tissue is well conserved, and there is mild cellular pronounciation and slightly enhanced eosinophilic appearance of all cells save erythrocytes. Needle biopsy, 8 hrs Boonfix fixation at room temperature, HE staining, bar 50 μm. C) Normal liver, dog #5, portal area and periportal parenchyma. Insufficient conservation of tissue architecture in the central part of the biopsy, to the right hand side of the arrow, with ill defined cellular borders, strong eosinophilia and shrinkage of hepatocytes, pycnotic nuclei and artificially widened sinusoids. Needle biopsy, 8 hrs RNAlater fixation at room temperature, HE staining, bar 50 μm. D) Copper related chronic active hepatitis, dog #9, parenchyma, control tissue. Many, black staining copper granules appear in the cytoplasm of hepatocytes and Kupffer cells. Wedge biopsy, 24 hrs formalin fixation, rhodanine acid stain, bar 50 μm. E) Liver with copper storage, dog #6, parenchyma. Intracytoplasmic copper granules stain yellow-brown, therefore no reliable differentiation between copper and lipofuscin granules can be made. Needle biopsy, 8 hrs Boonfix fixation, rubeanic acid stain, bar 50 μm. F) Normal liver, dog #2, portal area and periportal parenchyma. Cholangiocytes in the portal tract (asterisk) display a strong signal (brown) in the cytoplasm with negligable aspecific background staining. Also, the parenchyma contains one small, isolated positive periportal cell (arrow), interpreted as a progenitor cell. Needle biopsy, 1 h formalin fixation, K-7 immunohistochemistry, bar 20 μm. G) Normal liver, dog #5, portal area and periportal parenchyma. All hepatocytes feature strong cytoplasmic reactivity, all other cells are negative. Needle biopsy, 1 h formalin fixation, Hepar1 immunostaining, bar 50 μm. H) Normal liver, dog #8, parenchyma, control tissue. Strong signal (brown) is elicited along the canalicular membranes of all hepatocytes, insignificant background staining. Wedge biopsy, 24 hrs formalin fixation, MRP-2 immunostaining, bar 20 μm.

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