6533b829fe1ef96bd1289989

RESEARCH PRODUCT

Nonparenchymal cells in chronically hyperinsulinemic liver acini of diabetic rats, with special regard to hepatic stellate cells

Frank DombrowskiUlrich PfeiferPeter SchirmacherMatthias Evert

subject

Malemedicine.medical_specialtyLiver cytologymedicine.medical_treatmentIslets of Langerhans TransplantationIn situ hybridizationBiologyDiabetes Mellitus ExperimentalAcinusHyperinsulinismInternal medicinemedicineAnimalsIn Situ Hybridizationgeographygeography.geographical_feature_categoryHepatologyHepatocyte Growth FactorGrowth factorIsletRatsTransplantationMicroscopy ElectronEndocrinologymedicine.anatomical_structureLiverRats Inbred LewChronic DiseaseLinear ModelsHepatic stellate cellHepatocyte growth factorCell Divisionmedicine.drug

description

Abstract Background/Aims: An increase in proliferative activity and other distinct hepatocellular alterations — resembling preneoplastic foci and progressing to hepatocellular tumors — have been shown to develop in liver acini draining the blood from islets of Langerhans, transplanted through the portal vein into the liver of streptozotocin-diabetic rats. Methods: Altered and unaltered liver acini were investigated for possible changes in hepatic stellate cells 4–76 days after islet transplantation. Results: Corresponding to a significant increase in the hepatocellular volume, the volume density of total non-parenchymal cells was significantly reduced in altered compared to unaltered liver acini. With regard to the total nonparenchymal cell volume, the hepatic stellate cell fraction was not different, whereas the fraction of Kupffer cells was significantly reduced and the fraction of sinusoidal endothelial cells was significantly increased in altered compared to unaltered liver acini, respectively. The volume density as well as the single volume of the hepatic stellate cell mitochondria increased significantly in altered compared to unaltered liver acini. Hepatic stellate cell lipid droplets did not show significant differences between altered and unaltered liver acini. In situ hybridization for hepatocyte growth factor mRNA showed no differences in intensity of the specific signals in hepatic stellate cells of altered versus unaltered liver acini. The transplanted islets were negative for hepatic growth factor mRNA. Conclusions: The results suggest that hepatic growth factor production by hepatic stellate cells or by islet cells is not relevant to hepatocellular proliferative activity in altered liver acini.

https://doi.org/10.1016/s0168-8278(98)80296-1