Characterization of glycosaminoglycans in regenerating canine liver

J Hepatol. 1997 May;26(5):1135-40. doi: 10.1016/s0168-8278(97)80123-7.

Abstract

Background/aims: Liver regeneration after partial hepatectomy is accompanied by hepatocyte proliferation and alteration of the extracellular matrix. Glycosaminoglycans, which are components of the extracellular matrix, interact with other matrix components, and are related to hepatocyte growth. The aim of this study was to investigate the relationship between hepatocyte proliferation and changes in glycosaminoglycan.

Methods: Hepatocyte proliferation and changes in glycosaminoglycan were investigated in dogs after 55% partial hepatectomy. Hepatocyte mitosis was investigated by immunohistochemistry using anti-proliferating cell nuclear antigen antibody. The amount of glycosaminoglycan was determined by the carbazole-sulfuric acid method. We used a new method for analysis of glycosaminoglycan chains, involving endo-beta-xylosidase digestion and fluorescence labelling, to investigate the components of glycosaminoglycan.

Results: Hepatocyte mitosis was increased after hepatectomy, reaching a peak at postoperative day 7. The total amount of hepatic glycosaminoglycan reached a maximum at 1 to 2 weeks afer hepatectomy, and the ratio of the components showed a concomitant change, the amount of heparan sulfate increasing, and that of chondroitin sulfate/dermatan sulfate decreasing. Increased heparan sulfate has shorter chains at 1 to 2 weeks after hepatectomy.

Conclusions: These results suggest that the transient changes in heparan sulfate with a decreased chain length and chondroitin sulfate/dermatan sulfate and observed during liver regeneration are associated with hepatocyte proliferation.

MeSH terms

  • Animals
  • Biocompatible Materials
  • Cell Division
  • Cellulose / analogs & derivatives
  • Chromatography, High Pressure Liquid
  • Dogs
  • Electrophoresis, Gel, Two-Dimensional
  • Glycosaminoglycans / metabolism*
  • Heparitin Sulfate / metabolism
  • Hepatectomy / methods
  • Liver / cytology
  • Liver / metabolism*
  • Liver Regeneration*
  • Membranes, Artificial

Substances

  • Biocompatible Materials
  • Glycosaminoglycans
  • Membranes, Artificial
  • acetylcellulose
  • Cellulose
  • Heparitin Sulfate