Extracellular matrix proteins, integrin receptors (VLA-beta 1, VLA-alpha 2 and VLA-alpha 5) and growth fraction in atypical macroregenerative nodules of the liver: an immunocytochemical case study

Histochemistry. 1994 Aug;102(1):29-36. doi: 10.1007/BF00271046.

Abstract

A case of cirrhotic liver harbouring three atypical macroregenerative nodules and an hepatocellular carcinoma was immunocytochemically investigated for the expression of VLA-beta 1, VLA-alpha 2 and VLA-alpha 5 integrins and for different extracellular matrix (ECM) components (collagen I, collagen IV, laminin, fibronectin and tenascin). In addition, the proliferative activity within the nodules was evaluated, using the MIB 1 monoclonal antibody (MAb). The cirrhotic liver disclosed a continuous staining pattern of the ECM proteins investigated, as well as a "sinusoidal" immunostaining of VLA-beta 1, VLA-alpha 2 and VLA-alpha 5. The macroregenerative nodules showed a discontinued immunoreactivity for ECM proteins while maintaining a VLA-beta 1 sinusoidal immunostaining, coupled with intercellular immunostaining. VLA-alpha 2 and VLA-alpha 5 expression was lacking. The growth fraction was low in both the above pathological conditions. The hepatocellular carcinoma was devoid of any ECM immunostaining. VLA-beta 1 immunoreactivity exhibited a honeycomb pattern of staining, whereas VLA alpha subunits were absent. MIB1 expression was high, being present in 30% of neoplastic nuclei. A possible relationship between atypical macroregenerative nodules and hepatocellular carcinoma is discussed.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Hepatocellular / chemistry*
  • Carcinoma, Hepatocellular / pathology*
  • Cell Adhesion Molecules / physiology
  • Cell Division / physiology
  • Extracellular Matrix Proteins / analysis*
  • Humans
  • Immunohistochemistry
  • Integrins / analysis*
  • Liver Cirrhosis / metabolism*
  • Liver Cirrhosis / pathology*
  • Liver Neoplasms / chemistry*
  • Liver Neoplasms / pathology*
  • Liver Regeneration*
  • Neoplasm Proteins / analysis*
  • Phenotype

Substances

  • Cell Adhesion Molecules
  • Extracellular Matrix Proteins
  • Integrins
  • Neoplasm Proteins