1. ¹1st Institute of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary
2. ²Department of Gastroenterology and Endocrinology, Georg August University of Göttingen, Göttingen, Germany
3. ³2nd Institute of Pathology, Semmelweis University, Budapest, Hungary

Correspondence: P Tátrai, MSc, 1st Institute of Pathology and Experimental Cancer Research, Semmelweis University, Ülli út 26, H-1085, Budapest, Hungary. E-mail: tatpeter@korb1.sote.hu

Received 22 March 2006; Accepted 10 August 2006; Published online 18 September 2006.

Abstract

Agrin is a multifunctional heparan sulfate proteoglycan originally discovered in the neuromuscular junctions and later observed in numerous other localizations. The presence of agrin in the liver, either healthy or diseased, has formerly not been reported. We detected agrin in minor amounts in the basement membranes of blood vessels and bile ducts in the healthy liver. The proliferation of bile ductules and the formation of new septal blood vessels in liver cirrhosis, as well as neoangiogenesis in the hepatocellular carcinoma (HCC) result in a dramatic increase in the quantity of agrin. Vascular and peribiliary basement membranes were strongly immunopositive for agrin in 29/29 human liver specimens with cirrhosis and HCC. However, sinusoidal walls of regenerative nodules in the cirrhotic liver consistently remained negative. Given the selectivity of agrin for tumor microvessels, agrin immunohistochemistry may prove helpful in recognizing malignant transformation in cirrhotic livers. Similar immunohistochemical observations were made on the liver of rats exposed to a combined cirrhosis/HCC induction treatment. In both human and rats, agrin probably originates from activated myofibroblasts, vascular smooth muscle cells and biliary epithelial cells. Increased agrin expression in human specimens, in the liver of 4/4 treated rats, as well as in isolated rat liver mesenchymal cells was verified by quantitative RT-PCR. Considering that agrin binds various growth factors, and it directly interacts with cell membrane receptors such as _v-integrins, we hypothesize a stimulatory role for agrin in neoangiogenic processes such as tumor vascularization, and a supportive role in bile ductule proliferation.