Vascular endothelial growth factor reduces Fas-mediated acute liver injury in mice

• Published in: Journal of gastroenterology and hepatology Vol. 23; no. 7pt2; pp. e207 - e211
• Main Authors: Tanaka, Yoichi, Sohda, Tetsuro, Matsuo, Katsuhiko, Anan, Akira, Irie, Makoto, Takeyama, Yasuaki, Iwata, Kaoru, Shakado, Satoshi, Sakisaka, Shotaro
• Format: Journal Article
• Language: English
• Published: Melbourne, Australia Blackwell Publishing Asia 01.07.2008
• Subjects: Alanine Transaminase - blood; Animals; Antibodies; Apoptosis; bcl-X Protein - metabolism; Disease Models, Animal; endothelial cells; fas Receptor - immunology; fas Receptor - metabolism; fulminant liver failure; Hepatocyte Growth Factor - metabolism; Humans; Injections, Intraperitoneal; Liver - immunology; Liver - metabolism; Liver - pathology; Liver Failure, Acute - immunology; Liver Failure, Acute - metabolism; Liver Failure, Acute - pathology; Liver Failure, Acute - prevention & control; Male; Mice; Mice, Inbred BALB C; Recombinant Proteins - metabolism; vascular endothelial growth factor; Vascular Endothelial Growth Factor A - administration & dosage; Vascular Endothelial Growth Factor A - metabolism
• ISSN: 0815-9319; 1440-1746
• DOI: 10.1111/j.1440-1746.2007.05135.x

Background and Aim:  Fulminant hepatitis is still a fatal liver disease, and no specific treatment for it has been available. Vascular endothelial growth factor (VEGF) is the focus of attention because of its various actions. We investigated the effect of vascular endothelial growth factor (VEGF) on Fas‐induced fulminant hepatic failure (FHF). Method:  Male Balb/c mice were treated with an intraperitoneal injection of an anti‐Fas antibody (Jo‐2 Ab) with or without premedication with intraperitoneally administered human recombinant VEGF. Results:  The serum level of alanine aminotransferase (ALT) was up to 300 times higher that of normal mice following the Jo‐2 Ab injection, and histological analysis revealed hepatic injury and massive hepatocyte apoptosis. The VEGF significantly suppressed an elevation in serum ALT levels and hepatocyte apoptosis. Immunohistochemically, VEGF‐treated mice showed that Bcl‐xL in hepatocytes was strongly expressed. Conclusions:  Since hepatocytes do not express VEGF receptors, we speculated that VEGF acts on sinusoidal endothelial cells (SECs) and promotes production of cytokines such as hepatocyte growth factor in SECs, resulting in reducing apoptosis through an increase expression of Bcl‐xL in hepatocytes. We suggest that VEGF has a potent antiapoptotic effect on hepatocytes through cell–cell interaction between SECs and hepatocytes.