Liver tissue engineering at extrahepatic sites in mice as a potential new therapy for genetic liver diseases

• Published in: Hepatology (Baltimore, Md.) Vol. 41; no. 1; pp. 132 - 140
• Main Authors: OHASHI, Kazuo, WAUGH, Jacob M, DAKE, Michael D, YOKOYAMA, Takashi, KUGE, Hiroyuki, NAKAJIMA, Yoshiyuki, YAMANOUCHI, Masaki, NAKA, Hiroyuki, YOSHIOKA, Akira, KAY, Mark A
• Format: Journal Article
• Language: English
• Published: Hoboken, NJ Wiley 2005
• Subjects: alpha 1-Antitrypsin - genetics; alpha 1-Antitrypsin - metabolism; Angiogenic Proteins - administration & dosage; Angiogenic Proteins - therapeutic use; Animals; Biological and medical sciences; Cell Survival; Factor VIII - metabolism; Fibroblast Growth Factor 1 - administration & dosage; Fibroblast Growth Factor 1 - therapeutic use; Fundamental and applied biological sciences. Psychology; Gastroenterology. Liver. Pancreas. Abdomen; Hemophilia A - blood; Hemophilia A - surgery; Hemophilia A - therapy; Hepatocytes - metabolism; Hepatocytes - transplantation; Humans; Liver - pathology; Liver - physiopathology; Liver Regeneration; Liver, biliary tract, pancreas, portal circulation, spleen; Liver. Bile. Biliary tracts; Liver. Biliary tract. Portal circulation. Exocrine pancreas; Medical sciences; Mice; Mice, Inbred Strains; Mice, Transgenic; Microspheres; Other diseases. Semiology; Preoperative Care; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases; Surgery of the digestive system; Tissue Engineering; Transplantation, Heterotopic; Vertebrates: digestive system; Prognosis; Hepatic disease; Hemopathy; Extract; Bleeding time; Kidney; Tissue; Liver failure; Hepatocyte; Blood vessel; Network; Graft; Extracellular matrix; Subcutaneous; Rodentia; Capsule; Survival; Hemophilia A; Genetic disease; Regeneration; Vertebrata; Mammalia; Treatment; Mouse; Animal; Digestive diseases; Gene therapy; Coagulopathy; Organ; Liver transplantation
• ISSN: 0270-9139; 1527-3350
• DOI: 10.1002/hep.20484

Liver tissue engineering using hepatocyte transplantation has been proposed as an alternative to whole-organ transplantation or liver-directed gene therapy to correct various types of hepatic insufficiency. Hepatocytes are not sustained when transplanted under the kidney capsule of syngeneic mice. However, when we transplanted hepatocytes with the extracellular matrix components extracted from Engelbreth-Holm-Swarm cells, hepatocytes survived for at least 140 days and formed small liver tissues. Liver engineering in hemophilia A mice reconstituted 5% to 10% of normal clotting activity, enough to reduce the bleeding time and have a therapeutic benefit. Conversely, the subcutaneous space did not support the persistent survival of hepatocytes with Engelbreth-Holm-Swarm gel matrix. We hypothesized that establishing a local vascular network at the transplantation site would reduce graft loss. To test this idea, we provided a potent angiogenic agent before hepatocyte transplantation into the subcutaneous space. With this procedure, persistent survival was achieved for the length of the experiment (120 days). To establish that these engineered liver tissues also retained their native regeneration potential in vivo, we induced two different modes of proliferative stimulus to the naive liver and confirmed that hepatocytes within the extrahepatic tissues regenerated with activity similar to that of naive liver. In conclusion, our studies indicate that liver tissues can be engineered and maintained at extrahepatic sites, retain their capacity for regeneration in vivo, and used to successfully treat genetic disorders.