| Literature DB >> 22943797 |
Hiroshi Yagi1, Ken Fukumitsu, Kazumasa Fukuda, Minoru Kitago, Masahiro Shinoda, Hideaki Obara, Osamu Itano, Shigeyuki Kawachi, Minoru Tanabe, Gina M Coudriet, Jon D Piganelli, Thomas W Gilbert, Alejandro Soto-Gutierrez, Yuko Kitagawa.
Abstract
At this time, the only definitive treatment of hepatic failure is liver transplantation. However, transplantation has been limited by the severely limited supply of human donor livers. Alternatively, a regenerative medicine approach has been recently proposed in rodents that describe the production of three-dimensional whole-organ scaffolds for assembly of engineered complete organs. In the present study, we describe the decellularization of porcine livers to generate liver constructs at a scale that can be clinically relevant. Adult ischemic porcine livers were successfully decellularized using a customized perfusion protocol, the decellularization process preserved the ultrastructural extracellular matrix components, functional characteristics of the native microvascular and the bile drainage network of the liver, and growth factors necessary for angiogenesis and liver regeneration. Furthermore, isolated hepatocytes engrafted and reorganized in the porcine decellularized livers using a human-sized organ culture system. These results provide proof-of-principle for the generation of a human-sized, three-dimensional organ scaffold as a potential structure for human liver grafts reconstruction for transplantation to treat liver disease.Entities:
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Year: 2012 PMID: 22943797 PMCID: PMC3682787 DOI: 10.3727/096368912X654939
Source DB: PubMed Journal: Cell Transplant ISSN: 0963-6897 Impact factor: 4.064