TY - JOUR
T1 - Human-scale whole-organ bioengineering for liver transplantation
T2 - A regenerative medicine approach
AU - Yagi, Hiroshi
AU - Fukumitsu, Ken
AU - Fukuda, Kazumasa
AU - Kitago, Minoru
AU - Shinoda, Masahiro
AU - Obara, Hideaki
AU - Itano, Osamu
AU - Kawachi, Shigeyuki
AU - Tanabe, Minoru
AU - Coudriet, Gina M.
AU - Piganelli, Jon D.
AU - Gilbert, Thomas W.
AU - Soto-Gutierrez, Alejandro
AU - Kitagawa, Yuko
PY - 2013
Y1 - 2013
N2 - 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.
AB - 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.
KW - Bile duct
KW - Bioengineering in organ transplantation
KW - Decellularization
KW - Liver tissue engineering
KW - Porcine liver
KW - Regenerative medicine
KW - Whole-organ scaffold
UR - http://www.scopus.com/inward/record.url?scp=84874385456&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84874385456&partnerID=8YFLogxK
U2 - 10.3727/096368912X654939
DO - 10.3727/096368912X654939
M3 - Article
C2 - 22943797
AN - SCOPUS:84874385456
SN - 0963-6897
VL - 22
SP - 231
EP - 242
JO - Cell Transplantation
JF - Cell Transplantation
IS - 2
ER -