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From a Single Cell to a Whole Human Liver: Disease Modeling and Transplantation.
Motomura, Takashi; Faccioli, Lanuza A P; Diaz-Aragon, Ricardo; Kocas-Kilicarslan, Zehra N; Haep, Nils; Florentino, Rodrigo M; Amirneni, Sriram; Cetin, Zeliha; Peri, Bhaavna S; Morita, Kazutoyo; Ostrowska, Alina; Takeishi, Kazuki; Soto-Gutierrez, Alejandro; Tafaleng, Edgar N.
Afiliação
  • Motomura T; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Faccioli LAP; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Diaz-Aragon R; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Kocas-Kilicarslan ZN; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Haep N; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Florentino RM; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Amirneni S; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Cetin Z; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Peri BS; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Morita K; Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Ostrowska A; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Takeishi K; Pittsburgh Liver Research Center, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Soto-Gutierrez A; Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Tafaleng EN; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Semin Liver Dis ; 42(4): 413-422, 2022 11.
Article em En | MEDLINE | ID: mdl-36044927
ABSTRACT
Although the underlying cause may vary across countries and demographic groups, liver disease is a major cause of morbidity and mortality globally. Orthotopic liver transplantation is the only definitive treatment for liver failure but is limited by the lack of donor livers. The development of drugs that prevent the progression of liver disease and the generation of alternative liver constructs for transplantation could help alleviate the burden of liver disease. Bioengineered livers containing human induced pluripotent stem cell (iPSC)-derived liver cells are being utilized to study liver disease and to identify and test potential therapeutics. Moreover, bioengineered livers containing pig hepatocytes and endothelial cells have been shown to function and survive after transplantation into pig models of liver failure, providing preclinical evidence toward future clinical applications. Finally, bioengineered livers containing human iPSC-derived liver cells have been shown to function and survive after transplantation in rodents but require considerable optimization and testing prior to clinical use. In conclusion, bioengineered livers have emerged as a suitable tool for modeling liver diseases and as a promising alternative graft for clinical transplantation. The integration of novel technologies and techniques for the assembly and analysis of bioengineered livers will undoubtedly expand future applications in basic research and clinical transplantation.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Falência Hepática / Células-Tronco Pluripotentes Induzidas / Hepatopatias Limite: Animals / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Falência Hepática / Células-Tronco Pluripotentes Induzidas / Hepatopatias Limite: Animals / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article