Which hepatocyte will it be? Hepatocyte choice for bioartificial liver support systems
Open Access
- 1 January 2001
- journal article
- review article
- Published by Wolters Kluwer Health in Liver Transplantation
- Vol. 7 (1), 2-10
- https://doi.org/10.1053/jlts.2001.20845
Abstract
Liver failure, notwithstanding advances in medical management, remains a cause of considerable morbidity and mortality in the developed world. Although bioartificial liver (BAL) support systems offer the potential of significant therapeutic benefit for such patients, many issues relating to their use are still to be resolved. In this review, these issues are examined in terms of the functions required, the cells of choice in such a system, and the most appropriate environment to optimize the function of such cells. The major functions identified to date for a BAL are ammonia detoxification and biotransformation of toxic compounds, although this somewhat belies the complexity of the functions required. Two practical choices for cell type within such a system are xenogenic hepatocytes and immortalized human hepatocyte lines. Both these choices have drawbacks, such as the transmission of zoonoses and malignant infiltration, respectively. Finally, improvements in culture conditions, such as supplemented media, biodegradable scaffolds, and coculture, offer the possibility of prolonging the differentiated function of hepatocytes in a BAL.Keywords
This publication has 80 references indexed in Scilit:
- Xenotransplantation: A summary of the international business communications' fourth international congressLiver Transplantation, 2000
- Xenotransplantation: postponed by a millennium?QJM: An International Journal of Medicine, 2000
- Influence of human fulminant hepatic failure sera on endogenous retroviral expression in pig hepatocytesLiver Transplantation, 2000
- Evaluation of a novel bioartificial liver in rats with complete liver ischemia: treatment efficacy and species-specific α-GST detection to monitor hepatocyte viabilityJournal of Hepatology, 1999
- The peroxisome proliferators are hepatocyte mitogens in chemically- defined media: glucocorticoid-induced PPAR alpha is linked to peroxisome proliferator mitogenesisCarcinogenesis: Integrative Cancer Research, 1998
- Establishment of a Human Hepatocyte Line Derived from Primary Culture in a Collagen Gel Sandwich Culture SystemExperimental Cell Research, 1995
- A Novel Bioreactor Design for In Vitro Reconstruction of In Vivo Liver CharacteristicsArtificial Organs, 1995
- Characterization of human hepatocyte lines derived from normal liver tissueHepatology, 1994
- Development of a Hybrid Bioartificial LiverAnnals of Surgery, 1993
- Optimization of Cryopreservation Procedures for Rat and Human HepatocytesXenobiotica, 1989