2005
DOI: 10.1007/s00534-005-0986-z
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Hepatocyte transplantation for total liver repopulation

Abstract: Hepatocyte transplantation (HT) is an attractive therapeutic alternative to liver transplantation. A number of experiments have shown the feasibility of total liver parenchymal cell replacement by transplanted hepatocytes. In this review, we would like to highlight researches and clinical reports of HT for liver repopulation. Cellular source of clinical HT should be safety. Immortalized cells, hepatic stem cells, and other stem cells have been used for an experimental model for HT. The exact mechanism of the c… Show more

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Cited by 23 publications
(20 citation statements)
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“…When cultured in vitro, however, they proliferate poorly and divide only a few times [10]. Continuous proliferation could be achieved however by introducing oncogenes, such as Simian virus large tumor antigen (SV40 T) [11]. This often resulted in tumor development [12] together with numerical (aneuploidy) and structural (aberrations) chromosome abnormalities [13].…”
Section: Introductionmentioning
confidence: 98%
“…When cultured in vitro, however, they proliferate poorly and divide only a few times [10]. Continuous proliferation could be achieved however by introducing oncogenes, such as Simian virus large tumor antigen (SV40 T) [11]. This often resulted in tumor development [12] together with numerical (aneuploidy) and structural (aberrations) chromosome abnormalities [13].…”
Section: Introductionmentioning
confidence: 98%
“…So far, animal transplantation models oVer unique opportunities to investigate the mechanisms of both the integration and interaction of transplanted hepatocytes with host liver cells (Mizuguchi et al 2005). Hepatocytes are metabolically specialised cells displaying distinctive gene expression patterns within the liver lobule.…”
Section: Introductionmentioning
confidence: 99%
“…One likely reason during the dedifferentiation step could be simply Hepatocyte transplantation is a promising alternative to whole-organ transplantation either to bridge patients described by a graft versus host reaction (7,11) of the cells towards the applied human type AB sera or FCS. awaiting a donor liver or to correct at least temporarily genetic deficiencies of the liver (19,27,29,33,34,38,40).…”
Section: Highest Phase I and Ii Enzyme Activitiesmentioning
confidence: 99%