Expansion of primary human hepatocyte populations by retroviral gene transfer and adenovirus-mediated CRE/LOXP site-specific recombination

N. Kobayashi, H. Noguchi, T. Fujiwara, N. Tanaka, K. A. Westerman, P. Leboulch

Research output: Contribution to journalConference article

Abstract

Human primary hepatocytes are ideal for bioartificial liver (BAL), however, the shortage of human livers available for hepatocyte isolation severely limits the use of this modality. To resolve this issue, adult human hepatocytes were immortalized with a retrovector containing the genes encoding Simian virus 40 T antigen flanked by a pair of Ioxp recombination target that was subsequently excised by Cre recombinase. Based on the observations, a reversible immortalization system in primary adult human hepatocytes was established.

Original languageEnglish
Number of pages1
JournalASAIO Journal
Volume46
Issue number2
DOIs
Publication statusPublished - Jan 1 2000
Event46th Annual Conference and Exposition of ASAIO - New York, NY, USA
Duration: Jun 28 2000Jul 1 2000

ASJC Scopus subject areas

  • Biophysics
  • Bioengineering
  • Biomaterials
  • Biomedical Engineering

Fingerprint Dive into the research topics of 'Expansion of primary human hepatocyte populations by retroviral gene transfer and adenovirus-mediated CRE/LOXP site-specific recombination'. Together they form a unique fingerprint.

Cite this