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pubmed-article:7597103pubmed:abstractTextRetrovirus-mediated gene transfer into hepatocytes in vivo results in long-term gene expression. Limitations include the need to remove two-thirds of the liver and the relatively low frequency of gene transfer. To increase gene transfer without surgical hepatectomy, mouse hepatocytes were transduced in vivo with a recombinant adenovirus that transiently expressed urokinase, resulting in high rates of asynchronous liver regeneration. During the regenerative phase, in vivo retroviral-mediated gene transfer in hepatocytes resulted in 5- to 10-fold greater transduction efficiencies than that obtained by conventional partial hepatectomy. In 3-4 weeks, the architecture and microscopic structure of the recipient livers were normal. The two-viral system of achieving permanent transgene expression from hepatocytes in vivo offers an alternative approach to current ex vivo and in vivo gene-transfer models.lld:pubmed
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pubmed-article:7597103pubmed:articleTitleAdenovirus-mediated urokinase gene transfer induces liver regeneration and allows for efficient retrovirus transduction of hepatocytes in vivo.lld:pubmed
pubmed-article:7597103pubmed:affiliationMarkey Molecular Medicine Center, Department of Medicine, University of Washington, Seattle 98195, USA.lld:pubmed
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pubmed-article:7597103pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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