Adeno-associated virus vector-mediated production of hepatocyte growth factor attenuates liver fibrosis in mice View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2007-12-22

AUTHORS

Kazuhiro Suzumura, Tadamichi Hirano, Gakuhei Son, Yuji Iimuro, Hiroaki Mizukami, Keiya Ozawa, Jiro Fujimoto

ABSTRACT

PurposeAdeno-associated virus (AAV) vectors can achieve long-term gene expression and are now feasible for use in human gene therapy. We constructed hepatocyte growth factor (HGF) expressing AAV (AAV5-HGF) and examined its effect in two mouse hepatic fibrosis models.MethodsA model of hepatic fibrosis was established by carbon tetrachloride (CCl4) administration in Balb/c mice. After the establishment of liver fibrosis, AAV5-HGF was injected once into the portal vein. Mice were killed 3, 6, 9, and 12 weeks after injection. Another model was established by bile duct ligation (BDL). Seven weeks after AAV5-HGF injection, mice underwent BDL, and were then killed 2 weeks after BDL.ResultsMice that received AAV5-HGF achieved stable HGF expression both in the serum and liver for at least 12 weeks. In both models, significant improvement of the liver fibrosis was found in all mice receiving AAV5-HGF based on Azan-Mallory staining. Suppression of hepatic stellate cells (HSC) was confirmed by immunohistochemistry. Fibrogenic markers were significantly suppressed and collagenase activity increased in the livers of mice receiving AAV5-HGF.ConclusionsA single injection of AAV vector containing HGF gene achieved long-term expression of HGF and resulted in resolution of mouse liver fibrosis. HGF gene therapy mediated by AAV is feasible for the treatment of liver fibrosis. More... »

PAGES

80-88

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s12072-007-9042-1

DOI

http://dx.doi.org/10.1007/s12072-007-9042-1

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1037116756

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/19669282


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