Molecular Therapy: Nucleic Acids (Jan 2016)

Effects of Fibrotic Tissue on Liver-targeted Hydrodynamic Gene Delivery

  • Yuji Kobayashi,
  • Kenya Kamimura,
  • Hiroyuki Abe,
  • Takeshi Yokoo,
  • Kohei Ogawa,
  • Yoko Shinagawa-Kobayashi,
  • Ryo Goto,
  • Ryosuke Inoue,
  • Masato Ohtsuka,
  • Hiromi Miura,
  • Tsutomu Kanefuji,
  • Takeshi Suda,
  • Masanori Tsuchida,
  • Yutaka Aoyagi,
  • Guisheng Zhang,
  • Dexi Liu,
  • Shuji Terai

DOI
https://doi.org/10.1038/mtna.2016.63
Journal volume & issue
Vol. 5, no. C

Abstract

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Hydrodynamic gene delivery is a common method for gene transfer to the liver of small animals, and its clinical applicability in large animals has been demonstrated. Previous studies focused on functional analyses of therapeutic genes in animals with normal livers and little, however, is known regarding its effectiveness and safety in animals with liver fibrosis. Therefore, this study aimed to examine the effects of liver fibrosis on hydrodynamic gene delivery efficiency using a rat liver fibrosis model. We demonstrated for the first time, using pCMV-Luc plasmid, that this procedure is safe and that the amount of fibrotic tissue in the liver decreases gene delivery efficiency, resulting in decrease in luciferase activity depending on the volume of fibrotic tissue in the liver and the number of hepatocytes that are immunohistochemically stained positive for transgene product. We further demonstrate that antifibrotic gene therapy with matrix metalloproteinase-13 gene reduces liver fibrosis and improves efficiency of hydrodynamic gene delivery. These results demonstrate the negative effects of fibrotic tissue on hydrodynamic gene delivery and its recovery by appropriate antifibrotic therapy.

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