Direct in vivo gene introduction into rat kidney

Biochem Biophys Res Commun. 1992 Jul 15;186(1):129-34. doi: 10.1016/s0006-291x(05)80784-3.

Abstract

We established a simple and highly efficient method for in vivo gene transfer using HVJ (Sendai virus) and liposomes. Plasmid DNA and high mobility group 1 (HMG1) protein were co-encapsulated in liposomes by agitation and sonication and were co-introduced into cells by HVJ-mediated membrane fusion. pACT SVT DNA, as a reporter gene, was introduced into the kidney of intact rats through a cannula in the renal artery, and SV40 large T antigen was detected by enzyme immunohistochemistry in glomerular cells 4 days after its introduction. This newly developed kidney-directed gene transfer method should be useful not only in basic research but also in potential gene therapeutics of renal diseases.

MeSH terms

  • Actins / genetics
  • Animals
  • Antigens, Polyomavirus Transforming / genetics*
  • Chickens
  • DNA, Viral / administration & dosage
  • DNA, Viral / genetics
  • Drug Carriers
  • Gene Expression
  • Genes, Viral*
  • High Mobility Group Proteins
  • Kidney / physiology*
  • Kidney Glomerulus / cytology
  • Kidney Glomerulus / physiology
  • Kinetics
  • Liposomes
  • Male
  • Membrane Fusion
  • Plasmids
  • Promoter Regions, Genetic
  • Rats
  • Rats, Inbred Strains
  • Simian virus 40 / genetics*
  • Transfection*

Substances

  • Actins
  • Antigens, Polyomavirus Transforming
  • DNA, Viral
  • Drug Carriers
  • High Mobility Group Proteins
  • Liposomes