Effect on vein graft intimal hyperplasia of nuclear factor-kB decoy transfection using the second generation of HVJ vector

J Cardiovasc Surg (Torino). 2007 Aug;48(4):463-70.

Abstract

Aim: Vein graft stenosis due to intimal hyperplasia (IH) is the main cause of graft failure. We examined possibilities of nuclear factor-kB (NF-kB) expression in vein grafts, and inhibitive effects of NF-kB decoy on the gene expression and subsequent vein graft IH.

Methods: Fifteen mongrel dogs underwent femoral artery replacement with autogenous vein grafts. Group I: grafts were retrieved at a predetermined time and subjected to NF-kB binding activity assay; Groups II and III: grafts were transfected with scrambled (II-a, III-a) or NF-kB (II-b, III-b) decoy using hemagglutinating virus of Japan envelope before implantation. Grafts were retrieved 7 days after implantation for evaluation of intercellular adhesion molecule-1 (ICAM-1) mRNA expression (Group II) and 4 weeks after implantation for comparison of IH by morphometric analysis (Group III).

Results: NF-kB binding activity was increased in a time-dependent manner, with a peak 2 days after implantation. The ratio between ICAM-1 and glyceraldehyde-3-phosphate dehydrogenase mRNA expression in II-b was significantly lower than that in II-a (0.347 +/- 0.07 versus 0.612+/-0.08; P = 0.047). The ratio of intimal cross-section area to luminal cross-section area of III-b was significantly lower than that of the III-a (0.096+/-0.03 versus 0.461+/-0.11; P = 0.048).

Conclusion: NF-kB binding activity in vein grafts increases after implantation, and transfection of NF-kB decoy before implantation may reduce IH through the inhibition of ICAM-1 expression.

MeSH terms

  • Animals
  • Dogs
  • Femoral Artery / surgery*
  • Genetic Vectors
  • Hyperplasia / etiology
  • Hyperplasia / metabolism
  • NF-kappa B / physiology*
  • Oligonucleotides
  • RNA, Messenger / metabolism
  • Saphenous Vein / metabolism
  • Saphenous Vein / pathology*
  • Saphenous Vein / transplantation*
  • Sendai virus
  • Transfection
  • Tunica Intima / metabolism*
  • Tunica Intima / pathology*

Substances

  • NF-kappa B
  • Oligonucleotides
  • RNA, Messenger