Established neointimal hyperplasia in vein grafts expands via TGF-beta-mediated progressive fibrosis

Am J Physiol Heart Circ Physiol. 2009 Oct;297(4):H1200-7. doi: 10.1152/ajpheart.00268.2009. Epub 2009 Jul 17.

Abstract

In weeks to months following implantation, neointimal hyperplasia (NIH) in vein grafts (VGs) transitions from a cellularized to a decellularized phenotype. The inhibition of early cellular proliferation failed to improve long-term VG patency. We have previously demonstrated that transforming growth factor-beta(1) (TGF-beta(1))/connective tissue growth factor (CTGF) pathways mediate a conversion of fibroblasts to myofibroblasts in the early VG (<2 wk). We hypothesize that these similar pathways drive fibrosis observed in the late VG lesion. Within rabbit VGs, real-time RT-PCR, Western blot analysis, ELISA, and immunohistochemistry were used to examine TGF-beta/CTGF pathways in late (1-6 mo) NIH. All VGs exhibited a steady NIH growth (P = 0.006) with significant reduction in cellularity (P = 0.01) over time. Substantial TGF-beta profibrotic activities, as evidenced by enhanced TGF-beta(1) activation, TGF-beta receptor types I (activin receptor-like kinase 5)-to-II receptor ratio, SMAD2/3 phosphorylation, and CTGF production, persisted throughout the observation period. An increased matrix synthesis was accompanied by a temporal reduction of matrix metalloproteinase-2 (P = 0.001) and -9 (P < 0.001) activity. VG NIH is characterized by a conversion from a proproliferative to a profibrotic morphology. An enhanced signaling via TGF-beta/CTGF coupled with reduced matrix metalloproteinase activities promotes progressive fibrotic NIH expansion. The modulation of late TGF-beta/CTGF signaling may offer a novel therapeutic strategy to improve the long-term VG durability.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carotid Artery, Common / metabolism*
  • Carotid Artery, Common / pathology
  • Carotid Artery, Common / surgery
  • Cell Proliferation*
  • Connective Tissue Growth Factor / metabolism
  • Constriction, Pathologic
  • Disease Models, Animal
  • Fibrosis
  • Graft Occlusion, Vascular / metabolism*
  • Graft Occlusion, Vascular / pathology
  • Graft Occlusion, Vascular / physiopathology
  • Hyperplasia
  • Jugular Veins / transplantation*
  • Male
  • Matrix Metalloproteinase 2 / metabolism
  • Matrix Metalloproteinase 9 / metabolism
  • Microdissection
  • Phosphorylation
  • Protein Serine-Threonine Kinases / metabolism
  • Rabbits
  • Receptor, Transforming Growth Factor-beta Type I
  • Receptor, Transforming Growth Factor-beta Type II
  • Receptors, Transforming Growth Factor beta / metabolism
  • Signal Transduction
  • Smad2 Protein / metabolism
  • Smad3 Protein / metabolism
  • Time Factors
  • Transforming Growth Factor beta1 / genetics
  • Transforming Growth Factor beta1 / metabolism*
  • Tunica Intima / metabolism*
  • Tunica Intima / pathology
  • Tunica Intima / surgery
  • Vascular Patency

Substances

  • Receptors, Transforming Growth Factor beta
  • Smad2 Protein
  • Smad3 Protein
  • Transforming Growth Factor beta1
  • Connective Tissue Growth Factor
  • Protein Serine-Threonine Kinases
  • Receptor, Transforming Growth Factor-beta Type I
  • Receptor, Transforming Growth Factor-beta Type II
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9