A novel mouse model of in-stent restenosis

Luis Rodriguez-Menocal, Yuntao Wei, Si M. Pham, Melissa St-Pierre, Sen Li, Keith Webster, Pascal Goldschmidt-Clermont, Roberto I. Vazquez-Padron

Research output: Contribution to journalArticlepeer-review

12 Scopus citations


Background and aims: In-stent restenosis (ISR) is the major complication that occurs after percutaneous coronary interventions to facilitate coronary revascularization. Herein we described a simple and cost-effective model, which reproduces important features of ISR in the mouse. Methods and results: Microvascular bare metal stents were successfully implanted in the abdominal aorta of atherosclerotic ApoE-null mice. Patency of implanted stents was interrogated using ultrasound biomicroscopy. Aortas were harvested at different time points after implantation and processed for histopathological analysis. Thrombus formation was histologically detected after 1 day. Leukocyte adherence and infiltration were evident after 7 days and decreased thereafter. Neointimal formation, neointimal thickness and luminal stenosis simultaneously increased up to 28 days after stent implantation. Using multichannel fluorescence molecular tomography (FMT) for spatiotemporal resolution of MMP activities, we observed that MMP activity in the stented aorta of Apo-E null mice was 2-fold higher than that of wild-type mice. Finally, we compared neointimal formation in response to stenting in two genetically different mouse strains. In-stent neointimas in FVB/NJ mice were 2-fold thicker than in C57BL/6J mice (p=0.002). Conclusion: We have developed a model that can take advantage of the multiple genetic resources available for the mouse to study the mechanisms of in-stent restenosis.

Original languageEnglish (US)
Pages (from-to)359-366
Number of pages8
Issue number2
StatePublished - Apr 2010
Externally publishedYes


  • Animal model
  • In-stent restenosis
  • Mouse
  • Stent

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine


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