The transcription factor ETS-1 mediates proinflammatory responses and neointima formation in carotid artery endoluminal vascular injury

Hypertension. 2010 Jun;55(6):1381-8. doi: 10.1161/HYPERTENSIONAHA.110.150995. Epub 2010 Apr 5.

Abstract

The transcription factor ETS-1 is a critical mediator of vascular inflammation and hypertrophy in hypertension. We tested the hypothesis that ETS-1 is a mediator of proinflammatory responses and neointimal hyperplasia after balloon injury of the carotid artery. For this study, we took advantage of the availability of an ETS-1 dominant-negative (DN) peptide. Sprague-Dawley rats were assigned to treatment with ETS-1 DN, a mutant peptide (ETS-1 MU), or vehicle (Veh) and subjected to balloon injury of the carotid artery. After 2, 24 hours, and 14 days, the rats were euthanized, and both carotid arteries were processed for real-time polymerase chain reaction (2 hours), immunofluorescence and immunohistochemistry (24 hours), and morphometric analysis (14 days). ETS-1 mRNA was up regulated (2.4-fold) in injured carotid arteries. By immunofluorescence, we confirmed increased nuclear expression of ETS-1 24 hours postinjury. The carotid artery mRNA expression of monocyte chemotactic protein-1, cytokine-induced neutrophil chemoattractant-2, P-selectin, E-selectin, vascular cell adhesion molecule, and intercellular adhesion molecule was increased 2 hours after injury. ETS-1 DN but not ETS-1 MU significantly reduced mRNA and protein expression for monocyte chemotactic protein-1, P-selectin, and E-selectin in injured arteries. These changes were accompanied by concomitant reductions in vascular monocyte and leukocyte infiltration. Moreover, treatment with ETS-1 DN but not ETS-1 MU resulted in a 50% reduction in neointima formation at day 14 after balloon injury. This study unveils the role of ETS-1 as a mediator of inflammation and neointima formation in a model of carotid artery balloon injury and may result in the development of novel strategies in the treatment of vascular injury.

Publication types

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

MeSH terms

  • Analysis of Variance
  • Animals
  • Biomarkers / metabolism
  • Carotid Artery Injuries / drug therapy
  • Carotid Artery Injuries / metabolism
  • Carotid Artery Injuries / pathology*
  • Catheterization
  • Chemokine CCL2 / metabolism
  • Cytokines / drug effects
  • Cytokines / metabolism*
  • Disease Models, Animal
  • E-Selectin / metabolism
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / pathology*
  • Fluorescent Antibody Technique
  • Immunohistochemistry
  • Injections, Intraperitoneal
  • Male
  • P-Selectin / metabolism
  • Probability
  • Proto-Oncogene Protein c-ets-1 / pharmacology*
  • RNA, Messenger / analysis
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • Reference Values
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription Factors / analysis
  • Transcription Factors / metabolism*
  • Tunica Intima / drug effects
  • Tunica Intima / pathology

Substances

  • Biomarkers
  • Chemokine CCL2
  • Cytokines
  • E-Selectin
  • P-Selectin
  • Proto-Oncogene Protein c-ets-1
  • RNA, Messenger
  • Transcription Factors