Monocyte chemoattractant protein-1 or macrophage inflammatory protein-1alpha deficiency does not affect angiotensin II-induced intimal hyperplasia in carotid artery ligation model

Cardiovasc Pathol. 2007 Jul-Aug;16(4):231-6. doi: 10.1016/j.carpath.2007.01.006. Epub 2007 Mar 21.

Abstract

Background: Angiotensin II (Ang II) promotes atherosclerotic vascular diseases, in which proinflammatory and proliferative effects play a major pathogenic role. Ang II up-regulates chemokines, such as monocyte chemoattractant protein (MCP)-1 and macrophage inflammatory protein (MIP)-1alpha, which are important pro-inflammatory factors mediating infiltration of inflammatory cells into atherosclerotic lesion. The aim of the present study was to determine whether the presence of MCP-1 or MIP-1alpha is essential in Ang II-induced intimal hyperplasia in the carotid artery ligation model.

Methods: Six-month-old male C57BL/6-, MCP-1-, or MIP-1alpha-deficient mice underwent ligation of the common left carotid artery and were randomly assigned to receive either vehicle or Ang II (1.4 mg kg(-1) day(-1)) via a subcutaneously implanted osmotic infusion pump (model 2004, Alzet) for 4 weeks.

Results: Ang II not only increased MCP-1 and MIP-1alpha production but also enhanced neo-intimal formation, media thickness, and adventitia development in the ligated carotid arteries in C57BL/6 mice. However, MCP-1 or MIP-1alpha deficiency failed to affect intimal hyperplasia in vascular remodeling.

Conclusion: These results indicate that MCP-1 or MIP-1alpha may not be essential in mediating the proliferative effects of Ang II, a major pathological changes in intimal hyperplasia in the carotid artery ligation model.

MeSH terms

  • Angiotensin II / metabolism*
  • Animals
  • Carotid Arteries / metabolism*
  • Carotid Arteries / pathology
  • Carotid Artery Injuries / metabolism
  • Carotid Artery Injuries / pathology
  • Chemokine CCL2 / metabolism*
  • Chemokine CCL3
  • Chemokine CCL4
  • Hyperplasia
  • Immunohistochemistry
  • Ligation
  • Macrophage Inflammatory Proteins / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Tunica Intima / metabolism
  • Tunica Intima / pathology*

Substances

  • Ccl2 protein, mouse
  • Chemokine CCL2
  • Chemokine CCL3
  • Chemokine CCL4
  • Macrophage Inflammatory Proteins
  • Angiotensin II