Coronary atherosclerosis is associated with macrophage polarization in epicardial adipose tissue

J Am Coll Cardiol. 2011 Jul 12;58(3):248-55. doi: 10.1016/j.jacc.2011.01.048.

Abstract

Objectives: The purpose of this report was to assess the link between macrophage polarization in epicardial adipose tissue and atherosclerosis in patients with coronary artery disease (CAD).

Background: Macrophage accumulation enhances chronic inflammation in adipose tissue, but macrophage phenotypic change in human epicardial adipose tissue and its role in atherogenesis are unknown.

Methods: Samples were obtained from epicardial and subcutaneous adipose tissue during elective cardiac surgery (CAD, n = 38; non-CAD, n = 40). Infiltration of M1/M2 macrophages was investigated by immunohistochemical staining with antibodies against CD11c and CD206, respectively. Expression of pro- and anti-inflammatory adipocytokines in adipose tissue was evaluated by real-time quantitative polymerase chain reaction.

Results: Infiltration of macrophages and expression of pro- and anti-inflammatory cytokines were enhanced in epicardial fat of patients with CAD compared with that in non-CAD patients (p < 0.05). The ratio of M1/M2 macrophages was positively correlated with the severity of CAD (r = 0.312, p = 0.039). Furthermore, the expression of pro-inflammatory cytokines was positively correlated, and the expression of anti-inflammatory cytokines was negatively correlated with the ratio of M1/M2 macrophages in epicardial adipose tissue of CAD patients. By contrast, there was no significant difference in macrophage infiltration and cytokine expression in subcutaneous adipose tissue between the CAD and non-CAD groups.

Conclusions: The ratio of M1/M2 macrophages in epicardial adipose tissue of CAD patients is changed compared with that in non-CAD patients. Human coronary atherosclerosis is associated with macrophage polarization in epicardial adipose tissue.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / pathology*
  • Aged
  • Antigens, CD / analysis
  • Antigens, Differentiation, Myelomonocytic / analysis
  • CD11c Antigen / analysis
  • Chemokine CCL2 / metabolism
  • Coronary Artery Disease / pathology*
  • Cytokines / metabolism
  • Female
  • Humans
  • Immunohistochemistry
  • Inflammation / pathology
  • Interleukin-6 / metabolism
  • Lectins, C-Type / analysis
  • Macrophages / metabolism
  • Macrophages / pathology*
  • Male
  • Mannose Receptor
  • Mannose-Binding Lectins / analysis
  • Pericardium / pathology*
  • Receptors, Cell Surface / analysis
  • Subcutaneous Fat / pathology

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • CD11c Antigen
  • CD68 antigen, human
  • Chemokine CCL2
  • Cytokines
  • Interleukin-6
  • Lectins, C-Type
  • Mannose Receptor
  • Mannose-Binding Lectins
  • Receptors, Cell Surface