Endothelial microparticles exert differential effects on functions of Th1 in patients with acute coronary syndrome

Int J Cardiol. 2013 Oct 15;168(6):5396-404. doi: 10.1016/j.ijcard.2013.08.050. Epub 2013 Aug 24.

Abstract

Background: Endothelial microparticles (EMPs) can be involved in inflammatory process, blood coagulation, and regulation of vascular function. However, it remains unclear whether EMPs participate in the pathogenesis of ACS. The purpose of this study is to investigate the impact of EMPs on Th1/Th2 development and functions in vitro.

Methods: Eight-five patients were allocated into SAP group (n=27), UAP group (n=28), and AMI group (n=30). Twenty hospitalized patients with normal coronary angiography were recruited as controls. The frequency of EMPs, IFN-γ, and IL-4 levels were measured, and the correlation between EMPs and Th1/Th2 cytokine was analyzed. PBMCs isolated from patients with ACS were treated in vitro with EMPs. This was followed by flow cytometry for Th1/Th2 counts, real-time PCR and western blotting for T-bet and GATA mRNA and protein expression, and ELISA for IFN-γ, TNF-α, IL-4, and IL-10.

Results: This study proved that the frequency of EMPs was significantly increased in ACS patients. There was a significant positive correlation between EMPs and IFN-γ. EMPs could significantly upregulate the differentiation and function of Th1 through increasing the expression of T-bet mRNA and protein. Furthermore, this study also indicated that EMP treatment in vitro could promote the expression of TNF-α, which exerts adverse effects on the pathogenesis and progression of atherosclerosis.

Conclusions: EMPs may be involved in the immune and inflammatory processes that take part in artery atherosclerosis and that they do so by regulating Th1/Th2 differentiation and function. They may play an important role in the pathogenesis of coronary atherosclerosis and plaque instability.

Keywords: Acute coronary syndrome; Endothelial microparicles; Helper T cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Coronary Syndrome / immunology*
  • Acute Coronary Syndrome / metabolism*
  • Acute Coronary Syndrome / pathology
  • Aged
  • Angina, Stable / immunology*
  • Angina, Stable / metabolism*
  • Angina, Stable / pathology
  • Atherosclerosis / immunology
  • Atherosclerosis / metabolism
  • Atherosclerosis / pathology
  • Cell-Derived Microparticles / immunology
  • Cell-Derived Microparticles / metabolism
  • Cell-Derived Microparticles / pathology
  • Cells, Cultured
  • Endothelium, Vascular / immunology
  • Endothelium, Vascular / metabolism
  • Endothelium, Vascular / pathology
  • Female
  • GATA3 Transcription Factor / genetics
  • GATA3 Transcription Factor / metabolism
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • Interferon-gamma / blood
  • Interleukin-4 / blood
  • Male
  • Middle Aged
  • T-Box Domain Proteins / genetics
  • T-Box Domain Proteins / metabolism
  • Th1 Cells / cytology
  • Th1 Cells / immunology*
  • Th1 Cells / metabolism*
  • Th2 Cells / cytology
  • Th2 Cells / immunology
  • Th2 Cells / metabolism

Substances

  • GATA3 Transcription Factor
  • IL4 protein, human
  • T-Box Domain Proteins
  • T-box transcription factor TBX21
  • Interleukin-4
  • Interferon-gamma