Crosstalk between cyclophilins and T lymphocytes in coronary artery disease

Exp Cell Res. 2021 Mar 15;400(2):112514. doi: 10.1016/j.yexcr.2021.112514. Epub 2021 Feb 11.

Abstract

Cardiovascular diseases and atherosclerosis are currently some of the most widespread diseases of our time. Within cardiovascular disease, coronary artery disease and underlying atherosclerosis were recently linked with systemic and local inflammation. Cyclophilins participate in the initiation and progression of these inflammatory-related diseases. Cyclophilins are released into the extracellular space upon inflammatory stimuli and participate in the pathology of cardiovascular diseases. The cell surface receptor for extracellular cyclophilins, the CD147 receptor, also contributes to coronary artery disease pathogenesis. Nevertheless, the physiological relevance of cyclophilin's family and their receptor in cardiovascular diseases remains unclear. The present study aimed to better understand the role of cyclophilins in cardiovascular artery disease and their relationship with inflammation. Hence, cyclophilins and pro-inflammatory interleukins were measured in the serum of 30 subjects (divided into three groups according to coronary artery disease status: 10 patients with acute coronary syndrome, 10 patients with chronic coronary artery disease, and 10 control volunteers). In addition, cyclophilin levels and CD147 receptor expression were measured in T lymphocytes purified from these subjects. Cyclophilin A, B, and C, pro-inflammatory interleukins, and CD147 membrane expression were significantly elevated in patients with coronary artery disease.

Keywords: Atherosclerosis; CD147 receptor; Coronary artery disease; Cyclophilins; Inflammation; T lymphocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Basigin / metabolism*
  • Case-Control Studies
  • Cell Communication*
  • Coronary Artery Disease / immunology
  • Coronary Artery Disease / metabolism
  • Coronary Artery Disease / pathology*
  • Cyclophilins / metabolism*
  • Female
  • Humans
  • Interleukins / metabolism*
  • Male
  • Middle Aged
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism

Substances

  • BSG protein, human
  • Interleukins
  • Basigin
  • Cyclophilins