Expression of adhesion molecules on granulocytes and monocytes following myocardial infarction in rats drinking white wine

PLoS One. 2018 May 10;13(5):e0196842. doi: 10.1371/journal.pone.0196842. eCollection 2018.

Abstract

Neutrophils and monocytes through their CD15s, CD11b and CD44 adhesion molecules are implicated in the initiation and resolution of cardiac inflammation as well as in healing processes after the myocardial infarction (MI). The aim of this study was to determine the effect of white wine consumption on granulocyte and monocyte CD15s, CD11b, and CD44 expression 24h after the surgically inflicted MI. Granulocytes and monocytes were analyzed by flow cytometry, using whole blood of male Sprague-Dawley rats that consumed white wine for 4 weeks. This group was compared with water only drinking controls, sham animals (subject to surgery without myocardial infarction) and baseline group (intact animals that received no intervention prior to being sacrificed). Sham animals did not differ from baseline animals in CD11b+CD44+ percentage and CD44+ median fluorescence intensity. Wine drinking was associated with striking increase in CD44 expression on monocyte subpopulations. Its expression was three and fourfold increased on monocytes and large monocytes, respectively, relative to the water only drinking controls. Because of known role of CD44 on suppression of post-infarction inflammation, its upregulation on granulocytes and monocytes may significantly contribute to the microenvironment favourable for the cardiac regeneration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohol Drinking / metabolism*
  • Animals
  • CD11b Antigen / metabolism
  • Cell Adhesion Molecules / metabolism*
  • Cellular Microenvironment / physiology
  • Granulocytes / metabolism*
  • Heart / physiology
  • Hyaluronan Receptors / metabolism
  • Inflammation / metabolism
  • Leukocyte Count / methods
  • Lewis X Antigen / metabolism
  • Male
  • Monocytes / metabolism*
  • Myocardial Infarction / metabolism*
  • Neutrophils / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Up-Regulation / physiology
  • Wine

Substances

  • CD11b Antigen
  • Cell Adhesion Molecules
  • Hyaluronan Receptors
  • Lewis X Antigen

Associated data

  • figshare/ac7456ab00c89750f38b

Grants and funding

This study was performed under the framework of the research project “Biological effects of wine: the influence of vinification technology, dealcoholisation and aging of wine” (No. 8652, PI Mladen Boban) supported by the Croatian Science Foundation.