Depletion interaction forces contribute to erythrocyte-endothelial adhesion in diabetes

Biochem Biophys Res Commun. 2019 Aug 13;516(1):144-148. doi: 10.1016/j.bbrc.2019.06.018. Epub 2019 Jun 11.

Abstract

Abnormal adhesion of red blood cells (RBC) to the endothelium has been linked to the pathophysiology of several diseases associated with vascular disorders. Various biochemical changes on the outer membrane of RBC, as well as plasma protein levels, have been identified as possibly playing key roles, but the detailed interplay between plasma factors and cellular factors often remains unclear. In this work, we identified an alternative pathway by demonstrating that non-adsorbing macromolecules can also have a marked impact on the adhesion efficiency of RBC from patients with type 2 Diabetes (T2DM) to endothelial cells (EC). RBC isolated from blood samples of T2DM patients were suspended in isotonic solutions of dextran in order to mimic the impact of non-adsorbing macromolecules. Static and continuous flow adhesion assays were used to determine the adhesion behavior of T2DM RBC with EC and the results compared with those of normal controls. We found that the presence of non-adsorbing molecules promotes an increase in T2DM RBC - EC adhesion and that these RBC exhibit much greater adhesion than normal red cells. Our results thus suggest that the depletion mechanism might be an alternative phenomenon through which plasma proteins could cause enhanced RBC-EC adhesion in diabetes mellitus. These findings contribute towards the comprehensive understanding of pathophysiological mechanisms of vascular complications in diabetes and other diseases with similar vascular sequelae.

Keywords: Cell adhesion; Dextran; Nonreactive polymers; Red blood cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cell Adhesion
  • Cell Communication
  • Diabetes Mellitus, Type 2 / pathology*
  • Endothelial Cells / cytology
  • Endothelial Cells / pathology*
  • Erythrocytes / cytology
  • Erythrocytes / pathology*
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • Middle Aged