Enhanced oxidative stress and damage in glycated erythrocytes

PLoS One. 2020 Jul 6;15(7):e0235335. doi: 10.1371/journal.pone.0235335. eCollection 2020.

Abstract

Diabetes is associated with a dramatic mortality rate due to its vascular complications. Chronic hyperglycemia in diabetes leads to enhanced glycation of erythrocytes and oxidative stress. Even though erythrocytes play a determining role in vascular complications, very little is known about how erythrocyte structure and functionality can be affected by glycation. Our objective was to decipher the impact of glycation on erythrocyte structure, oxidative stress parameters and capacity to interact with cultured human endothelial cells. In vitro glycated erythrocytes were prepared following incubation in the presence of different concentrations of glucose. To get insight into the in vivo relevance of our results, we compared these data to those obtained using red blood cells purified from diabetics or non-diabetics. We measured erythrocyte deformability, susceptibility to hemolysis, reactive oxygen species production and oxidative damage accumulation. Altered structures, redox status and oxidative modifications were increased in glycated erythrocytes. These modifications were associated with reduced antioxidant defence mediated by enzymatic activity. Enhanced erythrocyte phagocytosis by endothelial cells was observed when cultured with glycated erythrocytes, which was associated with increased levels of phosphatidylserine-likely as a result of an eryptosis phenomenon triggered by the hyperglycemic treatment. Most types of oxidative damage identified in in vitro glycated erythrocytes were also observed in red blood cells isolated from diabetics. These results bring new insights into the impact of glycation on erythrocyte structure, oxidative damage and their capacity to interact with endothelial cells, with a possible relevance to diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blood Glucose / metabolism
  • Cell Line
  • Coculture Techniques
  • Diabetes Mellitus, Type 2 / blood*
  • Diabetes Mellitus, Type 2 / pathology
  • Endothelial Cells
  • Eryptosis
  • Erythrocyte Deformability
  • Erythrocytes / metabolism
  • Erythrocytes / pathology*
  • Glycated Hemoglobin / analysis
  • Glycation End Products, Advanced / metabolism*
  • Healthy Volunteers
  • Hemolysis
  • Humans
  • Oxidative Stress
  • Primary Cell Culture
  • Reactive Oxygen Species / metabolism*

Substances

  • Blood Glucose
  • Glycated Hemoglobin A
  • Glycation End Products, Advanced
  • Reactive Oxygen Species
  • hemoglobin A1c protein, human

Grants and funding

This work was supported by the Ministère de l'Enseignement Supérieur et de la Recherche, the Université de La Réunion, the "Structure fédérative de recherche biosécurité en milieu tropical (BIOST) and by the European Regional Development Funds RE0001897 (EU- Région Réunion -French State national counterpart)."