Impact of Enhanced Phagocytosis of Glycated Erythrocytes on Human Endothelial Cell Functions
Chloé Turpin,
Marie Laurine Apalama,
Bastian Carnero,
Alberto Otero-Cacho,
Alberto P. Munuzuri,
Maria Teresa Flores-Arias,
Erick Vélia,
Olivier Meilhac,
Emmanuel Bourdon,
Ezequiel Álvarez,
Philippe Rondeau
Affiliations
Chloé Turpin
UMR 1188 Diabète Athérothombose Thérapies Réunion Océan Indien (DéTROI), INSERM, Université de La Réunion, 97400 Saint-Denis, France
Marie Laurine Apalama
UMR 1188 Diabète Athérothombose Thérapies Réunion Océan Indien (DéTROI), INSERM, Université de La Réunion, 97400 Saint-Denis, France
Bastian Carnero
Photonics4Life Research Group, Applied Physics Department, Faculty of Physics, Institute of Materials (iMATUS), Universidade de Santiago de Compostela, 15782 Santiago de Compostela, Spain
Alberto Otero-Cacho
Galician Center for Mathematical Research and Technology (CITMAga) and Group of Nonlinear Physics, Department of Physics, Universidade de Santiago de Compostela, 15782 Santiago de Compostela, Spain
Alberto P. Munuzuri
Galician Center for Mathematical Research and Technology (CITMAga) and Group of Nonlinear Physics, Department of Physics, Universidade de Santiago de Compostela, 15782 Santiago de Compostela, Spain
Maria Teresa Flores-Arias
Photonics4Life Research Group, Applied Physics Department, Faculty of Physics, Institute of Materials (iMATUS), Universidade de Santiago de Compostela, 15782 Santiago de Compostela, Spain
Erick Vélia
Clinique Sainte-Clotilde, Groupe Clinifutur, Pôle Mère Enfant, 97490 Sainte-Clotilde, France
Olivier Meilhac
UMR 1188 Diabète Athérothombose Thérapies Réunion Océan Indien (DéTROI), INSERM, Université de La Réunion, 97400 Saint-Denis, France
Emmanuel Bourdon
UMR 1188 Diabète Athérothombose Thérapies Réunion Océan Indien (DéTROI), INSERM, Université de La Réunion, 97400 Saint-Denis, France
Ezequiel Álvarez
Cardiology Group, Health Research Institute of Santiago de Compostela (IDIS), Hospital Universitario de Santiago de Compostela (SERGAS), Trav. Choupana s/n, 15706 Santiago de Compostela, Spain
Philippe Rondeau
UMR 1188 Diabète Athérothombose Thérapies Réunion Océan Indien (DéTROI), INSERM, Université de La Réunion, 97400 Saint-Denis, France
Diabetes is associated with a high mortality rate due to vascular complications. Chronic hyperglycemia in diabetes leads to enhanced oxidative stress and glycation. Here, we explored the impact of glycation on human erythrocyte characteristics and capacity to affect endothelial cell function following erythrophagocytosis. Native and glucose-mediated glycated erythrocytes were prepared and characterized in terms of structural and deformability modifications. Erythrocyte preparations were tested for their binding and phagocytosis capacity as well as the potential functional consequences on human endothelial cell lines and primary cultures. Oxidative modifications were found to be enhanced in glycated erythrocytes after determination of their deformability, advanced glycation end-product content and eryptosis. Erythrophagocytosis by endothelial cells was significantly increased when incubated in the presence of glycated erythrocytes. In addition, higher iron accumulation, oxidative stress and impaired endothelial cell permeability were evidenced in cells previously incubated with glycated erythrocytes. When cultured under flow conditions, cellular integrity was disrupted by glycated erythrocytes at microvessel bifurcations, areas particularly prone to vascular complications. This study provides important new data on the impact of glycation on the structure of erythrocytes and their ability to alter endothelial cell function. Increased erythrophagocytosis may have a deleterious impact on endothelial cell function with adverse consequences on diabetic vascular complications.