Altered RBC membrane lipidome: A possible etiopathogenic link for the microvascular impairment in Type 2 diabetes

J Diabetes Complications. 2021 Oct;35(10):107998. doi: 10.1016/j.jdiacomp.2021.107998. Epub 2021 Jul 28.

Abstract

Aims: Disturbances in red blood cells' (RBCs) membrane structure, that result in altered rheological properties, have been implicated in the pathogenesis of microvascular complications of diabetes mellitus(T2DM). However, the compositional alterations in RBCs membranes of T2DM patients have not been characterized in detail.

Methods: NMR-based lipidomic approach used for the global investigation of the lipidome of RBCs membrane in 20 newly diagnosed T2DM patients. Twenty healthy individuals served as controls.

Results: In the lipidomic analysis, the discrimination power among the two groups was of high significance. T2DM patients characterized by an increased content of cholesterol, total sphingolipids, sphingomyelin and glycolipids, and decreased total phospholipids, mainly due to phosphatidylethanolamine, total ether glycerolipids and plasmalogen-phospholipids, and higher cholesterol-to-phospholipids molecular ratio compared to controls. In T2DM, lipids were esterified with saturated rather than unsaturated fatty acids, an atherogenic pattern that may be involved in the impairment of membrane fluidity and rigidity.

Conclusions: NMR-based lipidomic analysis of RBCs can provide insights into molecular lipid features of membrane microenvironment that influence their vital function and rheological behavior in microvascular network in T2DM.Early identification of these disturbances, even before the onset of diabetes, could critically help to the development of novel preventative and curative therapies for reducing the risk of microvascular dysfunction.

Keywords: Deformability; Fluidity; Lipidomics; NMR; Red blood cell membrane; Type 2 diabetes.

MeSH terms

  • Cell Membrane / chemistry*
  • Cholesterol / chemistry
  • Diabetes Mellitus, Type 2* / complications
  • Erythrocytes / chemistry*
  • Humans
  • Lipidomics*
  • Phospholipids / chemistry

Substances

  • Phospholipids
  • Cholesterol