Protein disregulation in red blood cell membranes of type 2 diabetic patients

Biochem Biophys Res Commun. 2003 Sep 12;309(1):196-200. doi: 10.1016/s0006-291x(03)01559-6.

Abstract

The proteomics analysis was used to search for the membrane proteins related to the type 2 diabetes in human red blood cell (RBC). To improve the solubilization and separation for membrane proteins during two-dimensional electrophoresis (2-DE), several types of chaotropes and surfactants were tested. The optimized condition was then screened. About 1000 protein spots from RBC membranes can be resolved on the 2-D gel. To compare the 2-DE patterns between RBC membranes of type 2 diabetic patients and healthy controls, a total of 42 proteins that were differentially expressed were found. The analysis shows that flotillin-1, a recently discovered membrane protein of RBC lipid rafts, appears to be affected in the disease. The result would be quite interesting because flotillin-1 in adipocytes functions is related to stimulate activation of glucose transporter 4 in response to insulin. Additionally, syntaxin 1C and arginase were also disregulated in patient RBC membranes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Antigens, Surface / metabolism
  • Arginase / metabolism
  • Blotting, Western
  • Cell Membrane / metabolism*
  • Diabetes Mellitus, Type 2 / blood*
  • Electrophoresis, Gel, Two-Dimensional
  • Erythrocytes / metabolism*
  • Gene Expression Regulation*
  • Humans
  • Image Processing, Computer-Assisted
  • Insulin / metabolism
  • Lipid Metabolism
  • Membrane Microdomains / metabolism
  • Membrane Proteins / chemistry
  • Middle Aged
  • Monosaccharide Transport Proteins / metabolism
  • Nerve Tissue Proteins / metabolism
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • Surface-Active Agents / chemistry
  • Syntaxin 1
  • Time Factors

Substances

  • Antigens, Surface
  • Insulin
  • Membrane Proteins
  • Monosaccharide Transport Proteins
  • Nerve Tissue Proteins
  • STX1A protein, human
  • Surface-Active Agents
  • Syntaxin 1
  • flotillins
  • Arginase