A C-peptide complex with albumin and Zn2+ increases measurable GLUT1 levels in membranes of human red blood cells

Sci Rep. 2020 Oct 15;10(1):17493. doi: 10.1038/s41598-020-74527-6.

Abstract

People with type 1 diabetes (T1D) require exogenous administration of insulin, which stimulates the translocation of the GLUT4 glucose transporter to cell membranes. However, most bloodstream cells contain GLUT1 and are not directly affected by insulin. Here, we report that C-peptide, the 31-amino acid peptide secreted in equal amounts with insulin in vivo, is part of a 3-component complex that affects red blood cell (RBC) membranes. Multiple techniques were used to demonstrate saturable and specific C-peptide binding to RBCs when delivered as part of a complex with albumin. Importantly, when the complex also included Zn2+, a significant increase in cell membrane GLUT1 was measured, thus providing a cellular effect similar to insulin, but on a transporter on which insulin has no effect.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adenosine Triphosphate / chemistry
  • Animals
  • Biological Transport
  • C-Peptide / administration & dosage*
  • Cattle
  • Cell Membrane / metabolism
  • Diabetes Mellitus, Type 1 / metabolism
  • Erythrocytes / metabolism*
  • Gene Expression Regulation
  • Glucose / metabolism
  • Glucose Transporter Type 1 / metabolism*
  • Humans
  • Insulin / metabolism
  • Serum Albumin, Bovine / chemistry*
  • Zinc / administration & dosage*

Substances

  • C-Peptide
  • Glucose Transporter Type 1
  • Insulin
  • SLC2A1 protein, human
  • Serum Albumin, Bovine
  • Adenosine Triphosphate
  • Glucose
  • Zinc