Increased retinol-free RBP4 contributes to insulin resistance in gestational diabetes mellitus

Arch Gynecol Obstet. 2017 Jul;296(1):53-61. doi: 10.1007/s00404-017-4378-9. Epub 2017 May 20.

Abstract

Purpose: Retinol-binding protein 4 (RBP4) is a circulating retinol transporter that is strongly associated with insulin resistance. The aim of this study was to evaluate the RBP4 and retinol level in rat model of gestational diabetes mellitus and the relationship between retinol-free RBP4 (apo-RBP4), retinol-bound RBP4 (holo-RBP4) and insulin resistance.

Methods: Pregnant rats were administered streptozotocin to induce diabetes. The RBP4 and retinol levels were evaluated in GDM and normal pregnant rats. After then, normal pregnant rats were divided into two groups to receive either apo-RBP4 or vehicle injection. The metabolic parameters and insulin signaling in adipose tissue, skeletal muscle and liver were determined in apo-RBP4 and control groups. Primary human adipocytes were cultured in vitro with different proportions of apo-RBP4 and holo-RBP4 for 24 h. The interaction between RBP4 and STRA6 was assessed by co-immunoprecipitation, and the expression of JAK-STAT pathway and insulin signaling were detected by Western blotting and immunofluorescence.

Results: We found increases in serum RBP4 levels and the RBP4:retinol ratio but not in the retinol levels in GDM rats. Exogenous apo-RBP4 injection attenuated insulin sensitivity in pregnant rats. In vitro, a prolonged interaction between RBP4 and STRA6 was observed when apo-RBP4 was present. In response to increased apo-RBP4 levels, cells showed elevated activation of the JAK2/STAT5 cascade and SOCS3 expression, decreased phosphorylation of IR and IRS1, and attenuated GLUT4 translocation and glucose uptake upon insulin stimulation.

Conclusion: Apo-RBP4 is a ligand that activates the STRA6 signaling cascade, inducing insulin resistance in GDM.

Keywords: Apo-RBP4; Gestational diabetes mellitus; Insulin resistance; Retinol-binding protein 4.

MeSH terms

  • Adipocytes / metabolism
  • Adipose Tissue / metabolism
  • Animals
  • Cells, Cultured
  • Diabetes, Gestational / chemically induced
  • Diabetes, Gestational / metabolism*
  • Female
  • Humans
  • Insulin / metabolism
  • Insulin Resistance*
  • Janus Kinase 2
  • Liver / metabolism
  • Membrane Proteins / metabolism
  • Muscle, Skeletal / metabolism
  • Pregnancy
  • Rats
  • Retinol-Binding Proteins, Plasma / metabolism
  • Retinol-Binding Proteins, Plasma / physiology*
  • Signal Transduction
  • Streptozocin
  • Vitamin A / blood*

Substances

  • Insulin
  • Membrane Proteins
  • Rbp4 protein, rat
  • Retinol-Binding Proteins, Plasma
  • STRA6 protein, rat
  • Vitamin A
  • Streptozocin
  • JAK2 protein, human
  • Janus Kinase 2