Insulin receptors and downstream substrates associate with membrane microdomains after treatment with insulin or chromium(III) picolinate

Cell Biochem Biophys. 2012 Apr;62(3):441-50. doi: 10.1007/s12013-011-9326-x.


We have examined the association of insulin receptors (IR) and downstream signaling molecules with membrane microdomains in rat basophilic leukemia (RBL-2H3) cells following treatment with insulin or tris(2-pyridinecarbxylato)chromium(III) (Cr(pic)(3)). Single-particle tracking demonstrated that individual IR on these cells exhibited reduced lateral diffusion and increased confinement within 100 nm-scale membrane compartments after treatment with either 200 nM insulin or 10 μM Cr(pic)(3). These treatments also increased the association of native IR, phosphorylated insulin receptor substrate 1 and phosphorylated AKT with detergent-resistant membrane microdomains of characteristically high buoyancy. Confocal fluorescence microscopic imaging of Di-4-ANEPPDHQ labeled RBL-2H3 cells also showed that plasma membrane lipid order decreased following treatment with Cr(pic)(3) but was not altered by insulin treatment. Fluorescence correlation spectroscopy demonstrated that Cr(pic)(3) did not affect IR cell-surface density or compete with insulin for available binding sites. Finally, Fourier transform infrared spectroscopy indicated that Cr(pic)(3) likely associates with the lipid interface in reverse-micelle model membranes. Taken together, these results suggest that activation of IR signaling in a cellular model system by both insulin and Cr(pic)(3) involves retention of IR in specialized nanometer-scale membrane microdomains but that the insulin-like effects of Cr(pic)(3) are due to changes in membrane lipid order rather than to direct interactions with IR.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cell Line
  • Detergents / chemistry
  • Hypoglycemic Agents / pharmacology
  • Insulin / pharmacology*
  • Iron Chelating Agents / pharmacology
  • Membrane Microdomains / drug effects
  • Membrane Microdomains / metabolism*
  • Phosphorylation
  • Picolinic Acids / pharmacology*
  • Protein Binding
  • Pyridinium Compounds / chemistry
  • Rats
  • Receptor, Insulin / metabolism*
  • Substrate Specificity


  • Detergents
  • Hypoglycemic Agents
  • Insulin
  • Iron Chelating Agents
  • Picolinic Acids
  • Pyridinium Compounds
  • di-4-ANEPPDHQ
  • Receptor, Insulin
  • picolinic acid