Activation of G proteins by GIV-GEF is a pivot point for insulin resistance and sensitivity

Mol Biol Cell. 2015 Nov 15;26(23):4209-23. doi: 10.1091/mbc.E15-08-0553. Epub 2015 Sep 16.

Abstract

Insulin resistance (IR) is a metabolic disorder characterized by impaired insulin signaling and cellular glucose uptake. The current paradigm for insulin signaling centers upon the insulin receptor (InsR) and its substrate IRS1; the latter is believed to be the sole conduit for postreceptor signaling. Here we challenge that paradigm and show that GIV/Girdin, a guanidine exchange factor (GEF) for the trimeric G protein Gαi, is another major hierarchical conduit for the metabolic insulin response. By virtue of its ability to directly bind InsR, IRS1, and phosphoinositide 3-kinase, GIV serves as a key hub in the immediate postreceptor level, which coordinately enhances the metabolic insulin response and glucose uptake in myotubes via its GEF function. Site-directed mutagenesis or phosphoinhibition of GIV-GEF by the fatty acid/protein kinase C-theta pathway triggers IR. Insulin sensitizers reverse phosphoinhibition of GIV and reinstate insulin sensitivity. We also provide evidence for such reversible regulation of GIV-GEF in skeletal muscles from patients with IR. Thus GIV is an essential upstream component that couples InsR to G-protein signaling to enhance the metabolic insulin response, and impairment of such coupling triggers IR. We also provide evidence that GIV-GEF serves as therapeutic target for exogenous manipulation of physiological insulin response and reversal of IR in skeletal muscles.

Publication types

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

MeSH terms

  • Cells, Cultured
  • Fatty Acids / metabolism
  • Female
  • GTP-Binding Protein Regulators / metabolism*
  • GTP-Binding Protein alpha Subunits, Gi-Go / metabolism*
  • Guanine Nucleotide Exchange Factors / metabolism*
  • Humans
  • Insulin / metabolism
  • Insulin Receptor Substrate Proteins / metabolism
  • Insulin Resistance / physiology*
  • Microfilament Proteins / metabolism*
  • Muscle, Skeletal / metabolism
  • Phosphatidylinositol 3-Kinase / metabolism
  • Phosphorylation
  • Protein-Tyrosine Kinases / metabolism
  • Receptor, Insulin / metabolism
  • Signal Transduction
  • Vesicular Transport Proteins / metabolism*

Substances

  • CCDC88A protein, human
  • Fatty Acids
  • GTP-Binding Protein Regulators
  • Guanine Nucleotide Exchange Factors
  • IRS1 protein, human
  • Insulin
  • Insulin Receptor Substrate Proteins
  • Microfilament Proteins
  • Vesicular Transport Proteins
  • Phosphatidylinositol 3-Kinase
  • Protein-Tyrosine Kinases
  • Receptor, Insulin
  • GTP-Binding Protein alpha Subunits, Gi-Go