IRR is involved in glucose-induced endocytosis after insulin secretion

J Pharmacol Sci. 2019 Jul;140(3):300-304. doi: 10.1016/j.jphs.2019.07.002. Epub 2019 Jul 5.

Abstract

Endocytosis after insulin secretion plays a pivotal role in the regulation of insulin secretion in pancreatic β-cells. Our recent study suggested that EPI64, a GTPase activating protein for Rab27a, contributes to the regulation of glucose-induced endocytosis, which is mediated by the GDP-bound form of Rab27a. Here, we identified insulin receptor-related receptor (IRR) as an EPI64-interacting protein. Knockdown of IRR inhibited glucose-induced uptake of transferrin, a marker of endocytosis, translocation of the guanine-nucleotide-exchange factor ARNO to the plasma membrane, and generation of phosphatidylinositol 3,4,5-trisphosphate (PIP3). These results suggest that IRR functions upstream of PIP3 generation and controls endocytosis after insulin secretion.

Keywords: Diabetes; Endocytosis; Insulin.

MeSH terms

  • Animals
  • Biological Transport / physiology
  • Cell Membrane / metabolism
  • Endocytosis / physiology*
  • GTPase-Activating Proteins / metabolism
  • Glucose / metabolism*
  • Insulin / metabolism*
  • Insulin Secretion / physiology*
  • Insulin-Secreting Cells / metabolism
  • Mice
  • Receptor, Insulin / metabolism*
  • rab GTP-Binding Proteins / metabolism
  • rab27 GTP-Binding Proteins / metabolism

Substances

  • GTPase-Activating Proteins
  • Insulin
  • rab27 GTP-Binding Proteins
  • Receptor, Insulin
  • insulin receptor-related receptor
  • rab GTP-Binding Proteins
  • Glucose