Lipid transport by TMEM24 at ER-plasma membrane contacts regulates pulsatile insulin secretion

Science. 2017 Feb 17;355(6326):eaah6171. doi: 10.1126/science.aah6171.

Abstract

Insulin is released by β cells in pulses regulated by calcium and phosphoinositide signaling. Here, we describe how transmembrane protein 24 (TMEM24) helps coordinate these signaling events. We showed that TMEM24 is an endoplasmic reticulum (ER)-anchored membrane protein whose reversible localization to ER-plasma membrane (PM) contacts is governed by phosphorylation and dephosphorylation in response to oscillations in cytosolic calcium. A lipid-binding module in TMEM24 transports the phosphatidylinositol 4,5-bisphosphate [PI(4,5)P2] precursor phosphatidylinositol between bilayers, allowing replenishment of PI(4,5)P2 hydrolyzed during signaling. In the absence of TMEM24, calcium oscillations are abolished, leading to a defect in triggered insulin release. Our findings implicate direct lipid transport between the ER and the PM in the control of insulin secretion, a process impaired in patients with type II diabetes.

Publication types

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

MeSH terms

  • Animals
  • Biological Transport
  • COS Cells
  • Calcium Signaling
  • Cell Membrane / metabolism
  • Chlorocebus aethiops
  • Endoplasmic Reticulum / metabolism*
  • Gene Knockout Techniques
  • HeLa Cells
  • Humans
  • Hydrolysis
  • Insulin / metabolism*
  • Insulin Secretion
  • Lipid Metabolism*
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Phosphatidylinositol 4,5-Diphosphate / metabolism*
  • Phosphorylation

Substances

  • C2CD2L protein, human
  • Insulin
  • Membrane Proteins
  • Phosphatidylinositol 4,5-Diphosphate