Glucose and GTP-binding protein-coupled receptor cooperatively regulate transient receptor potential-channels to stimulate insulin secretion [Review]

Endocr J. 2016 Oct 29;63(10):867-876. doi: 10.1507/endocrj.EJ16-0262. Epub 2016 Jul 17.

Abstract

In pancreatic β-cells, glucose-induced closure of the ATP-sensitive K+ (KATP) channel is an initial process triggering glucose-stimulated insulin secretion (GSIS). This KATP-channel dependent pathway has been believed to be a central mechanism for GSIS. However, since the resting membrane potential of cells is determined by the balance of the net result of current amplitudes in outward and inward directions, it must be taken into consideration that not only KATP channel inhibition but also inward current via the basal opening of non-selective cation channels (NSCCs) plays a crucial role in membrane potential regulation. The basal activity of NSCCs is essential to effectively evoke depolarization in concert with KATP channel closure that is dependent on glucose metabolism. The present study summarizes recent findings regarding the roles of NSCCs in GSIS and GTP-binding protein coupled receptor-(GPCR) operated potentiation of GSIS.

Publication types

  • Review

MeSH terms

  • Animals
  • GTP-Binding Proteins / metabolism
  • GTP-Binding Proteins / physiology*
  • Glucose / metabolism
  • Glucose / physiology*
  • Humans
  • Insulin / metabolism*
  • Insulin Secretion
  • Insulin-Secreting Cells / metabolism
  • Receptors, G-Protein-Coupled / physiology*
  • Signal Transduction
  • Transient Receptor Potential Channels / metabolism*
  • Transient Receptor Potential Channels / physiology

Substances

  • Insulin
  • Receptors, G-Protein-Coupled
  • Transient Receptor Potential Channels
  • GTP-Binding Proteins
  • Glucose