Novel aspects on signal-transduction in the pancreatic beta-cell

Nutr Metab Cardiovasc Dis. 2006 Mar:16 Suppl 1:S7-10. doi: 10.1016/j.numecd.2005.11.005. Epub 2006 Feb 9.

Abstract

The glucose-stimulus/insulin-secretion-coupling by the pancreatic beta-cell, which guarantees the maintenance of glucose homeostasis in man, is regulated by a sophisticated interplay between glucose and a plethora of additional factors. Besides other nutrients, incretins, nerval innervation, systemic growth factors as well as autocrine and paracrine regulatory loops within the islet of Langerhans modulate the function of the insulin-producing beta-cell. Although the modulatory role of these factors is well appreciated, the underlying molecular mechanisms involved remain poorly understood. However, in most cases beta-cell membrane receptors coupled primarily to either G-proteins or tyrosine kinases, which subsequently activate respective second messenger cascades, are involved. In the present mini-review we will discuss the role of signaling through some of these receptor-operated effector systems in the light of pancreatic beta-cell signal-transduction.

Publication types

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

MeSH terms

  • Diabetes Mellitus / metabolism*
  • GTP-Binding Proteins / metabolism
  • Glucose / metabolism*
  • Humans
  • Inositol Phosphates / metabolism
  • Insulin / metabolism*
  • Insulin Secretion
  • Insulin-Secreting Cells / metabolism
  • Insulin-Secreting Cells / physiology*
  • Islets of Langerhans / metabolism*
  • Protein-Tyrosine Kinases / metabolism
  • Receptor, Insulin / metabolism*
  • Receptors, Cell Surface / metabolism
  • Signal Transduction

Substances

  • Inositol Phosphates
  • Insulin
  • Receptors, Cell Surface
  • Protein-Tyrosine Kinases
  • Receptor, Insulin
  • GTP-Binding Proteins
  • Glucose