Roles of cADPR and NAADP in pancreatic cells

Acta Biochim Biophys Sin (Shanghai). 2012 Sep;44(9):719-29. doi: 10.1093/abbs/gms044. Epub 2012 Jun 7.

Abstract

Cyclic ADP-ribose (cADPR) and nicotinic acid adenine dinucleotide phosphate (NAADP) are Ca(2+)-mobilizing nucleotides that were discovered in the late 1980s. Two decades of investigations have built up a considerable understanding about these two molecules that are related because both are derived from pyridine nucleotides and known to be generated by CD38/ADP-ribosyl cyclases. cADPR has been shown to target the ryanodine receptors in the endoplasmic reticulum whereas NAADP stimulates the two-pore channels in the endo-lysosomes. Accumulating results indicate that cADPR and NAADP are second messenger molecules mediating Ca(2+) signaling activated by a wide range of agonists. This article reviews what is known about these two molecules, especially regarding their signaling roles in the pancreatic cells.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • ADP-ribosyl Cyclase 1 / metabolism
  • Animals
  • Calcium / metabolism*
  • Cyclic ADP-Ribose / metabolism
  • Cyclic ADP-Ribose / physiology*
  • Endoplasmic Reticulum / metabolism
  • Humans
  • Lysosomes / metabolism
  • Models, Biological
  • NADP / analogs & derivatives*
  • NADP / metabolism
  • NADP / physiology
  • Pancreas / cytology
  • Pancreas / metabolism*
  • Second Messenger Systems / physiology

Substances

  • Cyclic ADP-Ribose
  • NADP
  • NAADP
  • ADP-ribosyl Cyclase 1
  • Calcium