The neuropeptide PACAP promotes the alpha-secretase pathway for processing the Alzheimer amyloid precursor protein

FASEB J. 2006 Mar;20(3):512-4. doi: 10.1096/fj.05-4812fje. Epub 2006 Jan 9.

Abstract

The neuropeptide pituitary adenylate cyclase-activating polypeptide (PACAP) has neurotrophic as well as anti-apoptotic properties and is involved in learning and memory processes. Its specific G protein-coupled receptor PAC1 is expressed in several central nervous system (CNS) regions, including the hippocampal formation. Here we examined the effect of PAC1 receptor activation on alpha-secretase cleavage of the amyloid precursor protein (APP) and the production of secreted APP (APPsalpha). Stimulation of endogenously expressed PAC1 receptors with PACAP in human neuroblastoma cells increased APPsalpha secretion, which was completely inhibited by the PAC1 receptor specific antagonist PACAP-(6-38). In HEK cells stably overexpressing functional PAC1 receptors, PACAP-27 and PACAP-38 strongly stimulated alpha-secretase cleavage of APP. The PACAP-induced APPsalpha production was dose dependent and saturable. This increase of alpha-secretase activity was completely abolished by hydroxamate-based metalloproteinase inhibitors, including a preferential ADAM 10 inhibitor. By using several specific protein kinase inhibitors, we show that the MAP-kinase pathway [including extracellular-regulated kinase (ERK) 1 and ERK2] and phosphatidylinositol 3-kinase mediate the PACAP-induced alpha-secretase activation. Our findings provide evidence for a role of the neuropeptide PACAP in stimulation of the nonamyloidogenic pathway, which might be related to its neuroprotective properties.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADAM Proteins / analysis
  • ADAM10 Protein
  • ADAM17 Protein
  • Adenylyl Cyclases / metabolism
  • Alzheimer Disease / metabolism
  • Amino Acid Sequence
  • Amyloid Precursor Protein Secretases
  • Amyloid beta-Protein Precursor / metabolism*
  • Androstadienes / pharmacology
  • Animals
  • Aspartic Acid Endopeptidases
  • Calcium / metabolism
  • Cell Line / drug effects
  • Cell Line / metabolism
  • Cell Line, Tumor / drug effects
  • Cell Line, Tumor / metabolism
  • Cyclic AMP Response Element-Binding Protein / metabolism
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Endopeptidases / metabolism
  • Enzyme Activation
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Humans
  • Kidney
  • Membrane Proteins / analysis
  • Molecular Sequence Data
  • Neuroblastoma / pathology
  • PC12 Cells / drug effects
  • PC12 Cells / metabolism
  • Phosphatidylinositol 3-Kinases / physiology
  • Phosphoinositide-3 Kinase Inhibitors
  • Phosphorylation
  • Pituitary Adenylate Cyclase-Activating Polypeptide / pharmacology*
  • Protein Kinase C / physiology
  • Protein Processing, Post-Translational*
  • Rats
  • Receptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type I / agonists
  • Receptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type I / physiology*
  • Recombinant Fusion Proteins / physiology
  • Transfection
  • Wortmannin

Substances

  • Amyloid beta-Protein Precursor
  • Androstadienes
  • CREB1 protein, human
  • Cyclic AMP Response Element-Binding Protein
  • Membrane Proteins
  • Phosphoinositide-3 Kinase Inhibitors
  • Pituitary Adenylate Cyclase-Activating Polypeptide
  • Receptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type I
  • Recombinant Fusion Proteins
  • Cyclic AMP-Dependent Protein Kinases
  • Protein Kinase C
  • Extracellular Signal-Regulated MAP Kinases
  • Amyloid Precursor Protein Secretases
  • Endopeptidases
  • Aspartic Acid Endopeptidases
  • BACE1 protein, human
  • ADAM Proteins
  • ADAM9 protein, human
  • ADAM10 Protein
  • ADAM10 protein, human
  • ADAM17 Protein
  • Adenylyl Cyclases
  • Calcium
  • Wortmannin