A TAG1-APP signalling pathway through Fe65 negatively modulates neurogenesis

Nat Cell Biol. 2008 Mar;10(3):283-94. doi: 10.1038/ncb1690. Epub 2008 Feb 17.

Abstract

The release of amyloid precursor protein (APP) intracellular domain (AICD) may be triggered by extracellular cues through gamma-secretase-dependent cleavage. AICD binds to Fe65, which may have a role in AICD-dependent signalling; however, the functional ligand has not been characterized. In this study, we have identified TAG1 as a functional ligand of APP. We found that, through an extracellular interaction with APP, TAG1 increased AICD release and triggered Fe65-dependent activity in a gamma-secretase-dependent manner. TAG1, APP and Fe65 colocalized in the neural stem cell niche of the fetal ventricular zone. Neural precursor cells from TAG1-/-, APP-/- and TAG1-/-;APP-/- mice had aberrantly enhanced neurogenesis, which was significantly reversed in TAG1-/- mice by TAG1 or AICD but not by AICD mutated at the Fe65 binding site. Notably, TAG1 reduced normal neurogenesis in Fe65+/+ mice. Abnormally enhanced neurogenesis also occurred in Fe65-/- mice but could not be reversed by TAG1. These results describe a TAG1-APP signalling pathway that negatively modulates neurogenesis through Fe65.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid Precursor Protein Secretases / metabolism
  • Amyloid beta-Protein Precursor / metabolism*
  • Animals
  • CHO Cells
  • Cell Adhesion Molecules, Neuronal / metabolism*
  • Cell Adhesion Molecules, Neuronal / physiology*
  • Contactin 2
  • Cricetinae
  • Cricetulus
  • Gene Expression Regulation*
  • Mice
  • Mice, Transgenic
  • Models, Biological
  • Nerve Tissue Proteins / metabolism
  • Nerve Tissue Proteins / physiology*
  • Neurons / metabolism*
  • Nuclear Proteins / metabolism
  • Nuclear Proteins / physiology*
  • Signal Transduction*
  • Stem Cells / metabolism

Substances

  • Amyloid beta-Protein Precursor
  • Apbb1 protein, mouse
  • Cell Adhesion Molecules, Neuronal
  • Cntn2 protein, mouse
  • Contactin 2
  • Nerve Tissue Proteins
  • Nuclear Proteins
  • Amyloid Precursor Protein Secretases