Palmitoylation of the C-terminal fragment of p75(NTR) regulates death signaling and is required for subsequent cleavage by gamma-secretase

Mol Cell Neurosci. 2008 Feb;37(2):346-58. doi: 10.1016/j.mcn.2007.10.005. Epub 2007 Oct 23.


It has recently been shown that the p75 neurotrophin receptor (p75(NTR)), which is known to mediate neural cell death during development of the nervous system and in a range of adult neurodegenerative conditions, undergoes a regulated process of cell surface receptor cleavage, regulated intramembrane proteolysis (RIP). Here we show that neuronal death signaling occurs only following extracellular metalloprotease cleavage of p75(NTR) and palmitoylation of the resultant C-terminal fragment, causing its translocation to cholesterol-rich domains of the plasma membrane. Furthermore, death signaling is promoted by inhibition of intracellular gamma-secretase cleavage, a process which also occurs within the cholesterol-rich domains. In the presence of TrkA signaling, C-terminal fragment localization in these cholesterol-rich domains is prevented, thereby blocking neuronal death. Thus p75(NTR) activates neuronal death pathways in conditions where the balance of normal RIP is shifted toward extracellular domain cleavage due to increased metalloprotease activity, decreased TrkA activity or compromised gamma-secretase activity, all of which are features of neurodegenerative conditions such as Alzheimer's disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid Precursor Protein Secretases / genetics
  • Amyloid Precursor Protein Secretases / metabolism*
  • Animals
  • Animals, Newborn
  • Cell Death / genetics*
  • Cell Line
  • Cells, Cultured
  • Extracellular Space / metabolism
  • Humans
  • Intracellular Fluid / metabolism
  • Lipoylation / genetics*
  • Membrane Microdomains / genetics
  • Membrane Microdomains / metabolism*
  • Metalloproteases / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Nerve Degeneration / genetics
  • Nerve Degeneration / metabolism*
  • Nerve Degeneration / physiopathology
  • Peptide Hydrolases / metabolism
  • Protein Structure, Tertiary / genetics
  • Rats
  • Receptor, trkA / metabolism
  • Receptors, Nerve Growth Factor / chemistry
  • Receptors, Nerve Growth Factor / genetics
  • Receptors, Nerve Growth Factor / metabolism*
  • Signal Transduction / genetics


  • Receptors, Nerve Growth Factor
  • TNFRSF16 protein, mouse
  • Receptor, trkA
  • Amyloid Precursor Protein Secretases
  • Metalloproteases
  • Peptide Hydrolases