Role of the prolyl isomerase Pin1 in protecting against age-dependent neurodegeneration

Nature. 2003 Jul 31;424(6948):556-61. doi: 10.1038/nature01832.


The neuropathological hallmarks of Alzheimer's disease and other tauopathies include senile plaques and/or neurofibrillary tangles. Although mouse models have been created by overexpressing specific proteins including beta-amyloid precursor protein, presenilin and tau, no model has been generated by gene knockout. Phosphorylation of tau and other proteins on serine or threonine residues preceding proline seems to precede tangle formation and neurodegeneration in Alzheimer's disease. Notably, these phospho(Ser/Thr)-Pro motifs exist in two distinct conformations, whose conversion in some proteins is catalysed by the Pin1 prolyl isomerase. Pin1 activity can directly restore the conformation and function of phosphorylated tau or it can do so indirectly by promoting its dephosphorylation, which suggests that Pin1 is involved in neurodegeneration; however, genetic evidence is lacking. Here we show that Pin1 expression is inversely correlated with predicted neuronal vulnerability and actual neurofibrillary degeneration in Alzheimer's disease. Pin1 knockout in mice causes progressive age-dependent neuropathy characterized by motor and behavioural deficits, tau hyperphosphorylation, tau filament formation and neuronal degeneration. Thus, Pin1 is pivotal in protecting against age-dependent neurodegeneration, providing insight into the pathogenesis and treatment of Alzheimer's disease and other tauopathies.

Publication types

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

MeSH terms

  • Aging / physiology*
  • Alzheimer Disease / enzymology
  • Alzheimer Disease / pathology
  • Alzheimer Disease / physiopathology
  • Alzheimer Disease / prevention & control
  • Amino Acid Motifs
  • Animals
  • Behavior, Animal / physiology
  • Gene Deletion
  • Gene Expression
  • Humans
  • Mice
  • Mice, Knockout
  • Microscopy, Electron
  • Motor Activity / physiology
  • NIMA-Interacting Peptidylprolyl Isomerase
  • Neurofibrillary Tangles / metabolism
  • Neurofibrillary Tangles / pathology
  • Neurons / metabolism
  • Neurons / pathology
  • Neuroprotective Agents / metabolism
  • Peptidylprolyl Isomerase / genetics
  • Peptidylprolyl Isomerase / metabolism*
  • Phosphoproteins / chemistry
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Phosphoserine / metabolism
  • Phosphothreonine / metabolism
  • Plaque, Amyloid / metabolism
  • Plaque, Amyloid / pathology
  • Tauopathies / enzymology*
  • Tauopathies / pathology
  • Tauopathies / physiopathology
  • Tauopathies / prevention & control*


  • NIMA-Interacting Peptidylprolyl Isomerase
  • Neuroprotective Agents
  • Phosphoproteins
  • Phosphothreonine
  • Phosphoserine
  • PIN1 protein, human
  • Peptidylprolyl Isomerase
  • Pin1 protein, mouse