Phosphorylation of SET mediates apoptosis via P53 hyperactivation and NM23-H1 nuclear import

Neurobiol Aging. 2018 Sep:69:38-47. doi: 10.1016/j.neurobiolaging.2018.04.022. Epub 2018 May 8.

Abstract

Apoptosis plays an important role in neuron loss in Alzheimer's disease (AD). SET, an endogenous inhibitor of protein phosphatase-2A, is phosphorylated in AD brains and positively correlates with cell apoptosis. However, the mechanism underlying phosphorylated SET association with apoptosis remains unknown. Here, we show that mimetic phosphorylation of SET (S9E) induced apoptosis of primary cultured neurons. To investigate its mechanism, we overexpressed SET (S9E) in HEK293/tau cells and observed apoptosis accompanied with a marked increase of cleaved caspase-3 and cytoplasmic SET (S9E) retention with enhanced protein phosphatase-2A inhibition, which subsequently caused p53 hyperphosphorylation and activation. In addition, it caused the release of nucleoside diphosphate kinase A isoform a, a positive regulator of p53 with a DNase activity from SET/nucleoside diphosphate kinase A isoform a complex, and migration into the nucleus, resulting in DNA damage. Besides, it reduced nuclear tau accumulation leading to DNA protection deficiency. These findings suggest that SET phosphorylation is involved in the neuronal apoptotic pathway in AD and provide a new insight into the mechanism of this pathology.

Keywords: Alzheimer's disease; Apoptosis; NM23-H1; SET; Tau; p53.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus*
  • Alzheimer Disease / metabolism*
  • Animals
  • Apoptosis Regulatory Proteins
  • Apoptosis*
  • Carrier Proteins / metabolism*
  • Cerebral Cortex / metabolism
  • DNA-Binding Proteins
  • HEK293 Cells
  • Histone Chaperones / metabolism*
  • Humans
  • NM23 Nucleoside Diphosphate Kinases / metabolism*
  • Nuclear Proteins / metabolism*
  • Phosphorylation
  • Primary Cell Culture
  • Rats, Sprague-Dawley
  • Transcription Factors / metabolism*
  • Tumor Suppressor Protein p53 / metabolism*
  • tau Proteins / metabolism

Substances

  • Apoptosis Regulatory Proteins
  • Carrier Proteins
  • DNA-Binding Proteins
  • Histone Chaperones
  • MAPT protein, human
  • NM23 Nucleoside Diphosphate Kinases
  • Nuclear Proteins
  • SET protein, human
  • SET protein, rat
  • Transcription Factors
  • Tumor Suppressor Protein p53
  • tau Proteins
  • NME1 protein, human