DAPK1-p53 interaction converges necrotic and apoptotic pathways of ischemic neuronal death

J Neurosci. 2014 May 7;34(19):6546-56. doi: 10.1523/JNEUROSCI.5119-13.2014.

Abstract

Necrosis and apoptosis are two distinct types of mechanisms that mediate ischemic injury. But a signaling point of convergence between them has yet to be identified. Here, we show that activated death-associated protein kinase 1 (DAPK1), phosphorylates p53 at serine-23 (pS(23)) via a direct binding of DAPK1 death domain (DAPK1DD) to the DNA binding motif of p53 (p53DM). We uncover that the pS(23) acts as a functional version of p53 and mediates necrotic and apoptotic neuronal death; in the nucleus, pS(23) induces the expression of proapoptotic genes, such as Bax, whereas in the mitochondrial matrix, pS(23) triggers necrosis via interaction with cyclophilin D (CypD) in cultured cortical neurons from mice. Deletion of DAPK1DD (DAPK1(DDΔ)) or application of Tat-p53DM that interrupts DAPK1-p53 interaction blocks these dual pathways of pS(23) actions in mouse cortical neurons. Thus, the DAPK1-p53 interaction is a signaling point of convergence of necrotic and apoptotic pathways and is a desirable target for the treatment of ischemic insults.

Keywords: DAPK1; NMDA receptors; ischemia; neuronal death.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / genetics*
  • Brain Ischemia / genetics*
  • Brain Ischemia / pathology*
  • Cell Hypoxia / physiology
  • Cells, Cultured
  • Cloning, Molecular
  • Cyclophilins / metabolism
  • Death-Associated Protein Kinases / genetics
  • Death-Associated Protein Kinases / metabolism
  • Death-Associated Protein Kinases / physiology*
  • Dependovirus / genetics
  • Gene Deletion
  • Glucose / genetics
  • Glutathione Transferase / metabolism
  • Immunoprecipitation
  • Luciferases / genetics
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Necrosis / genetics*
  • Neurons / pathology*
  • Peptidyl-Prolyl Isomerase F
  • Protein Binding
  • Real-Time Polymerase Chain Reaction
  • Signal Transduction / genetics*
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / physiology*
  • bcl-2-Associated X Protein / biosynthesis
  • bcl-2-Associated X Protein / genetics

Substances

  • Peptidyl-Prolyl Isomerase F
  • PPIF protein, mouse
  • Tumor Suppressor Protein p53
  • bcl-2-Associated X Protein
  • Luciferases
  • Glutathione Transferase
  • Dapk1 protein, mouse
  • Death-Associated Protein Kinases
  • Cyclophilins
  • Glucose