GADD34 induces cell death through inactivation of Akt following traumatic brain injury

J. M. Farook, J. Shields, A. Tawfik, S. Markand, T. Sen, S. B. Smith, D. Brann, K. M. Dhandapani, N. Sen

Research output: Contribution to journalArticlepeer-review

55 Scopus citations


Neuronal cell death contributes significantly to the pathology of traumatic brain injury (TBI) irrespective of the mode or severity of the injury. Activation of a pro-survival protein, Akt, is known to be regulated by an E3 ligase TRAF6 through a process of ubiquitination-coupled phosphorylation at its T308 residue. Here we show that upregulation of a pro-apototic protein, GADD34, attenuates TRAF6-mediated Akt activation in a controlled cortical impact model of TBI in mice. TBI induces the expression of GADD34 by stimulating binding of a stress inducible transcription factor, ATF4, to the GADD34 promoter. GADD34 then binds with TRAF6 and prevents its interaction with Akt. This event leads to retention of Akt in the cytosol and prevents phosphorylation at the T308 position. Finally, in vivo depletion of GADD34 using a lentiviral knockdown approach leads to a rescue of Akt activation and markedly attenuates TBI-induced cell death.

Original languageEnglish (US)
Article numbere754
JournalCell Death and Disease
Issue number8
StatePublished - Aug 2013


  • Akt
  • Cell death
  • GADD34
  • TBI
  • TRAF6

ASJC Scopus subject areas

  • Immunology
  • Cellular and Molecular Neuroscience
  • Cell Biology
  • Cancer Research


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