Reducing acetylated tau is neuroprotective in brain injury

Cell. 2021 May 13;184(10):2715-2732.e23. doi: 10.1016/j.cell.2021.03.032. Epub 2021 Apr 13.

Abstract

Traumatic brain injury (TBI) is the largest non-genetic, non-aging related risk factor for Alzheimer's disease (AD). We report here that TBI induces tau acetylation (ac-tau) at sites acetylated also in human AD brain. This is mediated by S-nitrosylated-GAPDH, which simultaneously inactivates Sirtuin1 deacetylase and activates p300/CBP acetyltransferase, increasing neuronal ac-tau. Subsequent tau mislocalization causes neurodegeneration and neurobehavioral impairment, and ac-tau accumulates in the blood. Blocking GAPDH S-nitrosylation, inhibiting p300/CBP, or stimulating Sirtuin1 all protect mice from neurodegeneration, neurobehavioral impairment, and blood and brain accumulation of ac-tau after TBI. Ac-tau is thus a therapeutic target and potential blood biomarker of TBI that may represent pathologic convergence between TBI and AD. Increased ac-tau in human AD brain is further augmented in AD patients with history of TBI, and patients receiving the p300/CBP inhibitors salsalate or diflunisal exhibit decreased incidence of AD and clinically diagnosed TBI.

Keywords: Alzheimer’s disease; P7C3; acetylation; congenital muscular dystrophy; diflunisal; neurodegeneration; neuroprotection; omigapil; salsalate; tau; traumatic brain injury.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Alzheimer Disease / etiology*
  • Alzheimer Disease / metabolism
  • Alzheimer Disease / prevention & control*
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Biomarkers / blood
  • Biomarkers / metabolism
  • Brain Injuries, Traumatic / complications*
  • Brain Injuries, Traumatic / metabolism
  • Cell Line
  • Diflunisal / therapeutic use
  • Female
  • Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neurons / metabolism
  • Neuroprotection*
  • Salicylates / therapeutic use
  • Sirtuin 1 / metabolism
  • p300-CBP Transcription Factors / antagonists & inhibitors
  • p300-CBP Transcription Factors / metabolism
  • tau Proteins / blood
  • tau Proteins / metabolism*

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Biomarkers
  • Salicylates
  • tau Proteins
  • Diflunisal
  • Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)
  • p300-CBP Transcription Factors
  • p300-CBP-associated factor
  • Sirtuin 1
  • salicylsalicylic acid