Co-Expression of Three Wild-Type 3R-Tau Isoforms Induces Memory Deficit via Oxidation-Related DNA Damage and Cell Death: A Promising Model for Tauopathies

J Alzheimers Dis. 2020;73(3):1105-1123. doi: 10.3233/JAD-191132.

Abstract

The three isoforms of 3R-tau are predominantly deposited in neurons bearing neurofibrillary tangles in Alzheimer's disease (AD), while only 3R-tau accumulation has been detected in Pick's disease (PiD), suggesting the involvement of 3R-tau in neurodegeneration. However, both the role and the molecular mechanism of 3R-tau in neurodegeneration are elusive. Here, we co-expressed three isoforms of human wild-type 3R-tau in adult mouse hippocampal to mimic the pathologic tau accumulating observed in PiD patients. We found that co-expressing three 3R-tau isoforms induced hyperphosphorylation and accumulation of tau proteins; simultaneously, the mice showed remarkable neuron death with synapse and memory deficits. Further in vitro and in vivo studies demonstrated that co-expressing 3R-tau isoforms caused oxidative stress evidenced by an increased malondialdehyde, and the decreased superoxide dismutase and glutathione peroxidase; the 3R-tau accumulation also induced significant glial activation and DNA double-strand breaks (DSBs). Notably, the toxic effects of 3R-tau accumulation were efficiently reversed by administration of antioxidants Vitamin E (VitE) and Vitamin C (VitC), respectively. These data reveal that intracellular accumulation of 3R-tau isoforms in adult brain induces significant neuron death and memory deficits with the mechanism involving oxidation-mediated DSBs; and the antioxidants VitE and VitC can efficiently attenuate the toxicities of 3R-tau. Given that no significant cell death has been detected in the currently available wild-type tau-accumulating models, co-expressing 3R-tau isoforms could be a promising model for drug development of tauopathies, such as PiD.

Keywords: 3R-tau; DNA double-strand breaks; oxidative stress; tauopathies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Death / physiology*
  • DNA Damage / physiology*
  • Disease Models, Animal
  • Hippocampus / metabolism
  • Hippocampus / pathology
  • Memory Disorders / genetics
  • Memory Disorders / metabolism*
  • Mice
  • Neurons / metabolism
  • Neurons / pathology
  • Oxidative Stress / physiology
  • Phosphorylation
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism*
  • Tauopathies / genetics
  • Tauopathies / metabolism*
  • Tauopathies / pathology
  • tau Proteins / genetics
  • tau Proteins / metabolism*

Substances

  • Protein Isoforms
  • tau Proteins