Frontiers in Aging Neuroscience (Jul 2022)

The Fate of Tau Aggregates Between Clearance and Transmission

  • Assel Seitkazina,
  • Assel Seitkazina,
  • Kyu Hyeon Kim,
  • Kyu Hyeon Kim,
  • Erin Fagan,
  • Yoonsik Sung,
  • Yoonsik Sung,
  • Yun Kyung Kim,
  • Yun Kyung Kim,
  • Sungsu Lim

DOI
https://doi.org/10.3389/fnagi.2022.932541
Journal volume & issue
Vol. 14

Abstract

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Neuronal accumulation of mis-folded tau is the pathological hallmark of multiple neurodegenerative disorders, including Alzheimer’s disease. Distinct from amyloid plaques, which appear simultaneously throughout the brain, tau pathology develops first in a specific brain region and then propagates to neuroanatomically connected brain regions, exacerbating the disease. Due to the implication in disease progression, prevention of tau transmission is recognized as an important therapeutic strategy that can halt disease progression in the brain. Recently, accumulating studies have demonstrated diverse cellular mechanisms associated with cell-to-cell transmission of tau. Once transmitted, mis-folded tau species act as a prion-like seed for native tau aggregation in the recipient neuron. In this review, we summarize the diverse cellular mechanisms associated with the secretion and uptake of tau, and highlight tau-trafficking receptors, which mediate tau clearance or cell-to-cell tau transmission.

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