Smuggle tau through a secret(ory) pathway

Biochem J. 2021 Jul 30;478(14):2921-2925. doi: 10.1042/BCJ20210324.

Abstract

Secretion of misfolded tau, a microtubule-binding protein enriched in nerve cells, is linked to the progression of tau pathology. However, the molecular mechanisms underlying tau secretion are poorly understood. Recent work by Lee et al. [Biochemical J. (2021) 478: 1471-1484] demonstrated that the transmembrane domains of syntaxin6 and syntaxin8 could be exploited for tau release, setting a stage for testing a novel hypothesis that has profound implications in tauopathies (e.g. Alzheimer's disease, FTDP-17, and CBD/PSP) and other related neurodegenerative diseases. The present commentary highlights the importance and limitations of the study, and discusses opportunities and directions for future investigations.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alzheimer Disease / genetics
  • Alzheimer Disease / metabolism*
  • Alzheimer Disease / pathology
  • Animals
  • Cells, Cultured
  • Endosomes / metabolism
  • HEK293 Cells
  • Humans
  • Mice
  • Microscopy, Fluorescence
  • Neurons / cytology
  • Neurons / metabolism
  • Protein Binding
  • Qa-SNARE Proteins / genetics
  • Qa-SNARE Proteins / metabolism*
  • Secretory Pathway*
  • Tauopathies / genetics
  • Tauopathies / metabolism*
  • Tauopathies / pathology
  • tau Proteins / genetics
  • tau Proteins / metabolism*
  • trans-Golgi Network / metabolism

Substances

  • Qa-SNARE Proteins
  • tau Proteins