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Neuronal uptake and propagation of a rare phosphorylated high-molecular-weight tau derived from Alzheimer's disease brain

  • Shuko Takeda
  • , Susanne Wegmann
  • , Hansang Cho
  • , Sarah L. Devos
  • , Caitlin Commins
  • , Allyson D. Roe
  • , Samantha B. Nicholls
  • , George A. Carlson
  • , Rose Pitstick
  • , Chloe K. Nobuhara
  • , Isabel Costantino
  • , Matthew P. Frosch
  • , Daniel J. Muller
  • , Daniel Irimia
  • , Bradley T. Hyman
  • Massachusetts General Hospital
  • University of North Carolina at Charlotte
  • McLaughlin Research Institute
  • Swiss Federal Institute of Technology Zurich

Research output: Contribution to journalArticlepeer-review

Abstract

Tau pathology is known to spread in a hierarchical pattern in Alzheimer's disease (AD) brain during disease progression, likely by trans-synaptic tau transfer between neurons. However, the tau species involved in inter-neuron propagation remains unclear. To identify tau species responsible for propagation, we examined uptake and propagation properties of different tau species derived from postmortem cortical extracts and brain interstitial fluid of tau-transgenic mice, as well as human AD cortices. Here we show that PBS-soluble phosphorylated high-molecular-weight (HMW) tau, though very low in abundance, is taken up, axonally transported, and passed on to synaptically connected neurons. Our findings suggest that a rare species of soluble phosphorylated HMW tau is the endogenous form of tau involved in propagation and could be a target for therapeutic intervention and biomarker development.

Original languageEnglish
Article number8490
JournalNature Communications
Volume6
DOIs
StatePublished - 13 Oct 2015
Externally publishedYes

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