Experimental evidence for the age dependence of tau protein spread in the brain.
Susanne WegmannRachel E BennettLouis DelormeAshley B RobbinsMiwei HuDanny McKenzieMolly J KirkJulia SchiantarelliNahel TunioAna C AmaralZhanyun FanSamantha NichollsEloise HudryBradley T HymanPublished in: Science advances (2019)
The incidence of Alzheimer's disease (AD), which is characterized by progressive cognitive decline that correlates with the spread of tau protein aggregation in the cortical mantle, is strongly age-related. It could be that age predisposes the brain for tau misfolding and supports the propagation of tau pathology. We tested this hypothesis using an experimental setup that allowed for exploration of age-related factors of tau spread and regional vulnerability. We virally expressed human tau locally in entorhinal cortex (EC) neurons of young or old mice and monitored the cell-to-cell tau protein spread by immunolabeling. Old animals showed more tau spreading in the hippocampus and adjacent cortical areas and accumulated more misfolded tau in EC neurons. No misfolding, at any age, was observed in the striatum, a brain region mostly unaffected by tangles. Age and brain region dependent tau spreading and misfolding likely contribute to the profound age-related risk for sporadic AD.
Keyphrases
- cerebrospinal fluid
- cognitive decline
- resting state
- white matter
- functional connectivity
- cerebral ischemia
- spinal cord
- single cell
- stem cells
- multiple sclerosis
- protein protein
- type diabetes
- climate change
- mesenchymal stem cells
- metabolic syndrome
- amino acid
- intellectual disability
- insulin resistance
- skeletal muscle
- late onset
- binding protein
- amyotrophic lateral sclerosis