Tau hot spots open new avenues of discovery into dementia

13 September 2022



Newly discovered cellular hot spots of a potentially toxic protein could open new research avenues into how Alzheimer’s disease progresses in the brain.

Scientists made the discovery while trying to understand how the protein Tau spreads throughout the brain at the Queensland Brain Institute’s Clem Jones Centre for Ageing Dementia Research (CJCADR).

Dr Pranesh Padmanabhan
Dr Pranesh Padmanabhan.

“Tau is particularly important because changes to this protein are thought to cause dementia,” lead author Dr Pranesh Padmanabhan said.

“Because of these modifications, this protein can aggregate and spread from cell to cell, potentially causing cell death.

“But how this protein transfers across cells has been unclear at the molecular level.”

Dementia search shifts to plasma membrane

Most research on Tau has been centred on its relationship and interactions with microtubules and possible signalling pathways of the cell.

The team, led by CJCADR Director Professor Jürgen Götz and Dr Padmanabhan, used super-resolution microscopy to focus on the plasma membrane – the barrier between the cell and its outside environment.

“We managed to look at individual Tau molecules very close to the plasma membrane, how they move and organise at a nanoscale level,” Dr Padmanabhan said.

“Firstly, we found that Tau localised to the plasma membrane and displayed highly heterogeneous behaviour in space and time.

“But a more intriguing finding was that these proteins started to form what is called a hot spot, within which Tau molecules are highly immobilised.

“We also found that lowering cholesterol, which reduces Tau pathology in Alzheimer’s disease mouse models, had little impact on these hot spots.”

New avenues for dementia discovery

Dr Padmanabhan said these discoveries have the potential to spark a better understanding of how dementia starts, and what prompts it to spread from cell to cell.

Intensity map of Tau-mEos3.2 molecules showing spatial heterogeneity in the organisation of Tau molecules.
Intensity map of Tau-mEos3.2 molecules showing spatial heterogeneity in the organisation of Tau molecules.

“Now, these hot spots could mean a lot in terms of Tau’s functions,” Dr Padmanabhan said.

“It could be the site where it is released, or these hot spots could be locations where Tau executes its multiple functions.

“Understanding what these hot spots mean requires further work, but at least it gives a starting point to think about the role of Tau in health and disease in a completely different way.”

Professor Götz said the findings demonstrated the importance of new technologies, such as super-resolution microscopy, in making new discoveries about the brain.

“This new research opens the way for gaining deeper insight into how Tau and other key proteins impair neuronal functions in a pathological context such as Alzheimer’s disease,” he said.

“It also emphasises why it’s critical to continue to invest in core facilities and technologies.”

The findings were first published in The EMBO Journal (https://doi.org/10.15252/embj.2022111265).

Media: QBI Communications, communications@qbi.uq.edu.a, Quinn Jones +61 (0)402 141 270, Elaine Pye +61 (0)415 222 606, Merrett Pye +61 (0)422 096 049.

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