Faculty of Medicine

Researchers Find Mechanism Behind Neuron Death in ALS and Dementia

Apr 19, 2018
Professor Peter St George-HyslopResearchers at the University of Toronto and the University of Cambridge have identified the molecular mechanism that leads to the death of neurons in some types of ALS, or amyotrophic lateral sclerosis, and in a common form of frontotemporal dementia. They have also uncovered novel therapeutic targets for these currently incurable diseases.

The journal Cell published the findings today.

A common characteristic of ALS and frontotemporal dementia is the clumping of misfolded RNA-binding proteins, including a protein called FUS, in the brain and spinal cord. In nerve cells, FUS proteins normally change back and forth from small liquid droplets (resembling oil droplets in water) to small gels (like jelly).

But in ALS and frontotemporal dementia, FUS proteins become permanently stuck as abnormally dense gels, trapping the RNA and making it unavailable for use. This damages nerve cells by blocking their ability to make the proteins needed for synaptic function and leads to the death of neurons in the brain and spinal cord.

“This was a very exciting set of experiments where we were able to apply cutting edge tools from physics, chemistry and neurobiology to understand how the FUS protein normally works in nerve cells, and how it goes wrong in motor neuron disease and dementia,” says Peter St George-Hyslop, director of the Tanz Centre for Research in Neurodegenerative Diseases and a professor of medicine at U of T. 

In healthy neurons, the FUS protein condenses (from droplets to gel), captures RNA and transfers it to remote parts of the neuron involved in making connections (synapses) with other neurons. Here, the protein ‘melts’ and releases the RNA. The RNA then helps create new proteins in the synapses, which are essential for keeping the synapses working properly, especially during memory formation and learning.  

In frontotemporal dementia, the researchers found that defects in the chemical modification of FUS caused the abnormal gelling. In motor neuron disease, abnormal gelling arose from mutations in the FUS protein itself, which meant it was no longer able to change form. “These findings open up a new avenue of work to identify ways to prevent the abnormal gelling of FUS in motor neuron disease and dementia,” says St George-Hyslop, who is also a professor at the Institute for Medical Research at the University of Cambridge.

The scientists used human cells that resemble neurons, and neurons from frogs, to investigate the regulation of FUS from liquid droplets to small gels — and what makes that reversible process go awry. Potential therapeutic targets include the enzymes that regulate the chemical modification of FUS, and the molecular chaperones that facilitate FUS proteins to change form.

These treatments would need to allow FUS to continue moving between safe reversible states (liquid droplets and reversible gels) but prevent FUS from dropping into the dense, irreversible gel states that cause disease.

“For the past several years, evidence has been growing that understanding these phase transitions could significantly accelerate our ability to treat ALS,” says Dr. David Taylor, vice president, research at the ALS Society of Canada. “The work advances our understanding of this biology and reveals potential molecular targets for exploration, which might someday lead to the development of ALS treatments.”

Taylor notes that the research was possible in part through funding from the Ice Bucket Challenge and the ALS Society of Canada’s partnership with Brain Canada, and he says the findings are an example of why continued investment in research funding is vital.

The research was funded by the Canadian Institutes of Health Research, Wellcome Trust, European Research Council, Swiss National Science Foundation, and the ALS Society of Canada and Brain Canada (through the Canada Brain Research Fund, with support from Health Canada).

*This story was based on a media release from the Wellcome Trust, written by Natalie Hodgson.

Aug 27 Let's #VoteScience: Empowering Canadians to Advocate for Science
Other | 5:15pm–7:30pm
Aug 31 Invisible Challenges In Medicine
Conference | 9:30am–4:00pm
11 – 14
International Society for the Advancement of Clinical MEG: Epilepsy and Beyond
Symposium | 7:00am–5:00pm
Sep 13 Cardio-Rheumatology Symposium
Symposium | 9:00am–3:00pm
Sep 18 Leadership, Success and Representation: Black Faculty & Learners
Other | 5:30pm–8:00pm
20 – 22
34th Annual Organ Imaging Review
Conference | 7:15am–5:15pm
Sep 20 Promoting Safer Opioid Prescribing for Patients with Cancer
Grand Rounds | 8:00am–9:00am


UofT Medicine
RT : Watching this brought back so many happy memories!! Congratulations to the class of 2023! is where I met… https://t.co/lEwWrgVCjq
UofT Medicine
Life-long friendships are made at ! Who were the friends you’ve made in medical school, that you’ll keep fo… https://t.co/TOilIsz07y
UofT Medicine
The first day of O-Week has been a blast - and it's not over yet! Share your O-Week highlights and tag… https://t.co/8NYn5wEbJD

UofTMed Magazine

Have we lost the art of dying?

Sign up for your free digital copy.