Speeding Up Treatments for ALS – Innovita Research

Therapeutic solutions for amyotrophic lateral sclerosis (ALS or Lou Gehrig's disease) could be on the horizon thanks to unexpected findings by University of Arizona researchers. Disease-prompting bundles of proteins found within cells are cleared by unexpected processes.

TDP-43 is the red protein being expressed in yeast. Some of it is being sent to inside an organelle called the vacuole in yeast (lysosome in humans), which is the blue circle. Image credit: Ross Buchan/University of Arizona

ALS is the progressive degeneration of motor neurons that causes people to lose the ability to move and eventually speak, eat and breathe.

Within the neuronal cells of patients with ALS and other neurodegenerative diseases, two proteins – TDP-43 and FUS – are often found in bundles of molecular junk called aggregates, which can accumulate to deadly levels.

“It’s not clear yet if TDP-43 aggregates themselves are truly toxic or a sign that things have gotten really bad in a cell, and this is its last Hail Mary trying to keep things in order,” said Ross Buchan, assistant professor of molecular and cellular biology and a member of the BIO5 Institute. “These aggregates could possibly be toxic because they are trapping other useful molecules and not letting them do their job.”

Buchan and his team set out to investigate how healthy cells clear harmful aggregates from the cell.

What they found was that the aggregates were being removed via endocytosis, which was surprising for two reasons. First, the textbook definition of endocytosis is a process in which proteins, nutrients and chemical signals from outside the cell are brought inside to be degraded and recycled by the lysosome. But in this care, endocytosis was working on aggregates that were already inside the cell. And second, there’s already a mechanism, called autophagy, in place for recycling junk that originated from within a cell, yet endocytosis was doing what autophagy should have been doing instead.

“Autophagy – and also likely, although it’s still uncertain, endocytosis – often slows as we age, and there are genes that are mutated in that pathway that are associated with some neurodegenerative diseases. So people thought the reason aggregates form when we get old, or when you have these diseases, is because that pathway isn’t working very well,” Buchan said.

Additionally, the accumulation of aggregates slows the endocytosis pathway further, creating a negative feedback loop within the cell.

“If we genetically or chemically impede the pathway, then the TDP-43 protein accumulates and becomes super toxic. The cool thing, as far as a therapy for ALS is concerned, is that we can also do the reverse,” Buchan said. “We can make the endocytosis pathway work better by over-expressing parts of it, like putting the gas pedal down so it goes really fast. When we do that, then the TDP-43 aggregates are cleared really efficiently and it’s no longer toxic.”

Many of the paper’s experiments were performed in yeast cells, but the general findings are likely translatable to human cells based on initial findings. Buchan called yeast “a powerful genetic tool,” for understanding cellular processes, including those in human disease.

While the results from Buchan’s lab are unexpected – “If I were to pull a textbook off the self, it would say endocytosis is for things that are outside the cell, not inside, so it’s still pretty heretical,” he said – there are other labs with data suggesting endocytosis can also clear already internalized proteins.

The next step is to determine how TPD-43 and FUS enter the endocytic pathway, and then to develop ways to make endocytosis work better in these cells.

“There are genetic ways to do that, but not chemically at the moment,” Buchan said. “We think if we have a drug that inhibits the negative regulators of endocytosis, the pathway will go faster as a result. We have a couple ideas of where to start next.”

Graduate student Aaron Byrd, assistant professor of molecular and cellular biology and a BIO5 Institute member Ross Buchan and undergraduate senior Amanda Warner in the lab. (Photo: Michele Vaughan/University of Arizona)


G. Liu, A. Byrd, A.N. Warner, F. Pei, Eman Basha, A. Buchanan, J.R. Buchan. Cdc48/VCP and Endocytosis Regulate TDP-43 and FUS Toxicity and Turnover. Molecular and Cellular Biology Jan 2020, 40 (4) e00256-19

Source: University of Arizona, by Mikayla Mace.