Researchers find new role for protein in combating age-related diseases

by

Editors' notes

This article has been reviewed according to Science X's editorial process and policies. Editors have highlighted the following attributes while ensuring the content's credibility:

fact-checked

peer-reviewed publication

trusted source

proofread

C. elegans examined under a microscope. The yellow and purple dots are the regions where MANF protein is located. Credit: McMaster University

McMaster University researchers have discovered a previously unknown cell-protecting function of a protein, which could open new avenues for treating age-related diseases and lead to healthier aging overall.

The team has found that a class of protective proteins known as MANF plays a role in the process that keep cells efficient and working well.

The findings appear in the journal Proceedings of the National Academy of Sciences.

Our cells make proteins and discard them after they perform their jobs. This efficient, continuous maintenance process is known as cellular homeostasis. However, as we age, our cells' ability to keep up declines.

Cells can create proteins incorrectly, and the cleanup process can become faulty or overwhelmed. As a result, proteins can clump together, leading to a harmful buildup that has been linked to such diseases as Alzheimer's and Parkinson's.

"If the cells are experiencing stress because this protein aggregation has started, the endoplasmic reticulum, which is where proteins are made and then released, gets the signal to stop making these proteins," explains biology professor Bhagwati Gupta, who supervised the research.

"If it can't correct the problem, the cell will die, which ultimately leads to degeneration of the neurons and then neurodegenerative diseases that we see."

Previous studies, including one from McMaster, have shown that MANF protects against increased cellular stress. The team set out to understand how this happens by studying microscopic worms known as C. elegans. They created a system to manipulate the amount of MANF in C. elegans.

"We could literally see where MANF was expressed in the worms because they are translucent. We could see it in all different tissues. Within these tissues, MANF was present in structures known as lysosomes which are associated with lifespan and protein aggregation," said Shane Taylor, now a post-doctoral fellow at the University of British Columbia who worked on the project for his Ph.D. while at McMaster.

The team discovered that MANF plays a key role in the cell's disposal process by helping to break down the accumulated proteins, keeping cells healthier and clutter-free.

Increasing MANF levels also activates a natural clean-up system within cells, helping them function better for longer.

"Although our research focused on worms, the findings uncover universal processes. MANF is present in all animals, including humans. We are learning fundamental and mechanistic details that could then be tested in higher systems," said Taylor.

To develop MANF as a potential therapy, researchers want to understand what other players MANF interacts with.

"Discovering MANF's role in cellular homeostasis suggests that it could be used to develop treatments for diseases that affect the brain and other parts of the body by targeting cellular processes, clearing out these toxic clumps in cells and maintaining their health," said Gupta.

"The central idea of aging research is basically, can we make the processes better and more efficient. By understanding how MANF works and targeting its function, we could develop new treatments for age-related diseases. We want to live longer and healthier. These kinds of players could help that."

More information: Shane K. B. Taylor et al, The neurotrophic factor MANF regulates autophagy and lysosome function to promote proteostasis in Caenorhabditis elegans, Proceedings of the National Academy of Sciences (2024). DOI: 10.1073/pnas.2403906121

Journal information: Proceedings of the National Academy of Sciences

Provided by McMaster University