Recycling a Cell's Energy Centers to Ward Off Parkinson's Disease

SAN FRANCISCO, Aug. 6, 2021 /PRNewswire/ -- Scientists have long known that living cells are master recyclers, constantly breaking down old parts and building them back up into new molecular machines. Now, researchers at Gladstone Institutes have taken a closer look at the life cycle of energy-generating cellular power plants—called mitochondria— inside brain cells, and how they might be recycled. They showed that genes associated with Parkinson's disease play key roles in this process.

"This work gives us unprecedented insight into mitochondria's life cycle and how they are recycled by key proteins that, when mutated,  cause Parkinson's disease," says Gladstone Associate Investigator Ken Nakamura, MD, PhD, senior author of the new study. "It suggests that mitochondrial recycling is critical to maintaining healthy mitochondria, and disruptions to this process can contribute to neurodegeneration."

Breaking Down Damaged Mitochondria

In most cells, damaged mitochondria are decomposed in a process known as mitophagy, which is initiated by two proteins, PINK1 and Parkin. Mutations in these same proteins also cause hereditary forms of Parkinson's disease. While the role of PINK1 and Parkin in mitophagy has been heavily studied in many cell types, it has been unclear whether these proteins act the same way in neurons—the type of brain cells that die in Parkinson's disease. Indeed, neurons have unusually high energy needs and their mitochondria are much more resistant to degradation by Parkin than those in other cell types.

In the new study published in the journal Science Advances, Nakamura's group followed mitochondria inside living neurons and examined how PINK1 and Parkin affected their fate.

But mitochondria are small and they move inside cells, frequently fusing with each other or splitting in two, which makes them difficult to track.

"We had to develop a new way of tracking individual mitochondria over long periods of time, almost a full day," says Zak Doric, a graduate student at Gladstone and UC San Francisco (UCSF) and co-first author of the new study. "Getting that technique up and running was quite a challenge."

The scientists also used a method that allowed them to generate larger-than-normal mitochondria, making them easier to see under a microscope.

They found that Parkin proteins encircled damaged mitochondria and targeted them for degradation, demonstrating that mitophagy starts in neurons in the same way as in other cell types. But thanks to their new approach, they could watch the process unfold in great detail. For instance, they documented the key initial steps in which damaged, Parkin-coated mitochondria fuse with other components inside the cell to form mitochondria-degrading structures called mitolysosomes.

"We were able to visualize these steps at a level that hasn't been done before in any cell type," says Nakamura, who is also an associate professor of neurology at UCSF.

The high resolution of their approach will allow them to understand with great precision how Parkin and PINK1 affect mitochondrial degradation in Parkinson's disease.

A New Kind of Recycling

The researchers then examined the later phases of mitophagy, monitoring what happens to mitochondria in the mitolysosomes.

"Until now, nobody has known what happens next to these mitolysosomes," says Nakamura.

So far, scientists had assumed that mitolysosomes rapidly break down into molecules that the cell can reuse to build new mitochondria from scratch. Nakamura and his team showed that, instead, the mitolysosomes survived for hours inside cells. Remarkably, and unexpectedly, some mitolysosomes were engulfed by healthy mitochondria, while other times, they suddenly burst, releasing their contents into the interior of the cell, including some proteins that were still functional.

"This appears to be a new mitochondrial quality control, recycling system," says Huihui Li, PhD, a Gladstone postdoctoral scholar and co-first author of the new paper. "We think we've uncovered a pathway of mitochondrial recycling—which is like salvaging valuable furniture in a house before demolishing it."

Importantly, the study shows that the recycling pathway identified by the scientists requires PINK1 and Parkin, supporting that mitochondrial recycling may also be critical in protecting against neurodegeneration in Parkinson's disease.

"Dopamine neurons that die in Parkinson's disease are particularly susceptible to mutations in PINK1 and Parkin," says Nakamura. "Our study advances our understanding of how these two key Parkinson's disease proteins degrade and recycle mitochondria. Our future studies will investigate how these pathways contribute to disease and how they can be targeted therapeutically."

About the Study

The paper "Longitudinal Tracking of Neuronal Mitochondria Delineates PINK1/Parkin-Dependent Mechanisms of Mitochondrial Recycling and Degredation" was published by the journal Science Advances on August 6, 2021.

Other authors are: Amandine Berthet, Mai Nguyen, Julia Margulis, Rebecca Fang, and Steve Finkbeiner of Gladstone; Danielle Jorgens of UC Berkeley; Ivy Hsieh, Jayanta Debnath, and Eric Huang of UC San Francisco; and Hiromi Sesaki of Johns Hopkins.

The work at Gladstone was supported by the Joan and David Traitel Family Trust, Betty Brown's Family, a Career Awards for Medical Scientists from the Burroughs-Wellcome Fund, the National Institutes of Health (RO1NS091902, 5P30 NS069496), the Hillblom Foundation, and a Berkelhammer Award for Excellence in Neuroscience.

About Gladstone Institutes

To ensure our work does the greatest good, Gladstone Institutes focuses on conditions with profound medical, economic, and social impact—unsolved diseases. Gladstone is an independent, nonprofit life science research organization that uses visionary science and technology to overcome disease. It has an academic affiliation with the University of California, San Francisco.

Media Contact: Julie Langelier | Associate Director, Communications | julie.langelier@gladstone.org | 415.734.5000

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SOURCE Gladstone Institutes