The findings are being published online this week in Proceedings of the National Academy
of Sciences, a professional journal. They could open the door to major advances on some of the world's most significant degenerative
diseases, researchers say.
The OSU scientists, in collaboration with Molecular Probes-Invitrogen of Eugene, Ore.,
found a chemical process to directly see and visualize "superoxide" in actual cells. This oxidant, which was first discovered
80 years ago, plays a key role in both normal biological processes and - when it accumulates to excess - the destruction or
death of cells and various disease processes.
"In the past, our techniques for measuring or understanding superoxide were like blindly
hitting a box with a hammer and waiting for a reaction," said Joseph Beckman, a professor of biochemistry and director of
the OSU Environmental
Center. "Now we can really see and measure, in real time,
what's going on in a cell as we perform various experiments."
In research on amyotrophic lateral sclerosis, or Lou Gehrig's Disease, which is one of
his lab's areas of emphasis, Beckman said they have used the new technique to learn as much in the past three months about
the basic cell processes as they did in the previous 15 years. Hundreds of experiments can now rapidly be done that previously
would have taken much longer or been impossible.
"This will enable labs all over the world to significantly speed up their work on the
basic causes and processes of many diseases, including ALS, arthritis, diabetes, Parkinson's disease, Alzheimer's disease,
heart disease and others," Beckman said. "And it should be especially useful in studying aging, particularly the theory that
one cause of aging is mitochondrial decay."
The process of oxidation in the body, researchers say, is one that's fundamental to life
but also prone to problems. Oxygen in the cells can be reduced to a molecule called superoxide, which is part of normal immune
system processes and may also have other functions - it was first named by OSU alumnus Linus Pauling in 1934.
"Oxygen is actually one of the more toxic molecules
in the environment," Beckman said. "Breathing 100 percent pure oxygen will destroy your lungs in about three days because
it increases the formation of superoxide."
Superoxide is efficiently removed by an enzyme, superoxide dismutase. Antioxidants in
food, such as vitamin C and E, are also part of this process. [Studies of these
vitamins and their effect upon superoxide, however, have failed to show effect—jk.] And in healthy animals, including
humans, this delicate balancing act can work well and cause few problems. But sometimes the process breaks down and excess
levels of superoxide begin to accumulate and lead to a wide variety of degenerative diseases.
Prior to this, there was no direct and accurate way to measure superoxide or its origin
from the two places that produce it, the cell's cytosol or mitochondria. Now there is.
With the new system developed at OSU, researchers can
use a fluorescent microscope, a fairly standard laboratory tool, to actually see levels of superoxide and observe changes
as experiments are performed with living cells.
"If we poison the mitochondria, using something like the pesticides that have been implicated
in Parkinson's disease, we can actually see superoxide levels begin to rapidly rise,"
Beckman said. "You get a similar reaction if a growth factor is added that's implicated
in the development of Lou Gehrig's Disease."
The data available from this new technology, Beckman said, are so profound that for some
time many in the science community didn't believe it was possible.
"This will become a critical tool in learning how superoxide works in a cell," he said.
"I've been studying this for more than 10 years and never thought we would have such a clear and accurate picture of what's
going on inside a living cell."
In their research on ALS, for instance, OSU scientists have used the new system to actually
see cells eating themselves alive and dying from excess superoxide production. A new compound is in phase one clinical trials
that appears to inhibit this process and may ultimately provide a therapy for the disease.
Oxidative stress resulting from mitochondrial dysfunction
has already been implicated in neurodegeneration, aging, diabetes and cancer, the researchers said in their report.
The new findings could rapidly speed research in all of those fields, they said.
Source: Oregon State