Researchers believe imaging could lead to better understanding of what causes fatal prion diseases
Prion diseases are incurable, deadly neurological disorders that can affect both humans and animals–including Creutzfeldt-Jakob Disease in people, Bovine Spongiform Encephalopathy in cows (also known as Mad Cow Disease), and Chronic Wasting Disease in deer.
Scientists have spent decades working to better understand how prions cause these diseases. But new research from Case Western Reserve University School of Medicine and the National Institutes of Health (NIH) Rocky Mountain Laboratories brings into focus how prions might be formed and how they can result in different disease outcomes.
“Prions are unusual pathogens. Different prions result in different disease lengths and symptoms in their host,” said Allison Kraus, assistant professor of pathology at the School of Medicine, who co-led the research with Byron Caughey at NIH. “This has long perplexed scientists because different diseases occur with corruption of the same protein from its original shape.”
“Our study identifies the key similarities and differences in prions and how these features compare to other types of self-converting proteins,” Kraus said. “We can now begin to appreciate how those key similarities and differences shape disease outcomes of prion disease and compare the outcomes to other brain diseases.”
Prion disease occurs when prion proteins are refolded, causing a chain reaction where other prion proteins refold and accumulate in the brain, according to the NIH.
Kraus said the new prion imaging could play a key role towards understanding prion disease outcomes.
“Neurodegenerative brain diseases are incredibly complex,” she said. “With indications that corrupted shapes do indeed occur with different prion diseases, and with further research into more prion strains, we can begin to understand how specific prion shapes relate to disease outcomes.”
Study authors include: Kraus, Heidi Standke, Kunpeng Li, Matteo Manca and Olivia Thomas from Case Western Reserve; and Forrest Hoyt, Efrosini Artikis, Cindi Schwartz, Bryan Hansen, Andrew Hughson, Gregory Raymond, Brent Race, Gerald Baron and Caughey from NIH.