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blindness

Method may delay onset of inherited blindness

Scientists have shown that boosting cells’ ability to process misfolded proteins could keep them from aggregating inside the cell, significantly delaying the onset of blindness in mice.

More than two million people worldwide live with inherited and untreatable retinal conditions, including retinitis pigmentosa, which slowly erodes vision.

“You can offer almost nothing in terms of treatment to a patient with retinitis pigmentosa or other inherited blindness today…”

Developing treatments is challenging for scientists, as more than 4,000 different gene mutations cause these conditions. But many of these mutations have something in common—a propensity for creating misfolded proteins that cells in the eye can’t process. These proteins build up inside cells, killing them from the inside out.

The new approach could potentially find use in preventing cell death in other neurodegenerative diseases, such as Huntington’s, Parkinson’s, and Alzheimer’s, says Vadim Arshavsky, senior author of the new study and professor of ophthalmology at the Duke University School of Medicine.

“You can offer almost nothing in terms of treatment to a patient with retinitis pigmentosa or other inherited blindness today,” Arshavsky says. “This investigation provides evidence that enhancing the capacity of the cell to process misfolded proteins is worth pursuing. Another important piece is that inherited blindness is just a subset of a larger category of neurodegenerative diseases, so this concept could be tested in other conditions, as well.”

The Duke research team collaborated with colleagues from the California Institute of Technology. They focused on the proteasome: machinery inside all cells that eliminates misfolded proteins. Arshavsky compares the barrel-shaped structure to a paper shredder, with the cutting elements hidden inside.

Misfolded proteins must pass through a “lid” on the shredder to be processed, but cells in diseased mice do not have enough lids, enabling the buildup of the damaged proteins.

Instead of trying to alter the shredders, Arshavsky and his team genetically increased the quantities of lids for the shredders, allowing cells to process more misfolded proteins.

In trials, mice with added proteasome lids retained four times the number of functional retinal cells by adulthood than mice with the same form of retinitis pigmentosa, which went blind as adults.

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The researchers introduced the lids genetically in the line of lab mice. In humans, scientists could potentially add lids through gene therapy or drug compounds.

“If you can retain four times the number of the functional cells in the eye, that would mean decades more vision in a human patient,” Arshavsky says. “It’s not a complete cure, but it’s a tremendous delay. This type of treatment has the potential to defer the onset of blindness beyond the human lifespan.”

The researchers report their findings in the journal Nature Communications.

The National Institutes of Health, Duke University, Research to Prevent Blindness Inc., the Knights Templar Eye Foundation, the Howard Hughes Medical Institute, and Amgen supported the research. The authors declared no competing interests related to this research.

Source: Duke University

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