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Penn team characterizes the underlying cause of a form of macular degeneration

University of Pennsylvania News May 02, 2017

Best disease, also known as vitelliform macular dystrophy, affects children and young adults and can cause severe declines in central vision as patients age. The disease is one in a group of conditions known as bestrophinopathies, all linked to mutations in the BEST1 gene. This gene is expressed in the retinal pigment epithelium, or RPE, a layer of cells that undergirds and nourishes photoreceptor cells, the rods and cones responsible for vision.

Despite the century of work on bestrophinopathies and the identification of genetic mutations responsible for the conditions, no one had identified the underlying mechanism that led to the vision loss seen in Best disease until now.Using an animal model of Best disease in combination with biochemical and optical assays, a team of researchers at the University of Pennsylvania has pinpointed a number of abnormalities that give rise to the impairments seen in the disease.

“The genetic cause of the disease has been known for 20 years, but no one had samples of patients at the stage when the disease starts,” said Karina E. Guziewicz, research assistant professor of ophthalmology in Penn’s School of Veterinary Medicine and lead author on the study. "But we were now able to pinpoint this early stage and find out what factors trigger the development of lesions.”

The new information sets the team up for testing a gene therapy to treat the disease, as the researchers will be able to observe whether or not these structural and biochemical abnormalities have been corrected.

“Now that we understand what we’re seeing, it allows us to judge the success of a particular therapy,” said Gustavo D. Aguirre, professor of medical genetics and ophthalmology at Penn Vet.

Kathleen Boesze–Battaglia, a professor in the Department of Biochemistry in Penn’s School of Dental Medicine, also contributed her expertise in lipid biochemistry and spectral analysis of lipid debris to the study, which was published in the journal Progress in Retinal and Eye Research.

“Interestingly, the lipid debris accumulation is similar to cholesterol rich plaque formation, compounded by a complexity of vitamin A metabolism,” said Boesze–Battaglia. “Alterations in lipid metabolism likely contribute to the secondary disease pathology in this model.”

In this study, the Penn–led team discovered that this predilection of the macula to develop lesions has to do with differences in the supporting structures of rods versus cones.

Examining cross–sections of the fovea–like region in the canine macula of dogs affected with the canine equivalent of Best disease, the researchers found that the microvilli don’t form and that the matrix is fragmented. The susceptibility of the macula is due to the fact that cones are the predominant cell type there and rely on the matrix for support and nutrient exchange.

“We were not expecting to find such dramatic structural abnormalities,” Guziewicz said. “For a hundred years, this has been thought to be a disease of the RPE, but we have now identified this as a disease of the RPE–photoreceptor interface.”

“The RPE provides transport of nutrients to the cones and engulfs the discarded part of cones and rods,” said Aguirre. “When you lose the matrix, you lose the connection between those cells and the RPE and that leads to disease.”

To determine if the same would be true in humans, the researchers looked at human induced pluripotent stem cell–derived RPE from Best disease patients and found similar signatures: microvilli numbers were decreased in length and density.

Looking ahead, the research team would like to continue to probe the biochemical signals that lead to the improper development of the microvilli and matrix and push ahead with developing and testing a gene–therapy approach to treating bestrophinopathies.
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