Preclinical model may shed light on eye disease


Researchers at Weill Cornell Medicine have developed a preclinical model of the leading cause of central vision loss in older individuals and used it to identify new treatment modalities and drug targets.

Previously created mouse models have not sufficiently mimicked the characteristics of dry age-related macular degeneration (AMD) in humans. By contrast, the new model, described in a paper published Jan. 18 in Nature Communications, demonstrates the accumulation of fatty deposits under the retina called drusen, a hallmark of the disease.

“Creating a robust model of dry AMD has been a holy grail in the field,” said senior author Ching-Hwa Sung, the Betty Neuwirth Lee and Chilly Professor in Stem Cell Research and a professor of cell biology in ophthalmology and of cell and developmental biology at Weill Cornell Medicine. “We anticipate our model will be a valuable tool for understanding the early development and progression of the disease and designing potential therapies.”

AMD is the leading cause of blindness in adults over the age of 65, affecting an estimated 196 million people worldwide in 2020 and a projected total of 288 million by 2040. More than 80% of AMD cases are dry AMD, which involves  the lesions at the central part of the retina known as the macula and the formation of drusen. Symptoms of the condition include blurry, distorted or loss of central vision. Compromised central vision can make daily life activities extremely challenging. There are currently no treatments for dry AMD.

Sung and colleagues at Weill Cornell Medicine’s Margaret M. Dyson Vision Research Institutegenetically engineered the mouse model by eliminating a gene called chloride intracellular channel 4 (CLIC4) from the retinal pigment endothelium (RPE) cells. Although CLIC4 had not been identified previously as a gene associated with a risk of AMD, the investigators found that removing CLIC4 triggered the changes of many genes associated with AMD, creating a chronic stress condition that led to the pathology mimicking the advanced form of dry AMD.

Using their model, the researchers discovered that the lipids forming drusen initially came from the retina-lining RPE cells, rather than from blood. The discovery, which represents a new treatment target for further development, may also explain why treating patients with statins that lower cholesterol levels in the blood has not been an effective approach for treating dry AMD.

The researchers are continuing to use the model to elucidate and advance understanding of dry AMD disease processes.

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