USU Biological Engineering Professor Validates Alternative Treatments for AMD Disease
A Utah State University professor and her team has found a possible solution for treating age-related macular degeneration, one of the leading causes of vision loss for older adults.
Elizabeth Vargis is an associate professor of biological engineering whose paper was recently published in the Molecular Vision Journal on Nov. 3.
Elizabeth Vargis is an associate professor of biological engineering. Her paper was recently published in the Molecular Vision Journal on Nov. 3. Vargis’ research states that controlling the growth of retinal pigment epithelial cells, an important cell found in the eye, can explain the relationship between RPE cell detachment and blood vessel formation. RPE cells help maintain healthy vision by transporting nutrients to the parts of the eye that visualize light.
When RPE cells begin to break down, it can lead to a condition called age-related macular degeneration that causes vision loss. Current treatments target a protein called VEGF, which is responsible for abnormal blood vessel growth in the retina through a process called angiogenesis.
“While AMD treatments target VEGF to slow the angiogenesis process, there are other proteins that could contribute to AMD and could be potential targets for treatment,” Vargis said.
Vargis (right) and Ph.D. student Chase Paterson found that RPE cells could be successfully controlled by using stencil patterns, which could be a useful strategy for treating AMD.
Through the method of micropatterning, or creation of specifically patterned surfaces, Vargis and her team were able to control the arrangement of RPE cells using stencils. Patterns were formed in the stencils to mimic 10 percent, 25 percent and 50 percent detachment within an RPE cell layer. Concentrations of other proteins in the eye were also measured as potential treatments.
By using stencils to control the arrangement of RPE cells in the lab, Vargis, along with graduate student Chase Paterson and undergraduate Jamen Cannon, found that when junction proteins were disrupted, the cells secreted more of these harmful proteins.
Results showed that the growth of RPE cells was successfully controlled by the stencil patterns. When RPE cells were not held together correctly, the cells excreted levels of harmful proteins that could contribute to vision loss. Targeting those certain proteins for treatment could be a useful strategy for treating AMD, but more research will be needed to understand the timeline of their contributions to retinal diseases.
This work was supported by the National Eye Institute of the National Institutes of Health Grant R15EY028732.
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Writer: Sydney Dahle, sydney.dahle@usu.edu, 435-797-7512
Contact: Elizabeth Vargis, vargis@usu.edu, 435-797-0618