Stem cell-based screen identifies potential new treatments

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Vision loss related to aging or inherited genetic disease, such as age-related macular degeneration and retinitis pigmentosa (RP), respectively, is estimated to impact 16 million people worldwide and is often caused by defects in the retinal pigment epithelium (RPE) in the eye. The RPE is charged with clearing waste products arising during the normal visual process when light meets the photoreceptor cells in the eye through a process called phagocytosis. Failure to clear and recycle these waste products through phagocytosis eventually leads to photoreceptor cell death and vision loss.

In a recent study published in Stem Cell Reports, Seba Almedawar, Ph.D., and colleagues with the Center for Regenerative Therapies TU Dresden, Germany, used induced (iPSCs) derived from the skin of healthy donors and of patients with retinitis pigmentosa to find drugs with the potential to enhance RPE phagocytosis. The iPSCs, which can be reprogrammed into any type of cell, were converted into RPE cells and then used in a high-throughput screen (an automated process that makes it possible to achieve large scale repetition of an experiment) of 1,600 FDA approved drugs. As a result, the researchers were able to identify several drugs that enhanced phagocytosis in the RPE cultures. One drug tested, the antibiotic Ramoplanin, rescued phagocytosis defects in RPE from patients with a certain genetic form of RP.

Further studies will be required to test if this drug enhances phagocytosis in animal models of RP and if successful, ultimately human patients. Additional screening of much larger libraries may also reveal additional compounds with potential to treat these diseases that result in blindness.

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More information: Stem Cell Reports (2020). DOI: 10.1016/j.stemcr.2020.10.013 ,
Journal information: Stem Cell Reports

Provided by International Society for Stem Cell Research
Citation: Stem cell-based screen identifies potential new treatments (2020, November 25) retrieved 4 October 2022 from
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