AI Article Synopsis

  • - The study focuses on human Pluripotent Stem Cell (hPSC) technology, specifically using human Embryonic Stem cell derived-Retinal Pigmented Epithelial Cells (hES-RPE) for applications like cell therapy and drug screening, aiming to address eye diseases with a high socioeconomic impact.
  • - Research findings indicate that hES-RPE cells more closely mimic natural Retinal Pigmented Epithelial (RPE) cells compared to the widely used ARPE-19 cell line, showcasing superior resilience when exposed to various immunosuppressive drugs.
  • - The results suggest that hES-RPE cells could perform a wider range of RPE functions than ARPE-19, making them a promising candidate for future drug

Article Abstract

Background And Objectives: Eye diseases have a high socioeconomic impact on society and may be one of the fields in which most stem cell-related scientific accomplishments have been achieved recently. In this context, human Pluripotent Stem Cell (hPSC) technology arises as an important tool to produce and study human Embryonic Stem cell derived-Retinal Pigmented Epithelial Cells (hES-RPE) for several applications, such as cell therapy, disease modeling, and drug screening. The use of this technology in pre-clinical phases attends to the overall population desire for animal-free product development. Here, we aimed to compare hES-RPE cells with ARPE-19, one of the most commonly used retinal pigmented epithelial immortalized cell lines.

Methods And Results: Functional, cellular and molecular data obtained suggest that hES-RPE cells more closely resembles native RPEs compared to ARPE-19. Furthermore, hES-RPE revealed an interesting robustness when cultured on human Bruch's membrane explants and after exposure to Cyclosporine (CSA), Sirolimus (SRL), Tacrolimus (TAC), Leflunomide (LEF) and Teriflunomide (TER). On these conditions, hES-RPE cells were able to survive at higher drug concentrations, while ARPE-19 cell line was more susceptible to cell death.

Conclusions: Therefore, hES-RPEs seem to have the ability to incur a broader range of RPE functions than ARPE-19 and should be more thoroughly explored for drug screening.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904525PMC
http://dx.doi.org/10.15283/ijsc20094DOI Listing

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