Scaffold-Free Retinal Pigment Epithelium Microtissues Exhibit Increased Release of PEDF
Autor: | Kayla Giles, Mark Ungrin, Saud Sunba, Abdullah Al-Ani, Derek Toms, Yacine Touahri, Carol Schuurmans |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
retina
QH301-705.5 Human Embryonic Stem Cells Retinal Pigment Epithelium Biology Catalysis Article Cell Line Inorganic Chemistry chemistry.chemical_compound Macular Degeneration PEDF Tissue engineering medicine Cell Adhesion Humans Nerve Growth Factors Biology (General) Physical and Theoretical Chemistry Eye Proteins QD1-999 Molecular Biology Spectroscopy Cells Cultured Serpins Retina Retinal pigment epithelium Choroid Organic Chemistry Retinal General Medicine Macular degeneration medicine.disease eye diseases ESC-RPE Computer Science Applications Cell biology Transplantation Stargardt disease Chemistry ophthalmology medicine.anatomical_structure chemistry tissue engineering microtissue sense organs RPE ARPE-19 |
Zdroj: | International Journal of Molecular Sciences Volume 22 Issue 21 International Journal of Molecular Sciences, Vol 22, Iss 11317, p 11317 (2021) |
ISSN: | 1422-0067 |
Popis: | The retinal pigmented epithelium (RPE) plays a critical role in photoreceptor survival and function. RPE deficits are implicated in a wide range of diseases that result in vision loss, including age-related macular degeneration (AMD) and Stargardt disease, affecting millions worldwide. Subretinal delivery of RPE cells is considered a promising avenue for treatment, and encouraging results from animal trials have supported recent progression into the clinic. However, the limited survival and engraftment of transplanted RPE cells delivered as a suspension continues to be a major challenge. While RPE delivery as epithelial sheets exhibits improved outcomes, this comes at the price of increased complexity at both the production and transplant stages. In order to combine the benefits of both approaches, we have developed size-controlled, scaffold-free RPE microtissues (RPE-µTs) that are suitable for scalable production and delivery via injection. RPE-µTs retain key RPE molecular markers, and interestingly, in comparison to conventional monolayer cultures, they show significant increases in the transcription and secretion of pigment-epithelium-derived factor (PEDF), which is a key trophic factor known to enhance the survival and function of photoreceptors. Furthermore, these microtissues readily spread in vitro on a substrate analogous to Bruch’s membrane, suggesting that RPE-µTs may collapse into a sheet upon transplantation. We anticipate that this approach may provide an alternative cell delivery system to improve the survival and integration of RPE transplants, while also retaining the benefits of low complexity in production and delivery. |
Databáze: | OpenAIRE |
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