The identification of small molecules that stimulate retinal pigment epithelial cells: potential novel therapeutic options for treating retinopathies
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem, přehledy
Odkazy
PubMed
30616395
DOI
10.1080/17460441.2019.1559148
Knihovny.cz E-zdroje
- Klíčová slova
- AMD, Hipscs, RPE differentiation, cell therapy, retinal dystrophies, retinal pigment epithelial cells, small molecules,
- MeSH
- buněčná diferenciace fyziologie MeSH
- kombinovaná terapie MeSH
- lidé MeSH
- makulární degenerace patofyziologie terapie MeSH
- nemoci retiny patofyziologie terapie MeSH
- pluripotentní kmenové buňky cytologie MeSH
- retinální pigmentový epitel cytologie MeSH
- rychlé screeningové testy MeSH
- transplantace kmenových buněk metody MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
Combinatory strategies using pharmacology and stem cell therapy have emerged due to their potential in the treatment of retinal pigment epithelium (RPE) cell related diseases, and a variety of different stem cell sources have been evaluated both in animal models and in humans. RPE cells derived from human embryonic stem cells (hESCs) and human induced pluripotent cells (hiPSCs) are already in clinical trials, holding great promise for the treatment of age-related macular disease (AMD) and hereditary RPE-related retinal dystrophies. Highly efficient protocol for RPE generations have been developed, but they are still time-consuming and laborious. Areas covered: The authors review RPE related diseases, as well as the known functions of RPE cells in retinal homeostasis. The authors also discuss small molecules that target RPE in vivo as well as in vitro to aid RPE differentiation from pluripotent stem cells clinically. The authors base this review on literature searches performed through PubMed. Expert opinion: Using high-throughput systems, technology will provide the possibility of identifying and optimizing molecules/drugs that could lead to faster and simpler protocols for RPE differentiation. This could be crucial in moving forward to create safer and more efficient RPE-based personalized therapies.