Long-Term Transplant Effects of iPSC-RPE Monolayer in Immunodeficient RCS Rats
Autor: | Biju B. Thomas, Juan Carlos Martinez Camarillo, Mark S. Humayun, David Hinton, Danhong Zhu, Ruchi Sharma, Kapil Bharti, Deepthi S. Rajendran Nair |
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Rok vydání: | 2021 |
Předmět: |
Retinal degeneration
Pathology medicine.medical_specialty Superior Colliculi Light QH301-705.5 Polymers Induced Pluripotent Stem Cells retinal pigment epithelium Cell fate determination Xylenes retinal transplantation Article Implants Experimental Fibrosis medicine Animals Humans Biology (General) Induced pluripotent stem cell Vision Ocular Retinal pigment epithelium business.industry immunodeficient RCS rat Mesenchymal stem cell Parylene C General Medicine Macular degeneration medicine.disease ultrathin parylene Survival Analysis eye diseases Rats cell_developmental_biology medicine.anatomical_structure retinal degeneration sense organs business iPSC-RPE Biomarkers |
Zdroj: | Cells Cells, Vol 10, Iss 2951, p 2951 (2021) Volume 10 Issue 11 |
ISSN: | 2073-4409 |
Popis: | Retinal pigment epithelium (RPE) replacement therapy is evolving as a feasible approach to treat age-related macular degeneration (AMD). In many preclinical studies, RPE cells are transplanted as a cell suspension into immunosuppressed animal eyes and transplant effects have been monitored only short-term. We investigated the long-term effects of human Induced pluripotent stem-cell-derived RPE (iPSC-RPE) transplants in an immunodeficient Royal College of Surgeons (RCS) rat model, in which RPE dysfunction led to photoreceptor degeneration. iPSC-RPE cultured as a polarized monolayer on a nanoengineered ultrathin parylene C scaffold was transplanted into the subretinal space of 28-day-old immunodeficient RCS rat pups and evaluated after 1, 4, and 11 months. Assessment at early time points showed good iPSC-RPE survival. The transplants remained as a monolayer, expressed RPE-specific markers, performed phagocytic function, and contributed to vision preservation. At 11-months post-implantation, RPE survival was observed in only 50% of the eyes that were concomitant with vision preservation. Loss of RPE monolayer characteristics at the 11-month time point was associated with peri-membrane fibrosis, immune reaction through the activation of macrophages (CD 68 expression), and the transition of cell fate (expression of mesenchymal markers). The overall study outcome supports the therapeutic potential of RPE grafts despite the loss of some transplant benefits during long-term observations. |
Databáze: | OpenAIRE |
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