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Periasamy, R.

Publications and source records attributed to Periasamy, R..

2 recordsLinked to original sources

Transplantation of human iPSC-derived retinal cells in the cone-dominant Northern tree shrew

Abstract: Purpose: To characterize the transplantation and survival of photoreceptors generated from human induced pluripotent stem cell (hiPSC)-derived retinal organoids in the Northern tree shrew (Tupaia belangeri, TS). Methods: TS eyes were injected with retinal cells dissociated from GFP-expressing hiPSC-derived retinal organoids (12 animals; n=22 eyes). 15 eyes had prior damage induced by either experimental retinal detachment (n=11) or ATP-induced retinal damage (n=4), and seven eyes were undamaged. Retinal organoids were treated with Notch pathway inhibitor 2 days before transplant. TS retinal structure and cellular details were assessed post-transplantation for up to 8 weeks using scanning laser ophthalmoscopy (SLO), optical coherence tomography (OCT), and adaptive optics SLO (AOSLO). Histological analysis was done at the end of the experiment. Results: Cell transplants in eyes treated with a simple immunosuppression treatment failed to survive for more than 2 weeks (n=10 eyes). Robust cell survival was observed in the eyes treated with a complex immunosuppression cocktail for up to 8 weeks (n=12 eyes). The transplanted cells were confirmed to be subretinally located using OCT imaging and the cell fate was confirmed to be human photoreceptors by histology. Finally, AOSLO imaging captured structures resembling photoreceptor inner segments. Conclusions: Our results demonstrate survival of transplanted cells using a species-specific immunosuppression treatment. Future studies should aim to explore the long-term survival and function of the transplanted cells.

neuroscience↗

Improving retinal vascular endothelial cell tropism through rational rAAV capsid design

Vascular endothelial cells (VEC) are essential for retinal homeostasis and their dysfunction underlies pathogenesis in diabetic retinopathy (DR) and exudative age-related macular degeneration (AMD). Studies have shown that recombinant adeno-associated virus (rAAV) vectors are effective at delivering new genetic material to neural and glial cells within the retina, but targeting VECs remains challenging. To overcome this limitation, herein we developed rAAV capsid mutant vectors with improved tropism towards retinal VEC. rAAV2/2, 2/2[QuadYF-TV], and rAAV2/9 serotype vectors (n=9, capsid mutants per serotype) expressing GFP were generated by inserting heptameric peptides (7AA) designed to increase endothelial targeting at positions 588 (2/2 and 2/2[QuadYF-TV] or 589 (2/9) of the virus protein (VP 1-3). The packaging and transduction efficiency of the vectors were assessed in HEK293T and bovine VECs using Fluorescence microscopy and flow cytometry, leading to the identification of one mutant, termed EC5, that showed improved endothelial tropism when inserted into all three capsid serotypes. Intra-ocular and intravenous administration of EC5 mutants in C57Bl/6j mice demonstrated moderately improved transduction of the retinal vasculature, particularly surrounding the optic nerve head, and evidence of sinusoidal endothelial cell transduction in the liver. Most notably, intravenous administration of the rAAV2/2[QuadYF-TV] EC5 mutant led to a dramatic and unexpected increase in cardiac muscle transduction.

molecular biology↗