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.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-11-03
DOI
https://doi.org/10.64898/2026.10.28.761748
Primary Topic
Retinal Development and Disorders
Type
preprint
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preprint

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

Eeshika Mitra, Daniel M. Lipinski, Phyllis Summerfelt, Kenneth P. Allen et al.
bioRxiv (Cold Spring Harbor Laboratory)
Retinal Development and Disorders
preprint

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

Eeshika Mitra, Daniel M. Lipinski, Phyllis Summerfelt, Kenneth P. Allen, Susan Freling, Joseph Carroll, Sangeetha Kandoi, Hannah M. Follett, Deepak A. Lamba, Ching Tzu Yu, Ramesh Periasamy
preprint en

Abstract

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.

bioRxiv (Cold Spring Harbor Laboratory)
Johns Hopkins University (US), University of California, San Francisco (US), Genentech (US), Medical College of Wisconsin (US), Max Planck Florida Institute for Neuroscience (US)
Retinal Development and Disorders
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