Induced pluripotent stem cells enable patient-specific disease modelling by reprogramming adult cells into pluripotent stem cells. At Narayana Netralaya Foundation, iPSC research is used to study ocular diseases at a cellular level and connect genetic findings with functional outcomes.
Many inherited retinal diseases progress silently before clinical symptoms appear. iPSC-derived retinal cells allow early disease mechanisms to be studied and therapies to be evaluated in human-relevant models.
The iPSC programme aims to:
The iPSC programme focuses on creating patient-specific cellular models to study disease mechanisms and evaluate therapeutic strategies in a controlled laboratory environment.
Core areas of focus include:
A strong emphasis is placed on translational integration, including:
Together, these efforts support a diverse portfolio of iPSC research, spanning various areas ocular and cellular dysfunction.
The iPSC programme is led by a multidisciplinary team of scientists and clinician-researchers with expertise in:
Close collaboration between laboratory researchers and clinicians ensures that research priorities remain aligned with patient needs and real-world clinical applicability.

Authors: Padmamalini Mahendradas, Aditya Patil, Rahul Patil, Raghav Narasimhan, Radhika Sriram, Sai Bhakti Mishra, Ankush Kawali, Poornachandra Gowda, Rohit Shetty, Abhijit Sinha Roy
Keywords: NA
PMID: 39561034
DOI: 10.1080/09273948.2024.2425976

Authors: Rohit Shetty, Pooja Khamar, Raghav Narasimhan, Ritika Mullick, Anushree Bhatkal, Anisha Ramesh & Abhijit Sinha Roy
Keywords: NA
PMID: 40781520
DOI: 10.1038/s41598-025-13957-6

Authors: Divyani Nayak, Shivapriya Shivakumar, Rohit Shetty, K N Prashanthi, Arkasubhra Ghosh, Nallathambi Jeyabalan, Koushik Chakrabarty
Keywords: NA
PMID: 39639354
DOI: 10.1186/s13287-024-04016-4
The iPSC programme is progressing towards: