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Grants > Bioengineered Stem Cell-Derived Cone Photoreceptor Therapy Updated On: Jan. 23, 2025
Macular Degeneration Research Grant

Bioengineered Stem Cell-Derived Cone Photoreceptor Therapy

Regenerating Cells Damaged by Macular Degeneration
Derek van der Kooy, PhD

Principal Investigator

Derek Van Der Kooy, PhD

University of Toronto

Toronto, Ontario, Canada

About the Research Project

Program

Macular Degeneration Research

Award Type

Standard

Award Amount

$160,000

Active Dates

July 01, 2016 - June 30, 2018

Grant ID

M2016173

Acknowledgement

This grant is made possible in part by a bequest from the Trust of Edward Primet.

Co-Principal Investigator(s)

Brian Ballios, MD, PhD, University of Toronto

Goals

Drug therapy only slows the progression of disease, but does not represent a regenerative approach to macular degeneration treatment. We will use cell regenerative techniques to produce large quantities of cone photoreceptors for transplantation directly into the retina. Cones are the cells responsible for high-resolution/color vision and are lost in disease. We will take advantage of natural biomaterials as vehicles to deliver cells to the eye, increase their survival, and improve their function after transplantation.

Summary

We are focused on the goal of producing large quantities of cone photoreceptors for transplantation directly into the retina. Cones are the cells responsible for high-resolution/color vision and are lost in AMD.

Our first aim is to use regenerative techniques to derive cells that behave like the stem cells that grow in human eyes (“retinal stem cells”). We will treat these mass-produced retinal stem cells with specific chemical factors to produce cone photoreceptors with high purity and high efficiency. We will investigate the biological mechanisms at play during this process to better understand how to produce these therapeutically important cells. In the second phase of our project, we will take advantage of natural biomaterials as vehicles to deliver cells to the eye. In doing so, we will look to increase their survival and improve retinal function after transplantation.

We foresee that, given the state of the stem cell field, early success and key findings from this project are poised to shift the paradigm of therapeutic cell sources for the treatment of AMD toward the targeted production of specific, clinically relevant cell types to replace those lost in disease. From a clinical perspective, improved stem cell-derived cone transplantation will show that the adult retina can be repopulated with transplanted photoreceptors, and can be a viable approach to treat patients suffering from AMD.