To help to understand how color vision develops researchers have successfully grown human retinas in a Petri dish. These bio-constructs will allow for different theories to be tested.
The work may lay the groundwork for therapies for eye diseases such as color blindness and macular degeneration. It also establishes lab-created “organoids”—artificially grown organ tissue—as a model to study human development on a cellular level.
“Everything we examine [in a retina organoid] looks like a normal developing eye, just growing in a dish,” says Robert Johnston, a developmental biologist at Johns Hopkins University. “You have a model system that you can manipulate without studying humans directly.”
The fate of stem cells
Johnston’s lab explores how a cell’s fate is determined—what happens in the womb to turn a developing stem cell into a cell with a specific function. In the retina research, he and his team focused on the development of cells that allow people to see blue, red, and green—the three cone photoreceptors in the human eye.
While most vision research is done on mice and fish, neither of those species has the dynamic daytime and color vision of humans. So Johnston’s team created the human eye tissue they needed from stem cells.
“Trichromatic color vision differentiates us from most other mammals,” says lead author Kiara Eldred, a graduate student. “Our research is really trying to figure out what pathways these cells take to give us that special color vision.”
Over months, as the cells grew in the lab and became full-blown retina tissue, the team found the blue-detecting cells materialized first, followed by the red- and green-detecting ones.
In both cases, they found, the key to the molecular switch was the ebb and flow of thyroid hormone. Importantly, the thyroid gland, which of course wasn’t in the lab dish, didn’t control the level of this hormone, but the eye tissue itself did.
Once the researchers understood how the amount of thyroid hormone dictated whether the cells became blue or red and green receptors, they could manipulate the outcome, creating retinas that—if they had been part of a complete human eye—would have seen only blue, and others that would have detected green and red.
Insight into vision
The finding that thyroid hormone is essential for creating red-green cones provides insight into why pre-term babies, who have lowered thyroid hormone levels as they are lacking the maternal supply, have a higher incidence of vision disorders.
“If we can answer what leads a cell to its terminal fate, we are closer to being able to restore color vision for people who have damaged photoreceptors,” Eldred says. “This is a really beautiful question, both visually and intellectually—what is it that allows us to see color?”
These findings are a first step for the lab. In the future, the researchers would like to use organoids to learn even more about color vision and the mechanisms involved in the creation of other regions of the retina, such as the macula. Since macular degeneration is one of the leading causes of blindness in people, understanding how to grow a new macula could lead to clinical treatments.
There’s growing optimism among scientists that new treatments for retinal diseases will emerge from such efforts, Becker says. Initially, he says, researchers had doubts about whether a retina grown in a dish could mimic the real thing.
But studies like this one on color vision, he says, “show that the similarity is quite high.”
To encourage scientists to develop more retinal organoids, the National Eye Institute is sponsoring a scientific competition with $1 million in prizes.
As well as assisting with eye research, the development can also assist wit other research, as it has established the protocol for producing laboratory-created “organoids”, which can be used as the model to study other facets of human development at the cellular level.
The new research has been published in the journal Science. The research paper is titled “Thyroid hormone signaling specifies cone subtypes in human retinal organoids.”