It may be possible to restore at least some visual function in people blinded by optic nerve damage from glaucoma, estimated to affect more than 4 million Americans, or from trauma, suggests research from Boston Children’s Hospital.
The scientists restored vision in mice with optic nerve injury by using gene therapy to get the nerves to regenerate and, the crucial step, adding a channel-blocking drug to help the nerves conduct impulses from the eye to the brain. In the future, they believe, the same effect could be achieved with drugs alone.
In the study, previously blind mice turned their heads to follow patterns of moving bars after given the treatment, say co-senior investigators Zhigang He, PhD, and Michela Fagiolini, PhD, of the Department of Neurology and F.M. Kirby Neurobiology Center at Boston Children’s. The technicians doing the tests did not know which mice had been treated.
“By making the bars thinner and thinner, we found that the animals could not only see, but they improved significantly in how well they could see,” says Fagiolini.
While other teams, including one at Boston Children’s, have restored partial vision in mice, they relied on genetic techniques that can only be done in a lab. Generally, their methods involved deleting or blocking tumor suppressor genes, which encourages regeneration but could also promote cancer.
The new study is the first to restore vision with an approach that could realistically be used in the clinic, and that does not interfere with tumor suppressor genes.
Getting Nerves to Conduct
The key advance in restoring vision was getting the regenerated nerve fibers (axons) to not only form working connections with brain cells, but also to carry impulses (action potentials) all the way from the eye to the brain.
The challenge was that the fibers regrow without the insulating sheath known as myelin, which helps propagate nerve signals over long distances.
“We found that the regenerated axons are not myelinated and have very poor conduction—the travel speed is not high enough to support vision,” says He. “We needed some way to overcome this issue."
Turning to the medical literature, they learned that a potassium channel blocker, 4-aminopyridine (4-AP), helps strengthen nerve signals when myelin is absent.
The drug is marketed as AMPYRA for multiple sclerosis, which also involves a loss of myelin. When they added it, the signals were able to go the distance.
Paradigm for Treating Glaucoma and Optic Nerve Injury
While the study used a gene therapy virus called AAV to deliver the growth factors that trigger regeneration (osteopontin, insulin-like growth factor 1 and ciliary neurotrophic factor), He and Fagiolini are testing whether injecting a “cocktail” of growth factor proteins directly into the eye could be equally effective.
“We’re trying to better understand the mechanisms and how often the proteins would have to be injected,” says He. “The gene therapy virus we used is approved for clinical study in eye disease, but a medication would be even better."
With regeneration kick-started, 4-AP or a similar drug could then be given systemically to maintain nerve conduction. Because 4-AP has potential side effects including seizures if given chronically, He and Fagiolini have begun testing derivatives (not yet FDA-approved) that are potentially safer for long-term use.
The researchers are further testing the mice to better understand the extent of visual recovery and whether their approach might get myelin to regrow over time.
“The drugs might need to be paired with visual training to facilitate recovery,” says Fagiolini. “But now we have a paradigm to push forward."
Fengfeng Bei, Henry Hing Cheong Lee, Xuefeng Liu, Georgia Gunner, Hai Jin, Long Ma, Chen Wang, lijun Hou, and others Restoration of Visual Function by Enhancing Conduction in Regenerated Axons Cell, Vol. 164, Issues 1-2, p219–232
Illustration: The white areas in this image show extensive regeneration of nerve fibers (axons) in the central nervous system achieved by gene therapy after optic nerve injury. (The blue areas indicate scar tissue.) By adding a potassium channel blocking drug to this treatment, He, Fagiolini and colleagues were able to boost conduction in the regenerated nerves and thereby restore visual function. Credit: Fengfeng Bei, PhD