For many years, researchers have thought that the scar that forms after a spinal cord injury actively prevents damaged neurons from regrowing. In a study of rodents, scientists showed they could overcome this barrier and reconnect severed spinal cord nerves by turning back the neurons' clocks to put them into an early growth state. Once this occurs, neurons could be induced to regrow across the scarred tissue.
"For decades researchers have been trying to make severed neurons regrow across a spinal cord injury and reconnect with neurons on the other side. This study suggests that may require manipulating three key growth processes," said the author. "These insights are important for understanding the mechanisms of injury and regeneration that may one day be applied to develop potential treatments for spinal cord injury."
Neurons send signals to each other through long projections called axons. When the spinal cord is injured, many of these axons are severed, leading to a loss of sensation and/or paralysis below the injury site. In response, a scar forms within the damaged tissue, and while the axons may briefly attempt to regrow, this process is unsuccessful. Because these connections between neurons are made initially as the body is developing, researchers have sought to restore those developmental conditions to potentially help the damaged cord heal.
"There are several growth patterns in the spinal cord that shut down after development," said the senior author of the study published in Nature. "We wanted to see if we could reactivate those patterns following injury and whether that would lead to regrowth of the axons."
Using both mouse and rat spinal cord injury models, the researchers looked at three components of the regrowth process.
First, they tried to genetically turn back the neurons' clock by reactivating the growth program that produced the original connections, specifically neurons that look like they are trying to regrow. While not active in adults, the neurons still carry the program used during early growth. By injecting viruses containing genes related to this program, the researchers were able to revert spinal cord neurons back to a state where axon growth could occur.
Second, the new axons needed to travel through the damaged tissue. Normally, growing axons move along highways paved with molecules that are not found in the scar tissue. After injecting the injury site with a gel containing a combination of growth-promoting proteins, the scientists saw an increase in axon-supportive molecules, effectively providing a "road" across the injury.
Finally, the growing axons needed to exit the injury site and find targets. During development, neurons release proteins called chemoattractants that axons home in on. To mimic this, the researchers injected chemoattractant proteins in a trail beyond the injury site and saw that these "chemical breadcrumbs" successfully led axons to grow completely through the injury site.
When any of the three treatments--viral activation of the growth program, formation of the path for axon travel, and the addition of chemoattractants--were not provided, minimal, if any regrowth was seen. In contrast, when all three were used in the order described, the neurons grew robustly. Tens or hundreds of axons traveled across the scar and reconnected with neurons on the other side.
Although their results suggest that the new connections could conduct electrical signals across the injury, the rodents could not move any better. However, the authors emphasized that this was not unexpected.
"We would expect that these regrown axons would behave very much like the new axons we see in development,"the author explained. "Much like a newborn must learn to walk, these newly formed circuits will probably require training before functional recovery can be seen."
https://www.nature.com/articles/s41586-018-0467-6
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