Scar-forming cells called astrocytes play a key role in repair and regrowth following spinal cord injury, says a new mouse study. It was thought that astrocytes were responsible for blocking neuronal regrowth across the level of spinal cord injury.
"At first, we were completely surprised when our early studies revealed that blocking scar formation after injury resulted in worse outcomes. Once we began looking specifically at regrowth, though, we became convinced that scars may actually be beneficial," said Michael V. Sofroniew, M.D., Ph.D., professor of neurobiology at the University of California, Los Angeles, and senior author of the study. "Our results suggest that scars may be a bridge and not a barrier towards developing better treatments for paralyzing spinal cord injuries."
‘Scar-forming cells called astrocytes have immediate benefits by decreasing inflammation at the injury site and preventing the spread of tissue damage.’
Neurons communicate with one another by sending messages down long extensions called axons. When axons in the brain or spinal cord are severed, they do not grow back automatically. For example, damaged axons in the spinal cord can result in paralysis. When an injury occurs, astrocytes become activated and go to the injury site, along with cells from the immune system and form a scar. However, long-term effects of the scars were thought to interfere with axon regrowth.
Using three different mouse models to examine the effect of astrocyte scars on axonal regrowth, Dr. Sofroniew's team was able to remove the scars or prevent them from forming after a spinal cord injury. The results revealed that without astrocyte scars, there was no regrowth.
In another experiment of spinal cord injury in mice, Dr. Sofroniew's team shuttled growth factors, specific molecules that stimulate axons to grow, to the injury site and discovered that there was robust regrowth through astrocyte scars. However, if the researchers prevented scar formation, the regrowth was significantly reduced.
Genetic analyzes revealed that astrocytes as well as non-astrocyte cells released a variety of chemicals involved in regrowth at the injury site. In this mix, Dr. Sofroniew and his colleagues found molecules that block regrowth along with molecules that support it.
"This important research provides further evidence about the complexity of the brain and spinal cord's injury response. It shows that scar-forming astrocytes support axon growth and suggests that therapeutics directed only at blocking these cells may not enhance regeneration of the injured spinal cord," said Lyn Jakeman, Ph.D., program director at the NIH's National Institute of Neurological Disorders and Stroke (NINDS), which provided funding for the study.
Trauma leads to spinal cord injury in about 12,500 people in the U.S. each year. It is estimated that 276,000 individuals in the country suffer from long-term effects of spinal cord injury. The ultimate goal of spinal cord injury research is to enable connections to develop that cross the level of injury and rewire the normal cord below.
Dr. Sofroniew and his colleagues are planning to investigate the exact mechanisms by which astrocytic scars support growth and ways to increase that response. "These preliminary findings established that axonal growth can occur in the presence of scars in mice. Eventually, we would like to see the regenerating axons grow far enough into healthy tissue to establish functional connections," said Dr. Sofroniew.
The research was funded by the National Institutes of Health, and published in Nature