Spinal Cord Repair: Cellular Bridges for Healing
- A new study indicates that manipulating cells within blood vessels could offer a novel approach to spinal cord injury repair.
- Scientists introduced a recombinant protein to the injury site, where pericytes had gathered.
- Mice treated with a single injection of the growth-factor protein experienced axon regrowth and regained some movement in their hind limbs.
Discover a breakthrough in spinal cord injury repair: A new study reveals that a protein, PDGF-BB, can stimulate cellular bridges, leading to axon regeneration. Researchers observed that this innovative approach, which involves manipulating cells within blood vessels, promoted significant axon regrowth and improved motor function in mice. This innovative therapy utilizes pericytes, and the formation of cellular bridges to support nerve cell extensions. Scientists at The Ohio State University College of Medicine injected a growth-factor protein, leading to increased axon growth. Initial results suggest the potential broader impact and could offer new avenues. This work, published by News Directory 3, might extend to brain injury and stroke. Explore how restoring blood flow holds the key. Discover what’s next …
Protein Shows Promise in Spinal cord Injury Repair
Updated June 23, 2025
A new study indicates that manipulating cells within blood vessels could offer a novel approach to spinal cord injury repair. The research, primarily conducted on mice, focused on pericytes, cells found in the smallest blood vessels.
Scientists introduced a recombinant protein to the injury site, where pericytes had gathered. The protein prompted the pericytes to change shape and alter their molecular production, effectively creating “cellular bridges.” These bridges then supported the regeneration of axons, the nerve cell extensions responsible for transmitting signals.
Mice treated with a single injection of the growth-factor protein experienced axon regrowth and regained some movement in their hind limbs. Further experiments with human cells suggest these findings may not be limited to mice.
Andrea Tedeschi, associate professor of neuroscience at The Ohio State University College of Medicine and senior author of the study, expressed surprise at the treatment’s effectiveness. “There’s a lot more that can be learned and a lot that can be expanded, but the more we worked on this, the more stunned we really were by the potency of this single treatment and how effective it was,” Tedeschi said.She added that the implications extend beyond spinal cord injury, perhaps impacting brain injury, stroke, and neurodegenerative diseases.
The research highlights the critical role of blood vessel restoration in neurological recovery following spinal cord injuries.
Wenjing Sun, assistant professor of neuroscience at Ohio State and the study’s first author, emphasized the importance of vascular health. “Spinal cord injuries are severe not only as they prevent transmission of information across the site of the injury, but because all of the vasculature structure and function is also compromised,” Sun said. “Even if you are able to reestablish neuronal connectivity from one end to the other, the overall effect will still not be maximized unless you take care of everything else that falls apart.”
The study, published in molecular Therapy on April 18, explored the protein platelet-derived growth factor BB (PDGF-BB). While previous research suggested pericytes might hinder spinal cord injury recovery, cancer research revealed that PDGF-BB exposure alters pericyte properties, a mechanism tumors use to generate blood supply. The team saw potential in leveraging this relationship to stabilize blood vessels around the injury.
Imaging studies confirmed that pericytes migrate to the injury site after a spinal cord is severed, but they don’t promote the growth of functional blood vessels needed for axon regeneration. In lab experiments, a “carpet” of pericytes treated with PDGF-BB substantially enhanced axon growth from mouse sensory neurons.
Tedeschi explained that the pericytes, combined with the growth factor, rearranged fibronectin, a glycoprotein crucial for tissue repair.The cells also elongated, creating structures more conducive to axon regeneration.”We certainly know these cells are going to infiltrate and deposit at the lesion epicenter. These elongated fiber structures that they become are far more permissive in promoting axons to regenerate from one end to the other and bypass the injury,” Tedeschi said.
Animal experiments involved injecting PDGF-BB seven days post-injury.Tissue analysis four weeks later showed robust axon regeneration compared to control mice. “When we looked at formation of these pericyte structures that crossed the injury site,we saw the treatment promoted the growth of these bridges. And most if not all of these regenerating axons were able to escape the injury site by riding these cellular bridges that have formed
