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Writer's pictureKen Ecott

Axolotl salamanders could provide key to human spinal cord regeneration


Gene partnerships found in Axolotls could give insights into how spinal cord injuries and neurodegenerative conditions could be better treated

Researchers are one step closer to solving the mystery of why some vertebrates can regenerate their spinal cords while others, including humans, create scar tissue after spinal cord injury, leading to lifelong damage.

To begin thinking about how to accomplish human spinal cord regeneration, scientists have taken note of animals that already show this ability. A prime example is the axolotl (Ambystoma mexicanum), a species of aquatic salamander. Unlike humans, it has the “superpower” of regenerating its limbs, spinal cord, heart, and other organs.

Scientists at the Marine Biological Laboratory have identified gene “partners” in the axolotl salamander that, when activated, allow the neural tube and associated nerve fibers to functionally regenerate after severe spinal cord damage. Interestingly, these genes are also present in humans, though they are activated in a different manner. Their results were recently published this Nature Communications Biology.

“[Axolotls are] the champions of regeneration, in that they can regenerate multiple body parts. For example, if you make a lesion in the spinal cord, they can fully regenerate it and gain back both motor and sensory control,” said Karen Echeverri, associate scientist in the Eugene Bell Center for Regenerative Biology and Tissue Engineering at the UChicago-affiliated MBL. “We wanted to understand what is different at a molecular level that drives them towards this pro-regenerative response instead of forming scar tissue.”

Echeverri’s prior research had shown that, in both axolotls and humans, the c-Fos gene is up-regulated in the glial cells of the nervous system after spinal cord injury. She also knew that c-Fos cannot act alone.

“c-Fos has a different partner in axolotl than it has in humans and this seems to drive a completely different response to injury,” Echeverri said.

In human injury response, c-Fos is paired with the gene c-Jun. In axolotls, however, Echeverri and her team determined that c-Fos is activated with the gene JunB. This difference in gene activation was traced to the actions of microRNAs, which regulate gene expression.

Upregulation of miR-200a in glial cells after spinal cord injury is required for spinal cord regeneration. a qRT-PCR analysis shows that miR-200a is upregulated at 3 days post injury (n = 3). b In situ hybridization confirms miR-200a expression specifically in glial cells at 3 days post injury in the regenerating spinal cord.

 

By modifying gene expression by the axolotls’ microRNA, they were able to force the human pairing of c-Fos with c-Jun. The salamanders with the human pairings were unable to regain a functioning spinal cord after injury, instead forming the scar tissue that occurs in human injury repair. Follow-up studies will investigate if the reverse is true in human cells.

Understanding the axolotl spinal cord regeneration and its differences from—and, more interestingly, similarities to—the human process could help researchers and eventually doctors improve treatment for severe human spinal cord injuries.

“That has a huge translation potential, not just for spinal cord injury in humans, but also for a lot of neurodegenerative diseases,” she said.

The Marine Biological Laboratory is dedicated to scientific discovery—exploring fundamental biology, understanding marine biodiversity and the environment, and informing the human condition through research and education. Founded in Woods Hole, Massachusetts in 1888, the MBL is a private, nonprofit institution and an affiliate of the University of Chicago.

“The genes involved in regeneration in axolotl are highly conserved between humans and axolotls, and it doesn’t appear so far that axolotls have regeneration-specific genes,” Echeverri said. “It’s all about who you partner with directly after injury, and how that drives you toward either regeneration or forming scar tissue. It’s kind of like in life: Who you partner with can have a really positive or negative effect.”

 

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