The researchers, co-led by Associate Professor Amy Wagers of Harvard’s Department of Stem Cell and Regenerative Biology and the Harvard Stem Cell Institute, has found that impairment of the body’s ability to replace protective myelin sheaths, which surround nerve fibers and allow them to send signals properly, may be reversible, offering new hope that therapeutic strategies aimed at restoring efficient regeneration can be effective in the central nervous system throughout life.
In a proof-of-principle study published in the journal Cell Stem Cell, the researchers report that defects in the regeneration of the myelin sheaths surrounding nerves, which are lost in diseases such as MS, may be at least partially corrected after exposing an old animal to the circulatory system of a young animal. Myelin is a fatty substance that protects nerves and aids in the quick transmission of signals between nerve cells.
In a study, researchers report that defects in the regeneration of the myelin sheaths surrounding nerves, which are lost in diseases such as MS, may be at least partially corrected after exposing an old animal to the circulatory system of a young animal. The research was led by Associate Professor Amy Wagers (above) of Harvard’s Department of Stem Cell and Regenerative Biology and the Harvard Stem Cell Institute. (B. D. Colen/Harvard University photo)
Using a surgical technique, the researchers introduced an experimental demyelinating injury in the spinal cord of an old mouse, creating small areas of myelin loss, and then exposed those areas to cells found in the blood of a young mouse. By doing so, they found that the influx of certain immune cells, called macrophages, from the young mouse helped resident stem cells restore effective remyelination in the old mouse’s spinal cord. This rejuvenating effect of young immune cells was aided in part by the greater efficiency of the young cells in clearing away myelin debris created by the demyelinating injury. Prior studies have shown that this debris impedes the regeneration of myelin.
“Aging impairs regenerative potential in the central nervous system,” said Wagers, who is based at the Joslin Diabetes Center, and who co-led the study with Professor Robin Franklin, director of the MS Society’s Cambridge Centre for Myelin Repair at the University of Cambridge. “This impairment can be reversed, however, suggesting that the eventual development of cell-based or drug-based interventions that mimic the rejuvenation signals found in our study could be used therapeutically.”
This could be particularly useful, she said, in treating MS, which typically spans many decades of life, and thus is likely to be influenced by age-dependent reductions in the ability of myelin to regenerate. In MS, the body’s own immune system attacks the myelin sheath and prevents nerve fibers in the brain from sending signals properly, which can cause mild symptoms such as limb numbness or more serious ones like losing the ability to walk or speak. As people with MS age, remyelination decreases significantly, eventually causing permanent loss of nerve fibers.
“For MS sufferers,” said Franklin, “this means that, in theory, regenerative therapies will work throughout the duration of the disease. Specifically, it means that remyelination therapies do not need to be based on stem cell transplantation, since the stem cells already present in the brain and spinal cord can be made to regenerate myelin, regardless of a person’s age.”
Other Harvard co-authors of the study were Tata Nageswara Rao and Jennifer L. Shadrach of Wagers’ lab.
—Scott Edwards, Joslin Diabetes Center Communications