Breakthrough cell therapy to improve memory following traumatic brain injury
Researchers have developed a breakthrough cell therapy to improve memory and prevent seizures in mice following traumatic brain injury.
The study — ‘Transplanted interneurons improve memory precision after traumatic brain injury’ — was published in the journal of ‘Nature Communications.’
Traumatic brain injuries (TBI) affect two million Americans each year and cause cell death and inflammation in the brain. People, who experience a head injury often, suffer from lifelong memory loss and can develop epilepsy.
In the study, the team transplanted embryonic progenitor cells capable of generating inhibitory interneurons, a specific type of nerve cell that controls the activity of brain circuits, into the brains of mice with traumatic brain injury. They targeted the hippocampus, a brain region responsible for learning and memory.
The researchers have discovered that the transplanted neurons migrated into the injury where they formed new connections with the injured brain cells and thrived long term.
Within a month after treatment, the mice showed signs of memory improvement such as being able to tell the difference between a box where they had an unpleasant experience from one where they did not.
They were able to do this just as well as mice that never had a brain injury. The cell transplants also prevented the mice from developing epilepsy, which affected more than half of the mice who were not treated with new interneurons.
“Inhibitory neurons are critically involved in many aspects of memory, and they are extremely vulnerable to dying after a brain injury,” said Robert Hunt, PhD, assistant professor of anatomy and neurobiology at UCI School of Medicine, who led the study.
“While we cannot stop interneurons from dying, it was exciting to find that we can replace them and rebuild their circuits,” added Hunt.
To further test their observations, Hunt and his team silenced the transplanted neurons with a drug, which caused the memory problems to return.
“It was exciting to see the animals’ memory problems come back after we silenced the transplanted cells because it showed that the new neurons really were the reason for the memory improvement,” said Bingyao Zhu, a junior specialist and first author of the study.
Currently, there are no treatments for people who experience a head injury. If the results in mice can be replicated in humans, it could have a tremendous impact on patients. The next step is to create interneurons from human stem cells.
“So far, nobody has been able to convincingly create the same types of interneurons from human pluripotent stem cells,” Hunt said. “But I think we’re close to being able to do this.
The study — ‘Transplanted interneurons improve memory precision after traumatic brain injury’ — was published in the journal of ‘Nature Communications.’
Traumatic brain injuries (TBI) affect two million Americans each year and cause cell death and inflammation in the brain. People, who experience a head injury often, suffer from lifelong memory loss and can develop epilepsy.
In the study, the team transplanted embryonic progenitor cells capable of generating inhibitory interneurons, a specific type of nerve cell that controls the activity of brain circuits, into the brains of mice with traumatic brain injury. They targeted the hippocampus, a brain region responsible for learning and memory.
The researchers have discovered that the transplanted neurons migrated into the injury where they formed new connections with the injured brain cells and thrived long term.
Within a month after treatment, the mice showed signs of memory improvement such as being able to tell the difference between a box where they had an unpleasant experience from one where they did not.
They were able to do this just as well as mice that never had a brain injury. The cell transplants also prevented the mice from developing epilepsy, which affected more than half of the mice who were not treated with new interneurons.
“Inhibitory neurons are critically involved in many aspects of memory, and they are extremely vulnerable to dying after a brain injury,” said Robert Hunt, PhD, assistant professor of anatomy and neurobiology at UCI School of Medicine, who led the study.
“While we cannot stop interneurons from dying, it was exciting to find that we can replace them and rebuild their circuits,” added Hunt.
To further test their observations, Hunt and his team silenced the transplanted neurons with a drug, which caused the memory problems to return.
“It was exciting to see the animals’ memory problems come back after we silenced the transplanted cells because it showed that the new neurons really were the reason for the memory improvement,” said Bingyao Zhu, a junior specialist and first author of the study.
Currently, there are no treatments for people who experience a head injury. If the results in mice can be replicated in humans, it could have a tremendous impact on patients. The next step is to create interneurons from human stem cells.
“So far, nobody has been able to convincingly create the same types of interneurons from human pluripotent stem cells,” Hunt said. “But I think we’re close to being able to do this.