UCLA biologists have discovered how head injuries adversely affect individual cells and genes that can lead to serious brain disorders. The life scientists provide the first cell “atlas” of the hippocampus—the part of the brain that helps regulate learning and memory—when it is affected by traumatic brain injury. The team also proposes gene candidates for treating brain diseases associated with traumatic brain injury, such as Alzheimer’s disease and post-traumatic stress disorder.
The researchers studied more than 6,000 cells in 15 hippocampal cell types—the first study of individual cell types subject to brain trauma. Each cell has the same DNA, but which genes are activated varies among different cell types. Among the 15 cell types are two that were previously unknown, each with a unique set of active genes.
“Every cell type is different,” said Fernando Gomez-Pinilla, a UCLA professor of neurosurgery and of integrative biology and physiology, and co-senior author of the study, which was published in the journal Nature Communications.
The biologists found that hundreds of genes are adversely affected by mild traumatic brain injury, such as a concussion. These altered genes can later lead to Alzheimer’s, Parkinson’s and other diseases.
The researchers reproduced a concussion-like brain injury in mice, and studied other mice that did not receive a brain injury. The researchers analyzed thousands of cells in the hippocampus of both groups of mice. Among their findings:
- The mice without an injury had very low levels in 14 of the 15 cell types of a gene called Ttr that regulates metabolism, controls thyroid hormones and performs other functions. Brain trauma increased the level of Ttr in essentially all of the cell types, the researchers found. They concluded Ttr is important to brain health and may function to bring more thyroid hormone to the brain to maintain metabolism. A thyroid hormone called T4 was injected in mice. T4 improved traumatic brain injury-induced learning deficits and reversed changes in 93 genes that affect learning and memory. This reversal in damage caused by traumatic brain injury is a major new finding. After brain injury, metabolism is substantially reduced. The biologists think T4 may “reboot” metabolism.
- Researchers found evidence that at least 12 of 15 cell types are negatively affected by brain trauma, some more strongly than others.
- The researchers were able to see how genes that have been linked to Alzheimer’s disease acted within different cell types, providing new details about where these genes act when they are affected by brain trauma. “We are learning which cell types we may want to target in future research,” said Xia Yang, a senior author of the study and a UCLA associate professor of integrative biology and physiology. “Maybe Alzheimer’s disease-related genes do not have to be active in all different cell types.”
- For the first time, the biologists found several genes that are affected by traumatic brain injury, which has recently been linked to neurotic behavior in humans. Traumatic brain injury has been associated with depression, anxiety and schizophrenia. This research could lead to new treatments for these conditions.
- Injury to the brain can lead to what is known as post-traumatic epilepsy. The researchers found a gene that could serve as a potential target for treating this kind of epilepsy.
- Traumatic brain injury causes changes in how cells communicate with one another (see attached image).
“Knowing which genes in which cells are changing in a particular person can lead to the right treatment for that person,” said Yang, who is a member of UCLA’s Institute for Quantitative and Computational Biology.
Gomez-Pinilla, who also is a member of UCLA’s Brain Injury Research Center, describes the new research as an advance in precision medicine, which holds the promise of individualized treatments for diseases.
More information: Douglas Arneson et al, Single cell molecular alterations reveal target cells and pathways of concussive brain injury, Nature Communications (2018). DOI: 10.1038/s41467-018-06222-0