Scientists Map Brain Region Linked to Alzheimer’s and Other Diseases
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USC scientists have created the most detailed atlas yet of the hippocampus, the brain’s memory bank.
Using fluorescent tracers and 3D animation, the scientists show structures, nerve connections and functions in vivid detail. The study appears today in the journal Nature Neuroscience.
“Like a new atlas, we’ve constructed the most detailed diagram of the hippocampus to date,” said Michael S. Bienkowski, lead author of the study and a researcher at the USC Mark and Mary Stevens Neuroimaging and Informatics Institute. “With a better map, we can see each region and how it functions.
“A better map is a resource scientists can use to better understand the hippocampus and how its degeneration leads to diseases.”
The human hippocampus sits at the base of the brain. It stores memories, helps regulate emotions and guides navigation by spatial processing. It’s the first part of the brain impaired by Alzheimer’s; hippocampus degeneration also can cause epilepsy and other diseases.
The research behind USC’s new brain map
In this case, scientists worked on a mouse brain because it’s organized similar to a human brain. Scientists can use the new map of the hippocampus to deliver genetically targeted drugs to specific neurons with fewer side effects, said senior author Hong-Wei Dong, USC professor of neurology and director of USC’s Center for Integrated Connectomics.
The work is part of the Mouse Connectome Project, a USC-led effort that collects data about neural connections in the brain, sharing it publicly with researchers in more than 100 countries. Disconnections in the brain underlie Huntington’s disease, Parkinson’s disease, Alzheimer’s disease, autism spectrum disorders and other illnesses.
Scientists have known the basic four-part architecture of the hippocampus for a long time. What’s different now is the USC scientists can show its sub-regions and how nerve cells interact across the structure. It’s a night-and-day difference, akin to seeing transmission lines and power poles slung across a city by day compared to fully illuminated at night. This new visualization traces neural pathways and connections in remarkable detail using fluorescent dyes as tracers that reveal cells, neuron junctions and connections to the rest of the brain.
“It totally changes our understanding by combining a wiring diagram with gene expression of the mouse hippocampus,” Bienkowski said. “We see it doing different things, and this gives us a new way to understand how the whole thing works together. This should have a very profound and broad impact.”
Alzheimer’s and dementia
Alzheimer’s disease is the sixth leading cause of death for older people and the leading cause of dementia in the United States, according to the National Institute on Aging. It accounts for 93,500 deaths nationwide annually, and the prevalence and rate of death is increasing as the population ages, according to the U.S. Centers for Disease Control and Prevention.
The Mouse Connectome Project at USC is part of a larger effort funded by the National Institutes of Health to map all the connections of the brain to understand how different structures network to regulate behavior. Dong’s research focuses on how to classify neurons based on both genetics and connectivity, information that could help other researchers develop strategies to target neurons to treat diseases in humans. The work is parallel to a Human Connectome Project, involving 100 researchers at leading research institutions with $40 million from the NIH, which maps brain connections in humans.
The human brain contains about 100 billion neurons, each with about 10,000 connections, so mapping this network is a big-data challenge involving many scientists. USC’s contribution helps advance the larger effort by starting with a simpler task such as the mouse hippocampus research.
This article has been republished from materials provided by the University of Southern California. Note: material may have been edited for length and content. For further information, please contact the cited source.