Humans and other vertebrates depend on a portion of the brain called the hippocampus for learning, memory and their sense of location. Nerve cell structures in the adult hippocampus are sustained by factors whose identities have remained largely mysterious so far.
Now, research led by a Johns Hopkins University biologist Dr. Kuruvilla sheds light on the subject, potentially pointing the way to a better understanding of how the structure of nerve cells in the adult hippocampus may deteriorate, which can lead to Alzheimer’s disease and other neurological disorders.
In a paper in the journal Proceedings of the National Academy of Sciences, Kuruvilla and eight other scientists from two research institutions report that a protein that has primarily been studied for its role in early animal development also plays a surprising role in maintaining the structure of hippocampal neurons in adult mice.
The team studied a protein called Wnt5a, which belongs to a family of proteins that have been studied primarily for their functions during embryonic development and in nurturing neurons as the young brain forms. Using mice genetically altered to remove Wnt5a from the hippocampus, the team showed that the protein’s absence did not affect hippocampus development in young mice, but instead resulted in striking degradation of specific nerve cell structures called dendrites, which resemble clusters of tree branches, in adult mice. These findings suggest that the protein plays an important role in maintaining dendrite structures as the mouse ages.
The team went further by showing that when the Wnt5a protein was reintroduced after the dendrites had started to deteriorate in aged mice, the nerve cell structures were restored – to a degree the scientists did not expect.
The team also tested the ability of mice lacking Wnt5a in the hippocampus to perform learning and memory tasks. Behavior tests were run in a Morris Water Maze designed to show how well mice use spatial cues to navigate in a water pool and how long it takes them to learn to use a hidden platform to escape. They found that mutant mice – those without Wnt5a – were poor learners and had attenuated memory; their performance in behavioral tasks became progressively worse with age.
“Together, the findings from the Morris Water Maze test support an essential role for Wnt5a in the acquisition of spatial learning and memory storage in adult animals,” the authors wrote.
In the brain, the hippocampus is the seat of short- and long-term memory and governs spatial orientation. Studies have shown that the brains of people with Alzheimer’s disease have structural alterations in dendrites, particularly in the hippocampus.
Kuruvilla said the experiments suggest avenues for further research on what may cause shrinkage of dendrites during neurological disorders. She emphasized, however, that it is premature to extrapolate these results in mice to humans.
While Kuruvilla was careful not to overstate the significance of the findings or how they may apply to cognitive disorders in humans, she said the results at least bring attention to the significance of studying molecular signals that maintain neurons in the adult brain. Compared to the wealth of information on signals that help in formation of neuronal connections in the developing brain, we know far less of how brain structure is sustained in adult life, she said.
Citation: Chih-Ming Chena, Lauren L. Oreficeb, Shu-Ling Chiuc, Tara A. LeGatesa, Samer Hattara, Richard L. Huganirc, Haiqing Zhaoa, Baoji Xub, and Rejji Kuruvillaa. “Wnt5a is essential for hippocampal dendritic maintenance and spatial learning and memory in adult mice.” PNAS 2017.
Research funding: National Institutes of Health.
Adapted from press release by Johns Hopkins University.
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