In a study supported by the National Institutes of Health (NIH), researchers revealed the structural underpinnings of memory formation across a broad network of neurons in the mouse brain. This work sheds light on the fundamentally flexible nature of how memories are made, detailing learning-related changes at the cellular and subcellular levels with unprecedented resolution. Understanding this flexibility may help explain why memory and learning processes sometimes go awry.
The findings, published in Science, showed that neurons assigned to a memory trace reorganized their connections to other neurons through an atypical type of connection called a multi-synaptic bouton. In a multi-synaptic bouton, the axon of the neuron relaying the signal with information contacts multiple neurons that receive the signal. According to the researchers, multi-synaptic boutons may enable the cellular flexibility of information coding observed in previous research.
The researchers also found that neurons involved in memory formation were not preferentially connected with each other. This finding challenges the idea that "neurons that fire together wire together," as would be predicted by a traditional theory of learning.
In addition, the researchers observed that neurons allocated to a memory trace reorganized certain intracellular structures that provide energy and support communication and plasticity in neuronal connections. These neurons also had enhanced interactions with support cells known as astrocytes.
Using a combination of advanced genetic tools, 3D electron microscopy, and artificial intelligence, Scripps Research scientists Marco Uytiepo, Anton Maximov, Ph.D., and colleagues reconstructed a wiring diagram of neurons involved in learning and identified structural changes to these neurons and their connections at the cellular and subcellular levels.
To examine structural features associated with learning, the researchers exposed mice to a conditioning task and examined the hippocampus region of the brain about 1 week later. They selected this time point because it occurs after memories are first encoded but before they are reorganized for long-term storage. Using advanced genetic techniques, the researchers permanently labeled subsets of hippocampal neurons activated during learning, which enabled reliable identification. They then used 3D electron microscopy and artificial intelligence algorithms to produce nanoscale reconstructions of the excitatory neural networks involved in learning.
This study provides a comprehensive view of the structural hallmarks of memory formation in one brain region. It also raises new questions for further exploration. Future studies will be crucial in determining whether similar mechanisms operate across different time points and neural circuits. In addition, further investigation into the molecular composition of multi-synaptic boutons is needed to determine their precise role in memory and other cognitive processes.
The research was supported by funding from the National Institute of Mental Health, the National Institute of Neurological Disorders and Stroke, and NIH's Brain Research Through Advancing Innovative Neurotechnologies® Initiative, or The BRAIN Initiative®.
Who
Jamie Driscoll, National Institute of Mental Health and Dr. Eunyoung Kim, National Institute of Mental Health
Study
Uytiepo, M., Zhu, Y., Bushong, E., Chou, K., Polli, F. S., Zhao, E., Kim, K.-Y., Luu, D., Chang, L., Yang, D., Ma, T. C., Kim, M., Zhang, Y., Walton, G., Quach, T., Haber, M., Patapoutian, L., Shahbazi, A., Zhang, Y., … Maximov, A. (2025). Synaptic architecture of a memory engram in the mouse hippocampus. Science. http://www.science.org/doi/10.1126/science.ado8316
Brain Research Through Advancing Innovative Neurotechnologies® and The BRAIN Initiative® are registered trademarks of HHS.
