Summary: Automated robotic technology allows researchers to identify new pathways activated when the brain rewires circuits in response to experience.
Source: Carnegie Mellon University
We’ve all heard the saying that individuals learn at their own pace. Researchers at Carnegie Mellon University have developed an automated, robotic training device that allows mice to learn at their leisure. The technology stands to further neuroscience research by allowing researchers to train animals under more natural conditions and identify mechanisms of circuit rewiring that occur during learning.
A research team led by Carnegie Mellon neuroscientist Alison Barth has used the automated technology to identify new, previously unidentified pathways activated when the brain rewires its circuits in response to experience. Their findings are published online in Neuron.
Barth’s lab focuses on understanding the process by which cortical circuits receive sensory information and adapt to it in order to learn. Understanding the algorithm that underlies the changes in the brain’s learning circuitry will have important implications for creating engineered systems that use deep learning and artificial intelligence.
“Neural circuits in the cerebral cortex have had 3.5 billion years to evolve to become perfectly adapted to learning things,” said Barth, a professor of biological sciences and member of the Carnegie Mellon Neuroscience Institute. “There is valuable information about what happens in the brain that can be used to inform computations that need to change based on experience.”
To better study how the brain changes during sensory learning, the researchers constructed an army of automated robotic devices, in an effort that was spearheaded by Sarah Bernhard, an undergraduate student in Carnegie Mellon’s Department of Biological Sciences. These devices allowed mice to voluntarily approach a water port in their home cage where they would receive a gentle puff of air to their whiskers followed by a drop of water. If they approached the port and didn’t feel a puff of air, they wouldn’t get a drop of water. Eventually, they learned that a puff of air meant water and they would start to drink when they felt it.
“It was almost like we gave the mice homework. Some took 50 tries to learn, others took 400. Some learned early in the evening, others learned late at night. But they all learned and learned quickly,” said Barth. “One thing that is critical to learning is that you have to be ready to learn. This device let mice learn when they wanted and at their own pace.”
They found that when they used the device, the mice learned quickly and independently, with no intervention from the researchers. As a result, they could capture a larger data set that more accurately reflects the individual diversity in learning.
In the Neuron study, Barth and colleagues used the robotic device to determine what sensory learning pathways were conserved across the population, regardless of how long learning took. They found some surprising results.
The pathways that changed the most in response to the sensory stimulus, indicating learning, were not the ones they expected. It was commonly thought that in sensory learning information came from the skin, traveling rapidly to the neocortex through the thalamus. However, the research team found that this pathway remained relatively unchanged during sensory learning. Instead, they were surprised to find that the cortical synapses, responding to a high-order and more integrative part of the thalamus, were much more plastic.
“Our results suggest that the brain maintains the pathway that represents the fast sensory input, things that you want to know for certain in any given situation. The pathway that is responsible for processing more context-rich information is the one that is flexible,” Barth said.
“The brain keeps the original file but edits a copy of it.”
The results provide insight into the algorithm that the neocortex uses to rewire itself during learning. Barth plans to use this training paradigm to understand how and when different types of tasks and rewards can change the brain.
Nicholas Audette was the lead author on the study, and Ajit Ray and Luke Stewart of Carnegie Mellon’s Department of Biological Sciences also contributed. Audette and Barth are also members of the joint Carnegie Mellon and University of Pittsburgh Center for the Neural Basis of Cognition.
Funding: The research was funded by the Carnegie Mellon University Hillman Presidential Fellowship, the IISC-CMU BrainHub Postdoctoral Fellowship and the National Institutes of Health (NS088958).
Carnegie Mellon University
Jocelyn Duffy – Carnegie Mellon University
The image is in the public domain.
Original Research: Closed access
“Rapid Plasticity of Higher-Order Thalamocortical Inputs during Sensory Learning”. Nicholas J. Audette, Sarah M. Bernhard, Ajit Ray, Luke T. Stewart, Alison L. Barth.
Rapid Plasticity of Higher-Order Thalamocortical Inputs during Sensory Learning
• Mice learn a multi-whisker sensory association during automated home-cage training
• Training, but not sensory stimulation alone, causes rapid synaptic plasticity in S1
• Synaptic plasticity observed only in higher-order thalamocortical pathways
• POm thalamic inputs are strengthened sequentially, first on L5 and then on L2 Pyr
Neocortical circuits are sensitive to experience, showing both anatomical and electrophysiological changes in response to altered sensory input. We examined input- and cell-type-specific changes in thalamo- and intracortical pathways during learning using an automated, home-cage sensory association training (SAT) paradigm coupling multi-whisker stimulation to a water reward. We found that the posterior medial nucleus (POm) but not the ventral posterior medial (VPM) nucleus of the thalamus drives increased cortical activity after 24 h of SAT, when behavioral evidence of learning first emerges. Synaptic strengthening within the POm thalamocortical pathway was first observed at thalamic inputs to L5 and was not generated by sensory stimulation alone. Synaptic changes in L2 were delayed relative to L5, requiring 48 h of SAT to drive synaptic plasticity at thalamic and intracortical inputs onto L2 Pyr neurons. These data identify the POm thalamocortical circuit as a site of rapid synaptic plasticity during learning and suggest a temporal sequence to learning-evoked synaptic changes in the sensory cortex.