Summary: Researchers have identified a signaling pathway in the hippocampus that plays a critical role in creating novel memories about new environments.
Source: IST Austria
Imagine going to a café you have never been to. You will remember this new environment, but when you visit it again and again fewer new memories about the environment will be formed, only the things that changed will be really memorable. How this long-term memory are regulated is still not fully understood. Ryuichi Shigemoto from the Institute of Science and Technology Austria (IST Austria) in cooperation with researchers from Aarhus University and the National Institute for Physiological Sciences in Japan now have uncovered a new keystone in the formation of memories.
In their study published in Current Biology, they investigated a signaling path in the hippocampus area of the brain and showed how it controls making new memories about experiencing new environments.
The hippocampus is a central area in the brain that plays an important role in transferring information from the short-term memory to the long-term memory. Of the many interlocking parts of the hippocampus, the researchers focused on the connection between the so-called mossy cells that receive novelty signals of sensory input about the environment and the so-called granule cells to which this information is relayed. In diseases like Alzheimer’s this part of the brain is one of the first ones affected.
Watching Neurons
The scientists used four different approaches for this study in order to rigorously investigate these new findings. First, they put the hippocampus under the microscope and studied the structure of how the mossy cells are connected to the granule cells showing their many complex connections.
Second, they used the technique of calcium imaging that allows live monitoring of neuron activity as these genetically modified cells light up when activated. When exposing the animals a new environment for several days, the activity of the mossy cells sending signals to the granule cells first was high and then became less and less. When they then put the mice into another new environment, the activity sprung up again, therefore showing that these neurons are specifically relevant to process new environmental input.
Third, the researchers followed traces in the neuron left by the signals. Neural activity in these cells triggers the expression of a certain gene, meaning the production of the corresponding protein that is encoded in it. The more activity there was, the more of this protein they can find afterwards. In the granule cells they found production of this protein, which correlated with activity of the mossy cells.
Dreading New Places
And lastly, the scientists used behavioral studies to see the effects of this pathway in the hippocampus on memory formation. This is especially important, because the connection between memory formation and behavior can tell them a lot about the brain’s functions. They combined a negative sensory stimulus, a small electric shock, with putting the animals in a new environment. The mice then quickly learned to associate the new environment with unpleasant feelings and their negative reaction of freezing on the spot was measured.
When the researches used drugs to inhibit the activity of the mossy cells–the ones receiving the signals about the new environment–and then did the negative conditioning, the mice did not remember the connection between the new environment and the unpleasant feeling. Additionally, when the animals were first accustomed to the new environment and then conditioned, there was also no activation of the mossy cells, and therefore no association between the environment and the shocks.
On the other hand, if the mossy cells were artificially activated, this association could be formed even after the animals were already used to the new environment. This clearly shows how the mossy cells in the hippocampus react to novel input and trigger the formation of new long-term memories in mice.
Next Steps in Understanding
Whether the exact same processes happen in the human brain is still an open question, but these new findings are an important first step in understanding this part of our most complex organ. Ryuichi Shigemoto and his collaborators are conducting fundamental research that may one day help to address degenerative brain diseases that affect memory formation, but this is still a while away.
He cautiously states: “This research field is very competitive and new findings arise quickly. There are many disputed mechanisms on memory formation, but our findings corroborate an existing hypothesis and are very robust, thus opening up a new field of neuroscience research and furthering our understanding of the brain.”
Animal welfare
Understanding how the brain stores and processes information is only possible by studying the brains of animals while they carry out specific behaviors. No other methods, such as in vitro or in silico models, can serve as alternatives. The animals were raised, kept and treated according to the strict regulations of Austrian law.
About this memory research news
Source: IST Austria
Contact: Patrick Müller – IST Austria
Image: The image is credited to Ryuichi Shigemoto.
Original Research: Open access.
“Ventro-dorsal Hippocampal Pathway Gates Novelty-Induced Contextual Memory Formation” by Ryuichi Shigemoto et al. Current Biology
Abstract
Ventro-dorsal Hippocampal Pathway Gates Novelty-Induced Contextual Memory Formation
Highlights
- •Mossy cells in ventral hilus directly excite granule cells in dorsal hippocampus
- •Activity of ventral mossy cells positively correlates with environmental novelty
- •Inhibiting ventral mossy cells disrupts novelty-induced contextual fear memory
- •Exciting ventral mossy cells enhances contextual memory in a familiar environment
Summary
Novelty facilitates memory formation and is detected by both the dorsal and ventral hippocampus. Although dentate granule cells (GCs) in the dorsal hippocampus are known to mediate the formation of novelty-induced contextual memories, the required pathways and mechanisms remain unclear. Here we demonstrate that a powerful excitatory pathway from mossy cells (MCs) in the ventral hippocampus to dorsal GCs is necessary and sufficient for driving dorsal GC activation in novel environment exploration. In vivo Ca2+ imaging in freely moving mice indicated that this pathway relays environmental novelty. Furthermore, manipulation of ventral MC activity bidirectionally regulates novelty-induced contextual memory acquisition. Our results show that ventral MC activity gates contextual memory formation through an intra-hippocampal interaction activated by environmental novelty.
