Summary: A new study reports researchers have successfully generated an artificial memory by injecting a sea snail with the RNA from another. Researchers say this approach could lead to new treatments to restore memory and alter traumatic memories in humans.
UCLA biologists report they have transferred a memory from one marine snail to another, creating an artificial memory, by injecting RNA from one to another. This research could lead to new ways to lessen the trauma of painful memories with RNA and to restore lost memories.
“I think in the not-too-distant future, we could potentially use RNA to ameliorate the effects of Alzheimer’s disease or post-traumatic stress disorder,” said David Glanzman, senior author of the study and a UCLA professor of integrative biology and physiology and of neurobiology. The team’s research is published May 14 in eNeuro.
RNA, or ribonucleic acid, has been widely known as a cellular messenger that makes proteins and carries out DNA’s instructions to other parts of the cell. It is now understood to have other important functions besides protein coding, including regulation of a variety of cellular processes involved in development and disease.
The researchers gave mild electric shocks to the tails of a species of marine snail called Aplysia. The snails received five tail shocks, one every 20 minutes, and then five more 24 hours later. The shocks enhance the snail’s defensive withdrawal reflex, a response it displays for protection from potential harm. When the researchers subsequently tapped the snails, they found those that had been given the shocks displayed a defensive contraction that lasted an average of 50 seconds, a simple type of learning known as “sensitization.” Those that had not been given the shocks contracted for only about one second.
The life scientists extracted RNA from the nervous systems of marine snails that received the tail shocks the day after the second series of shocks, and also from marine snails that did not receive any shocks. Then the RNA from the first (sensitized) group was injected into seven marine snails that had not received any shocks, and the RNA from the second group was injected into a control group of seven other snails that also had not received any shocks.
Remarkably, the scientists found that the seven that received the RNA from snails that were given the shocks behaved as if they themselves had received the tail shocks: They displayed a defensive contraction that lasted an average of about 40 seconds.
“It’s as though we transferred the memory,” said Glanzman, who is also a member of UCLA’s Brain Research Institute.
As expected, the control group of snails did not display the lengthy contraction.
Next, the researchers added RNA to Petri dishes containing neurons extracted from different snails that did not receive shocks. Some dishes had RNA from marine snails that had been given electric tail shocks, and some dishes contained RNA from snails that had not been given shocks. Some of the dishes contained sensory neurons, and others contained motor neurons, which in the snail are responsible for the reflex.
When a marine snail is given electric tail shocks, its sensory neurons become more excitable. Interestingly, the researchers discovered, adding RNA from the snails that had been given shocks also produced increased excitability in sensory neurons in a Petri dish; it did not do so in motor neurons. Adding RNA from a marine snail that was not given the tail shocks did not produce this increased excitability in sensory neurons.
In the field of neuroscience, it has long been thought that memories are stored in synapses. (Each neuron has several thousand synapses.) Glanzman holds a different view, believing that memories are stored in the nucleus of neurons.
“If memories were stored at synapses, there is no way our experiment would have worked,” said Glanzman, who added that the marine snail is an excellent model for studying the brain and memory.
Scientists know more about the cell biology of this simple form of learning in this animal than any other form of learning in any other organism, Glanzman said. The cellular and molecular processes seem to be very similar between the marine snail and humans, even though the snail has about 20,000 neurons in its central nervous system and humans are thought to have about 100 billion.
In the future, Glanzman said, it is possible that RNA can be used to awaken and restore memories that have gone dormant in the early stages of Alzheimer’s disease. He and his colleagues published research in the journal eLife in 2014 indicating that lost memories can be restored.
There are many kinds of RNA, and in future research, Glanzman wants to identify the types of RNA that can be used to transfer memories.
Co-authors are Alexis Bédécarrats, a UCLA postdoctoral scholar who worked in Glanzman’s laboratory; and Shanping Chen, Kaycey Pearce and Diancai Cai, research associates in Glanzman’s laboratory.
Funding: The research was funded by the National Institute of Neurological Disorders and Stroke, the National Institute of Mental Health and the National Science Foundation.
Source: Stuart Wolpert – UCLA
Publisher: Organized by NeuroscienceNews.com.
Image Source: NeuroscienceNews.com image is in the public domain.
Original Research: Abstract for “RNA from Trained Aplysia Can Induce an Epigenetic Engram for Long-Term Sensitization in Untrained Aplysia” by Alexis Bédécarrats, Shanping Chen, Kaycey Pearce, Diancai Cai and David L. Glanzman in eNeuro. Published May 14 2018.
[cbtabs][cbtab title=”MLA”]UCLA “Researchers ‘Transfer’ a Memory.” NeuroscienceNews. NeuroscienceNews, 14 May 2018.
<https://neurosciencenews.com/memory-transfer-9042/>.[/cbtab][cbtab title=”APA”]UCLA (2018, May 14). Researchers ‘Transfer’ a Memory. NeuroscienceNews. Retrieved May 14, 2018 from https://neurosciencenews.com/memory-transfer-9042/[/cbtab][cbtab title=”Chicago”]UCLA “Researchers ‘Transfer’ a Memory.” https://neurosciencenews.com/memory-transfer-9042/ (accessed May 14, 2018).[/cbtab][/cbtabs]
RNA from Trained Aplysia Can Induce an Epigenetic Engram for Long-Term Sensitization in Untrained Aplysia
The precise nature of the engram, the physical substrate of memory, remains uncertain. Here, it is reported that RNA extracted from the central nervous system of Aplysia given long-term sensitization training induced sensitization when injected into untrained animals; furthermore, the RNA-induced sensitization, like training-induced sensitization, required DNA methylation. In cellular experiments, treatment with RNA extracted from trained animals was found to increase excitability in sensory neurons, but not in motor neurons, dissociated from naïve animals. Thus, the behavioral, and a subset of the cellular, modifications characteristic of a form of nonassociative long-term memory in Aplysia can be transferred by RNA. These results indicate that RNA is sufficient to generate an engram for long-term sensitization in Aplysia and are consistent with the hypothesis that RNA-induced epigenetic changes underlie memory storage in Aplysia.
Significance Statement It is generally accepted that long-term memory (LTM) is encoded as alterations in synaptic strength. An alternative model, however, proposes that LTM is encoded by epigenetic changes. Non-coding RNAs can mediate epigenetic modifications. Therefore, RNA from a trained animal might be capable of producing learning-like behavioral change in an untrained animal. Here, it is demonstrated that the memory for long-term sensitization in the marine mollusk Aplysia can be successfully transferred by injecting RNA from sensitized into naïve animals. Moreover, a specific cellular alteration that underlies sensitization in Aplysia, sensory neuron hyperexcitability, can be reproduced by exposing sensory neurons in vitro to RNA from trained animals. The results provide support for a nonsynaptic, epigenetic model of memory storage in Aplysia.