Intrinsic neural excitability biases allocation and overlap of memory engrams

Delamare G, Feitosa Tomé D, Clopath C. 2024. Intrinsic neural excitability biases allocation and overlap of memory engrams. Journal of Neuroscience. 44(21), e0846232024.

Download
OA 2024_JourNeuroscience_Delamare.pdf 920.35 KB [Published Version]

Journal Article | Published | English

Scopus indexed
Author
Delamare, Geoffroy; Feitosa Tomé, DouglasISTA; Clopath, Claudia
Department
Abstract
Memories are thought to be stored in neural ensembles known as engrams that are specifically reactivated during memory recall. Recent studies have found that memory engrams of two events that happened close in time tend to overlap in the hippocampus and the amygdala, and these overlaps have been shown to support memory linking. It has been hypothesized that engram overlaps arise from the mechanisms that regulate memory allocation itself, involving neural excitability, but the exact process remains unclear. Indeed, most theoretical studies focus on synaptic plasticity and little is known about the role of intrinsic plasticity, which could be mediated by neural excitability and serve as a complementary mechanism for forming memory engrams. Here, we developed a rate-based recurrent neural network that includes both synaptic plasticity and neural excitability. We obtained structural and functional overlap of memory engrams for contexts that are presented close in time, consistent with experimental and computational studies. We then investigated the role of excitability in memory allocation at the network level and unveiled competitive mechanisms driven by inhibition. This work suggests mechanisms underlying the role of intrinsic excitability in memory allocation and linking, and yields predictions regarding the formation and the overlap of memory engrams.
Publishing Year
Date Published
2024-05-22
Journal Title
Journal of Neuroscience
Acknowledgement
We thank Sadra Sadeh and Inês Completo Guerreiro for helpful comments on the manuscript, Yosif Zaki and Denise J. Cai for useful feedback and members of the Clopath lab for discussion and support. This work was supported by Biotechnology and Biological Sciences Research Council (BB/N013956/1 awarded to C.C.), Wellcome Trust (200790/Z/16/Z awarded to C.C.), the Simons Foundation (564408 awarded to C.C.), and Engineering and Physical Sciences Research Council (EP/R035806/1 awarded to C.C.).
Volume
44
Issue
21
Article Number
e0846232024
ISSN
eISSN
IST-REx-ID

Cite this

Delamare G, Feitosa Tomé D, Clopath C. Intrinsic neural excitability biases allocation and overlap of memory engrams. Journal of Neuroscience. 2024;44(21). doi:10.1523/JNEUROSCI.0846-23.2024
Delamare, G., Feitosa Tomé, D., & Clopath, C. (2024). Intrinsic neural excitability biases allocation and overlap of memory engrams. Journal of Neuroscience. Society of Neuroscience. https://doi.org/10.1523/JNEUROSCI.0846-23.2024
Delamare, Geoffroy, Douglas Feitosa Tomé, and Claudia Clopath. “Intrinsic Neural Excitability Biases Allocation and Overlap of Memory Engrams.” Journal of Neuroscience. Society of Neuroscience, 2024. https://doi.org/10.1523/JNEUROSCI.0846-23.2024.
G. Delamare, D. Feitosa Tomé, and C. Clopath, “Intrinsic neural excitability biases allocation and overlap of memory engrams,” Journal of Neuroscience, vol. 44, no. 21. Society of Neuroscience, 2024.
Delamare G, Feitosa Tomé D, Clopath C. 2024. Intrinsic neural excitability biases allocation and overlap of memory engrams. Journal of Neuroscience. 44(21), e0846232024.
Delamare, Geoffroy, et al. “Intrinsic Neural Excitability Biases Allocation and Overlap of Memory Engrams.” Journal of Neuroscience, vol. 44, no. 21, e0846232024, Society of Neuroscience, 2024, doi:10.1523/JNEUROSCI.0846-23.2024.
All files available under the following license(s):
Creative Commons Attribution 4.0 International Public License (CC-BY 4.0):
Main File(s)
Access Level
OA Open Access
Date Uploaded
2024-06-03
MD5 Checksum
4e19159800db605b802c721e4d4b1ffe


Export

Marked Publications

Open Data ISTA Research Explorer

Sources

PMID: 38561228
PubMed | Europe PMC

Search this title in

Google Scholar