Competitive processes shape multi-synapse plasticity along dendritic segments

Neurons receive thousands of inputs onto their dendritic arbour, where individual synapses undergo activity-dependent plasticity. Long-lasting changes in postsynaptic strengths correlate with changes in spine head volume. The magnitude and direction of such structural plasticity - potentiation (sLTP) and depression (sLTD) - depend upon the number and spatial distribution of stimulated synapses. However, how neurons allocate resources to implement synaptic strength changes across space and time amongst neighbouring synapses remains unclear. Here we combined experimental and modelling approaches to explore the elementary processes underlying multi-spine plasticity. We used glutamate uncaging to induce sLTP at varying number of synapses sharing the same dendritic branch, and we built a model incorporating a dual role Ca<sup>2+</sup>-dependent component that induces spine growth or shrinkage. Our results suggest that competition among spines for molecular resources is a key driver of multi-spine plasticity and that spatial distance between simultaneously stimulated spines impacts the resulting spine dynamics.

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Publication Details

Journal
Nature Communications
Published
2024-08-31
DOI
https://doi.org/10.1038/s41467-024-51919-0
Citations
15
Primary Topic
Neuroscience and Neuropharmacology Research
Type
article
Field-Weighted Citation Impact
4.02

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article

Competitive processes shape multi-synapse plasticity along dendritic segments

Tatjana Tchumatchenko, Maximilian F. Eggl, Yukiko Goda, Thomas E. Chater
15 citations
Nature Communications
Neuroscience and Neuropharmacology Research
4.02
article

Competitive processes shape multi-synapse plasticity along dendritic segments

Tatjana Tchumatchenko, Maximilian F. Eggl, Yukiko Goda, Thomas E. Chater
article en
15 citations

Abstract

Neurons receive thousands of inputs onto their dendritic arbour, where individual synapses undergo activity-dependent plasticity. Long-lasting changes in postsynaptic strengths correlate with changes in spine head volume. The magnitude and direction of such structural plasticity - potentiation (sLTP) and depression (sLTD) - depend upon the number and spatial distribution of stimulated synapses. However, how neurons allocate resources to implement synaptic strength changes across space and time amongst neighbouring synapses remains unclear. Here we combined experimental and modelling approaches to explore the elementary processes underlying multi-spine plasticity. We used glutamate uncaging to induce sLTP at varying number of synapses sharing the same dendritic branch, and we built a model incorporating a dual role Ca<sup>2+</sup>-dependent component that induces spine growth or shrinkage. Our results suggest that competition among spines for molecular resources is a key driver of multi-spine plasticity and that spatial distance between simultaneously stimulated spines impacts the resulting spine dynamics.

Nature CommunicationsVol. 15(1)
University of Bonn (DE), Okinawa Institute of Science and Technology Graduate University (JP), Keio University (JP), University Hospital Bonn (DE), RIKEN Center for Brain Science (JP), Instituto de Neurociencias (ES)
Joachim Herz Stiftung, European Commission, Okinawa Institute of Science and Technology Graduate University, Rheinische Friedrich-Wilhelms-Universität Bonn, Japan Society for the Promotion of Science, RIKEN
Openalex Percentile: Top 5%
Neuroscience and Neuropharmacology Research
4.02
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