Evidence map›Paper›PMID 40638616›Full record

ArticleThe Journal of physiology2025

Out of the single-neuron straitjacket: Neurons within assemblies change selectivity and their reconfiguration underlies dynamic coding.

Fabrizio Londei, Francesco Ceccarelli, Giulia Arena, Lorenzo Ferrucci, Eleonora Russo, Emiliano Brunamonti, Aldo Genovesio

Abstract read
In one paragraph

Article in The Journal of physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
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  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Fabrizio LondeiDepartment of Physiology and Pharmacology, Sapienza University of Rome, Rome, Italy.ORCID 0000-0003-3088-8218
Francesco CeccarelliDepartment of Physiology and Pharmacology, Sapienza University of Rome, Rome, Italy.ORCID 0000-0001-7319-8204
Giulia ArenaDepartment of Physiology and Pharmacology, Sapienza University of Rome, Rome, Italy.
Lorenzo FerrucciDepartment of Physiology and Pharmacology, Sapienza University of Rome, Rome, Italy.ORCID 0000-0003-4967-2951
Eleonora RussoThe BioRobotics Institute, Department of Excellence in Robotics and AI, Scuola Superiore Sant'Anna, Pisa, Italy.ORCID 0000-0002-6215-6305
Emiliano BrunamontiDepartment of Physiology and Pharmacology, Sapienza University of Rome, Rome, Italy.ORCID 0000-0002-5119-6950
Aldo GenovesioInstitute of Biochemistry and Cell Biology (IBBC), National Research Council of Italy (CNR), Monterotondo Scalo, Roma, Italy.ORCID 0000-0003-2521-143X

Funding

Ministry of University and Research (MUR), National Recovery and Resilience Plan (NRRP), project MNESYS PE0000006Ministry of University and Research, project PRIN 2017 2017KZNZLN_004Ministry of University and Research, project PRIN 2022 B53D23014270006
6 · The paper itself

Abstract

We investigated cell assemblies in the frontal cortex of macaques during two discrimination tasks. Focusing on the period of goal-action transformation, we extracted spikes fired during assembly activation from the full neural activity and showed that the contribution of a neuron to assembly coding, when it co-ordinates with other assembly neurons, differs from its coding in isolation. Neurons, with their flexible participation to multiple assemblies, contributed to the encoding of new information not encoded by the neurons alone. Even non-discriminative neurons acquired selectivity as part of the collective activity of the assemblies. Thus, neurons in their assemblies process distinct information for various purposes as a chess simul master, playing on multiple chessboards. The reconfiguration of the participation of the neurons into different assemblies in the goal-action transformation process translated into a dynamic form of coding, whereas minimal reconfiguration was associated with the static goal coding of the memory period. KEY POINTS: Traditionally, the coding properties of a neuron are studied using all its activity (full-spikes), irrespective of its co-ordination with different groups of neurons. With an assembly centered approach, we can determine the neuron's coding properties not in absolute terms, but relative to the assembly of neurons with which it co-ordinates. When neurons are studied in different assemblies-focusing only on the spikes fired during assembly coordination (assembly-spikes)-they can contribute to the coding of different variables. The coding flexibility of the same neuron in multiple assemblies increases the amount of information it can contribute to encoding compared to isolated neurons. Dynamic coding, as opposed to static coding, as observed during the goal-action transformation process, can be explained by an increase in the reconfiguration of active assemblies, with neurons contributing to the coding of different variables in different epochs, depending on which assembly is active.

Indexed as

Frontal LobeNeuronsAction PotentialsAnimalsMacaca mulattaMaleassemblydynamicmonkeyprefrontalreconfigurationstatic

Identifiers

PMID40638616
PMCPMC12320208

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.