Evidence map›Paper›PMID 40956839›Full record

ArticlePLoS computational biology2025

Dynamical mean-field theory for a highly heterogeneous neural population with graded persistent activity of the entorhinal cortex.

Futa Tomita, Jun-Nosuke Teramae

Abstract read
In one paragraph

Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

2 authors.

Futa TomitaGraduate School of Informatics, Kyoto University, Kyoto, Japan.ORCID 0009-0005-1793-8489
Jun-Nosuke TeramaeGraduate School of Informatics, Kyoto University, Kyoto, Japan.

Funding

Japan Agency for Medical Research and Development (AMED)Japan Science and Technology Agency (JST)Japan Society for the Promotion of Science (JSPS)
6 · The paper itself

Abstract

The entorhinal cortex serves as a major gateway connecting the hippocampus and neocortex, playing a pivotal role in episodic memory formation. Neurons in the entorhinal cortex exhibit two notable features associated with temporal information processing: a population-level ability to encode long temporal signals and a single-cell characteristic known as graded-persistent activity, where some neurons maintain activity for extended periods even without external inputs. However, the relationship between these single-cell characteristics and population dynamics has remained unclear, largely due to the absence of a framework to describe the dynamics of neural populations with highly heterogeneous time scales. To address this gap, we extend the dynamical mean field theory, a powerful framework for analyzing large-scale population dynamics, to study the dynamics of heterogeneous neural populations. By proposing an analytically tractable model of graded-persistent activity, we demonstrate that the introduction of graded-persistent neurons shifts the chaos-order phase transition point and expands the network's dynamical region, a preferable region for temporal information computation. Furthermore, we validate our framework by applying it to a system with heterogeneous adaptation, demonstrating that such heterogeneity can reduce the dynamical regime, contrary to previous simplified approximations. These findings establish a theoretical foundation for understanding the functional advantages of diversity in biological systems and offer insights applicable to a wide range of heterogeneous networks beyond neural populations.

Indexed as

Entorhinal CortexModels, NeurologicalNeuronsAnimalsComputational BiologyComputer SimulationHumansNerve Net

Identifiers

PMID40956839
PMCPMC12456838

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.