» Articles » PMID: 39143207

Abstract Representations Emerge in Human Hippocampal Neurons During Inference

Overview
Journal Nature
Specialty Science
Date 2024 Aug 14
PMID 39143207
Authors
Affiliations
Soon will be listed here.
Abstract

Humans have the remarkable cognitive capacity to rapidly adapt to changing environments. Central to this capacity is the ability to form high-level, abstract representations that take advantage of regularities in the world to support generalization. However, little is known about how these representations are encoded in populations of neurons, how they emerge through learning and how they relate to behaviour. Here we characterized the representational geometry of populations of neurons (single units) recorded in the hippocampus, amygdala, medial frontal cortex and ventral temporal cortex of neurosurgical patients performing an inferential reasoning task. We found that only the neural representations formed in the hippocampus simultaneously encode several task variables in an abstract, or disentangled, format. This representational geometry is uniquely observed after patients learn to perform inference, and consists of disentangled directly observable and discovered latent task variables. Learning to perform inference by trial and error or through verbal instructions led to the formation of hippocampal representations with similar geometric properties. The observed relation between representational format and inference behaviour suggests that abstract and disentangled representational geometries are important for complex cognition.

Citing Articles

Adaptation shapes the representational geometry in mouse V1 to efficiently encode the environment.

Dipoppa M, Nogueira R, Bugeon S, Friedman Y, Reddy C, Harris K bioRxiv. 2025; .

PMID: 39896460 PMC: 11785004. DOI: 10.1101/2024.12.11.628035.


Linking neural population formatting to function.

Ruff D, Markman S, Kim J, Cohen M bioRxiv. 2025; .

PMID: 39803479 PMC: 11722384. DOI: 10.1101/2025.01.03.631242.


Domain-specific representation of social inference by neurons in the human amygdala and hippocampus.

Cao R, DuBois J, Mamelak A, Adolphs R, Wang S, Rutishauser U Sci Adv. 2024; 10(49):eado6166.

PMID: 39630898 PMC: 11616683. DOI: 10.1126/sciadv.ado6166.


Rarely categorical, always high-dimensional: how the neural code changes along the cortical hierarchy.

Posani L, Wang S, Muscinelli S, Muscinelli S, Paninski L, Fusi S bioRxiv. 2024; .

PMID: 39605683 PMC: 11601379. DOI: 10.1101/2024.11.15.623878.


Human single-neuron activity is modulated by intracranial theta burst stimulation of the basolateral amygdala.

Campbell J, Cowan R, Wahlstrom K, Hollearn M, Jensen D, Davis T bioRxiv. 2024; .

PMID: 39605345 PMC: 11601271. DOI: 10.1101/2024.11.11.622161.


References
1.
TOLMAN E . Cognitive maps in rats and men. Psychol Rev. 1948; 55(4):189-208. DOI: 10.1037/h0061626. View

2.
Chung S, Abbott L . Neural population geometry: An approach for understanding biological and artificial neural networks. Curr Opin Neurobiol. 2021; 70:137-144. PMC: 10695674. DOI: 10.1016/j.conb.2021.10.010. View

3.
Whittington J, McCaffary D, Bakermans J, Behrens T . How to build a cognitive map. Nat Neurosci. 2022; 25(10):1257-1272. DOI: 10.1038/s41593-022-01153-y. View

4.
Tenenbaum J, Kemp C, Griffiths T, Goodman N . How to grow a mind: statistics, structure, and abstraction. Science. 2011; 331(6022):1279-85. DOI: 10.1126/science.1192788. View

5.
Kemp C, Tenenbaum J . Structured statistical models of inductive reasoning. Psychol Rev. 2009; 116(1):20-58. DOI: 10.1037/a0014282. View