Evidence map›Paper›PMID 36865334›Full record

ArticlebioRxiv : the preprint server for biology2023

Single neurons in the human medial temporal lobe flexibly shift representations across spatial and memory tasks.

Thomas Donoghue, Runnan Cao, Claire Z Han, Cameron M Holman, Nicholas J Brandmeir, Shuo Wang, Joshua Jacobs

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Thomas DonoghueDepartment of Biomedical Engineering, Columbia University.
Runnan CaoLane Department of Computer Science and Electrical Engineering, West Virginia University.
Claire Z HanDepartment of Biomedical Engineering, Columbia University.
Cameron M HolmanDepartment of Biomedical Engineering, Columbia University.
Nicholas J BrandmeirDepartment of Neurosurgery, West Virginia University.
Shuo WangDepartment of Radiology, Washington University in St. Louis.
Joshua JacobsDepartment of Biomedical Engineering, Columbia University.

Funding

The Role of Place and Grid Cells in Human Spatial Navigation and MemoryR01MH104606 · NIMH · UNIVERSITY OF CHICAGO · PI Joshua Jacobs · 2015 to 2026
$6.5M
Model-Based Investigation of Aberrant Neural Face Representation in AutismR01MH129426 · NIMH · WASHINGTON UNIVERSITY · PI Shuo Wang · 2022 to 2026
$1.9M
NIMH NIH HHS R01 MH104606NIMH NIH HHS R01 MH129426
6 · The paper itself

Abstract

Investigations into how individual neurons encode behavioral variables of interest have revealed specific representations in single neurons, such as place and object cells, as well as a wide range of cells with conjunctive encodings or mixed selectivity. However, as most experiments examine neural activity within individual tasks, it is currently unclear if and how neural representations change across different task contexts. Within this discussion, the medial temporal lobe is particularly salient, as it is known to be important for multiple behaviors including spatial navigation and memory, however the relationship between these functions is currently unclear. Here, to investigate how representations in single neurons vary across different task contexts in the MTL, we collected and analyzed single-neuron activity from human participants as they completed a paired-task session consisting of a passive-viewing visual working memory and a spatial navigation and memory task. Five patients contributed 22 paired-task sessions, which were spike sorted together to allow for the same putative single neurons to be compared between the different tasks. Within each task, we replicated concept-related activations in the working memory task, as well as target-location and serial-position responsive cells in the navigation task. When comparing neuronal activity between tasks, we first established that a significant number of neurons maintained the same kind of representation, responding to stimuli presentations across tasks. Further, we found cells that changed the nature of their representation across tasks, including a significant number of cells that were stimulus responsive in the working memory task that responded to serial position in the spatial task. Overall, our results support a flexible encoding of multiple, distinct aspects of different tasks by single neurons in the human MTL, whereby some individual neurons change the nature of their feature coding between task contexts.

Identifiers

PMID36865334
PMCPMC9980106

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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.