» Articles » PMID: 37910428

Mega-scale Movie-fields in the Mouse Visuo-hippocampal Network

Overview
Journal Elife
Specialty Biology
Date 2023 Nov 1
PMID 37910428
Authors
Affiliations
Soon will be listed here.
Abstract

Natural visual experience involves a continuous series of related images while the subject is immobile. How does the cortico-hippocampal circuit process a visual episode? The hippocampus is crucial for episodic memory, but most rodent single unit studies require spatial exploration or active engagement. Hence, we investigated neural responses to a silent movie (Allen Brain Observatory) in head-fixed mice without any task or locomotion demands, or rewards. Surprisingly, a third (33%, 3379/10263) of hippocampal -dentate gyrus, CA3, CA1 and subiculum- neurons showed movie-selectivity, with elevated firing in specific movie sub-segments, termed movie-fields, similar to the vast majority of thalamo-cortical (LGN, V1, AM-PM) neurons (97%, 6554/6785). Movie-tuning remained intact in immobile or spontaneously running mice. Visual neurons had >5 movie-fields per cell, but only ~2 in hippocampus. The movie-field durations in all brain regions spanned an unprecedented 1000-fold range: from 0.02s to 20s, termed mega-scale coding. Yet, the total duration of all the movie-fields of a cell was comparable across neurons and brain regions. The hippocampal responses thus showed greater continuous-sequence encoding than visual areas, as evidenced by fewer and broader movie-fields than in visual areas. Consistently, repeated presentation of the movie images in a fixed, but scrambled sequence virtually abolished hippocampal but not visual-cortical selectivity. The preference for continuous, compared to scrambled sequence was eight-fold greater in hippocampal than visual areas, further supporting episodic-sequence encoding. Movies could thus provide a unified way to probe neural mechanisms of episodic information processing and memory, even in immobile subjects, across brain regions, and species.

Citing Articles

Hippocampal neuronal activity is aligned with action plans.

Zutshi I, Apostolelli A, Yang W, Zheng Z, Dohi T, Balzani E Nature. 2025; 639(8053):153-161.

PMID: 39779866 DOI: 10.1038/s41586-024-08397-7.


Recurrent cortical networks encode natural sensory statistics via sequence filtering.

Deveau C, Zhou Z, LaFosse P, Deng Y, Mirbagheri S, Steinmetz N bioRxiv. 2024; .

PMID: 38903066 PMC: 11188075. DOI: 10.1101/2024.02.24.581890.


Sharing neurophysiology data from the Allen Brain Observatory.

de Vries S, Siegle J, Koch C Elife. 2023; 12.

PMID: 37432073 PMC: 10335829. DOI: 10.7554/eLife.85550.

References
1.
Sharp P, Green C . Spatial correlates of firing patterns of single cells in the subiculum of the freely moving rat. J Neurosci. 1994; 14(4):2339-56. PMC: 6577112. View

2.
Jacobs J, Kahana M, Ekstrom A, Mollison M, Fried I . A sense of direction in human entorhinal cortex. Proc Natl Acad Sci U S A. 2010; 107(14):6487-92. PMC: 2851993. DOI: 10.1073/pnas.0911213107. View

3.
Saleem A, Diamanti E, Fournier J, Harris K, Carandini M . Coherent encoding of subjective spatial position in visual cortex and hippocampus. Nature. 2018; 562(7725):124-127. PMC: 6309439. DOI: 10.1038/s41586-018-0516-1. View

4.
Kjelstrup K, Solstad T, Brun V, Hafting T, Leutgeb S, Witter M . Finite scale of spatial representation in the hippocampus. Science. 2008; 321(5885):140-3. DOI: 10.1126/science.1157086. View

5.
Froudarakis E, Berens P, Ecker A, Cotton R, Sinz F, Yatsenko D . Population code in mouse V1 facilitates readout of natural scenes through increased sparseness. Nat Neurosci. 2014; 17(6):851-7. PMC: 4106281. DOI: 10.1038/nn.3707. View