Nonlinear manifolds underlie neural population activity during behaviour.


Journal

bioRxiv : the preprint server for biology
Titre abrégé: bioRxiv
Pays: United States
ID NLM: 101680187

Informations de publication

Date de publication:
21 Jul 2023
Historique:
pubmed: 28 7 2023
medline: 28 7 2023
entrez: 28 7 2023
Statut: epublish

Résumé

There is rich variety in the activity of single neurons recorded during behaviour. Yet, these diverse single neuron responses can be well described by relatively few patterns of neural co-modulation. The study of such low-dimensional structure of neural population activity has provided important insights into how the brain generates behaviour. Virtually all of these studies have used linear dimensionality reduction techniques to estimate these population-wide co-modulation patterns, constraining them to a flat "neural manifold". Here, we hypothesised that since neurons have nonlinear responses and make thousands of distributed and recurrent connections that likely amplify such nonlinearities, neural manifolds should be intrinsically nonlinear. Combining neural population recordings from monkey motor cortex, mouse motor cortex, mouse striatum, and human motor cortex, we show that: 1) neural manifolds are intrinsically nonlinear; 2) the degree of their nonlinearity varies across architecturally distinct brain regions; and 3) manifold nonlinearity becomes more evident during complex tasks that require more varied activity patterns. Simulations using recurrent neural network models confirmed the proposed relationship between circuit connectivity and manifold nonlinearity, including the differences across architecturally distinct regions. Thus, neural manifolds underlying the generation of behaviour are inherently nonlinear, and properly accounting for such nonlinearities will be critical as neuroscientists move towards studying numerous brain regions involved in increasingly complex and naturalistic behaviours.

Identifiants

pubmed: 37503015
doi: 10.1101/2023.07.18.549575
pmc: PMC10370078
pii:
doi:

Banques de données

Dryad
['10.5061/dryad.xd2547dkt']

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS053603
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS074044
Pays : United States

Auteurs

Cátia Fortunato (C)

Department of Bioengineering, Imperial College London, London UK.

Jorge Bennasar-Vázquez (J)

Department of Bioengineering, Imperial College London, London UK.

Junchol Park (J)

Janelia Research Campus, Howard Hughes Medical Institute, Ashburn VA, USA.

Joanna C Chang (JC)

Department of Bioengineering, Imperial College London, London UK.

Lee E Miller (LE)

Department of Neurosciences, Northwestern University, Chicago IL, USA.
Department of Biomedical Engineering, Northwestern University, Chicago IL, USA.
Department of Physical Medicine and Rehabilitation, Northwestern University, Chicago IL, USA, and Shirley Ryan Ability Lab, Chicago, IL, USA.

Joshua T Dudman (JT)

Janelia Research Campus, Howard Hughes Medical Institute, Ashburn VA, USA.

Matthew G Perich (MG)

Department of Neurosciences, Faculté de médecine, Université de Montréal, Montréal, Québec, Canada.
Québec Artificial Intelligence Institute (MILA), Montréal, Québec, Canada.

Juan A Gallego (JA)

Department of Bioengineering, Imperial College London, London UK.

Classifications MeSH