Diversity of visual inputs to Kenyon cells of the Drosophila mushroom body.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
07 Jul 2024
Historique:
received: 24 01 2024
accepted: 11 06 2024
medline: 8 7 2024
pubmed: 8 7 2024
entrez: 7 7 2024
Statut: epublish

Résumé

The arthropod mushroom body is well-studied as an expansion layer representing olfactory stimuli and linking them to contingent events. However, 8% of mushroom body Kenyon cells in Drosophila melanogaster receive predominantly visual input, and their function remains unclear. Here, we identify inputs to visual Kenyon cells using the FlyWire adult whole-brain connectome. Input repertoires are similar across hemispheres and connectomes with certain inputs highly overrepresented. Many visual neurons presynaptic to Kenyon cells have large receptive fields, while interneuron inputs receive spatially restricted signals that may be tuned to specific visual features. Individual visual Kenyon cells randomly sample sparse inputs from combinations of visual channels, including multiple optic lobe neuropils. These connectivity patterns suggest that visual coding in the mushroom body, like olfactory coding, is sparse, distributed, and combinatorial. However, the specific input repertoire to the smaller population of visual Kenyon cells suggests a constrained encoding of visual stimuli.

Identifiants

pubmed: 38972924
doi: 10.1038/s41467-024-49616-z
pii: 10.1038/s41467-024-49616-z
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5698

Informations de copyright

© 2024. The Author(s).

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Auteurs

Ishani Ganguly (I)

Department of Neuroscience, Columbia University, New York, NY, USA.
Center for Theoretical Neuroscience, Columbia University, New York, NY, USA.
Zuckerman Institute, Columbia University, New York, NY, USA.

Emily L Heckman (EL)

Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.

Ashok Litwin-Kumar (A)

Department of Neuroscience, Columbia University, New York, NY, USA.
Center for Theoretical Neuroscience, Columbia University, New York, NY, USA.
Zuckerman Institute, Columbia University, New York, NY, USA.

E Josephine Clowney (EJ)

Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, USA. jclowney@umich.edu.
Michigan Neuroscience Institute, University of Michigan, Ann Arbor, MI, USA. jclowney@umich.edu.

Rudy Behnia (R)

Department of Neuroscience, Columbia University, New York, NY, USA. rb3161@columbia.edu.
Zuckerman Institute, Columbia University, New York, NY, USA. rb3161@columbia.edu.
Kavli Institute for Brain Science, Columbia University, New York, NY, USA. rb3161@columbia.edu.

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