Specific retinal neurons regulate context-dependent defensive responses to visual threat.

defensive responses environmental context retinal ganglion cells shelter visual threat

Journal

PNAS nexus
ISSN: 2752-6542
Titre abrégé: PNAS Nexus
Pays: England
ID NLM: 9918367777906676

Informations de publication

Date de publication:
Oct 2024
Historique:
received: 07 05 2024
accepted: 10 09 2024
medline: 3 10 2024
pubmed: 3 10 2024
entrez: 3 10 2024
Statut: epublish

Résumé

While encountering a visual threat, an animal assesses multiple factors to choose an appropriate defensive strategy. For example, when a rodent detects a looming aerial predator, its behavioral response can be influenced by a specific environmental context, such as the availability of a shelter. Indeed, rodents typically escape from a looming stimulus when a shelter is present; otherwise, they typically freeze. Here we report that context-dependent behavioral responses can be initiated at the earliest stage of the visual system by distinct types of retinal ganglion cells (RGCs), the retina's output neurons. Using genetically defined cell ablation in mature mice, we discovered that some RGC types were necessary for either escaping (alpha RGCs) or freezing (intrinsically photosensitive RGCs) in response to a looming stimulus but not for both behaviors; whereas other RGC types were not required for either behavior (direction-selective RGCs preferring vertical motion). Altogether, our results suggest that specific RGC types regulate distinct behavioral responses elicited by the same threatening stimulus depending on contextual signals in the environment. These findings emphasize the unique contribution of early visual pathways to evolutionally conserved behavioral reactions.

Identifiants

pubmed: 39359403
doi: 10.1093/pnasnexus/pgae423
pii: pgae423
pmc: PMC11443969
doi:

Types de publication

Journal Article

Langues

eng

Pagination

pgae423

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of National Academy of Sciences.

Auteurs

Tracy Lee (T)

Department of Ophthalmology and Visual Science, Yale University School of Medicine, New Haven, CT 06511, USA.

Hannah Weinberg-Wolf (H)

Department of Ophthalmology and Visual Science, Yale University School of Medicine, New Haven, CT 06511, USA.

Thomas E Zapadka (TE)

Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, CT 06511, USA.

Andrii Rudenko (A)

Department of Biology, Graduate Programs in Biology and Biochemistry, City College and City University of New York, New York, NY 10031, USA.

Jonathan B Demb (JB)

Department of Ophthalmology and Visual Science, Yale University School of Medicine, New Haven, CT 06511, USA.
Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, CT 06511, USA.
Department of Neuroscience, Yale University School of Medicine, New Haven, CT 06511, USA.
Wu Tsai Institute, Yale University, New Haven, CT 06511, USA.

In-Jung Kim (IJ)

Department of Ophthalmology and Visual Science, Yale University School of Medicine, New Haven, CT 06511, USA.
Department of Neuroscience, Yale University School of Medicine, New Haven, CT 06511, USA.
Wu Tsai Institute, Yale University, New Haven, CT 06511, USA.

Classifications MeSH