Sparse genetically defined neurons refine the canonical role of periaqueductal gray columnar organization.

cholecystokinin escape fear mouse neuroscience optogenetics periaqueductal gray predator

Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
08 06 2022
Historique:
received: 15 01 2022
accepted: 25 05 2022
pubmed: 9 6 2022
medline: 25 6 2022
entrez: 8 6 2022
Statut: epublish

Résumé

During threat exposure, survival depends on defensive reactions. Prior works linked large glutamatergic populations in the midbrain periaqueductal gray (PAG) to defensive freezing and flight, and established that the overarching functional organization axis of the PAG is along anatomically-defined columns. Accordingly, broad activation of the dorsolateral column induces flight, while activation of the lateral or ventrolateral (l and vl) columns induces freezing. However, the PAG contains diverse cell types that vary in neurochemistry. How these cell types contribute to defense remains unknown, indicating that targeting sparse, genetically-defined populations may reveal how the PAG generates diverse behaviors. Though prior works showed that broad excitation of the lPAG or vlPAG causes freezing, we found in mice that activation of lateral and ventrolateral PAG (l/vlPAG) cholecystokinin-expressing (CCK) cells selectively caused flight to safer regions within an environment. Furthermore, inhibition of l/vlPAG-CCK cells reduced predator avoidance without altering other defensive behaviors like freezing. Lastly, l/vlPAG-CCK activity decreased when approaching threat and increased during movement to safer locations. These results suggest CCK cells drive threat avoidance states, which are epochs during which mice increase distance from threat and perform evasive escape. Conversely, l/vlPAG pan-neuronal activation promoted freezing, and these cells were activated near threat. Thus, CCK l/vlPAG cells have opposing function and neural activation motifs compared to the broader local ensemble defined solely by columnar boundaries. In addition to the anatomical columnar architecture of the PAG, the molecular identity of PAG cells may confer an additional axis of functional organization, revealing unexplored functional heterogeneity.

Identifiants

pubmed: 35674316
doi: 10.7554/eLife.77115
pii: 77115
pmc: PMC9224993
doi:
pii:

Substances chimiques

Cholecystokinin 9011-97-6

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIMH NIH HHS
ID : F31 MH121050
Pays : United States
Organisme : NIMH NIH HHS
ID : R00 MH106649
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH119089
Pays : United States
Organisme : NIGMS NIH HHS
ID : R25 GM055052
Pays : United States

Informations de copyright

© 2022, La-Vu et al.

Déclaration de conflit d'intérêts

ML, ES, SM, PS, BT, FR, WW, AT, AB, SL, LL, CC, AA No competing interests declared

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Auteurs

Mimi Q La-Vu (MQ)

Neuroscience Interdepartmental Program, University of California, Los Angeles, Los Angeles, United States.
Department of Psychology, University of California, Los Angeles, Los Angeles, United States.

Ekayana Sethi (E)

Department of Psychology, University of California, Los Angeles, Los Angeles, United States.

Sandra Maesta-Pereira (S)

Department of Psychology, University of California, Los Angeles, Los Angeles, United States.

Peter J Schuette (PJ)

Neuroscience Interdepartmental Program, University of California, Los Angeles, Los Angeles, United States.
Department of Psychology, University of California, Los Angeles, Los Angeles, United States.

Brooke C Tobias (BC)

Department of Psychology, University of California, Los Angeles, Los Angeles, United States.

Fernando M C V Reis (FMCV)

Department of Psychology, University of California, Los Angeles, Los Angeles, United States.

Weisheng Wang (W)

Department of Psychology, University of California, Los Angeles, Los Angeles, United States.

Anita Torossian (A)

Neuroscience Interdepartmental Program, University of California, Los Angeles, Los Angeles, United States.
Department of Psychology, University of California, Los Angeles, Los Angeles, United States.

Amy Bishop (A)

Hatos Center for Neuropharmacology, University of California, Los Angeles, Los Angeles, United States.

Saskia J Leonard (SJ)

Department of Psychology, University of California, Los Angeles, Los Angeles, United States.

Lilly Lin (L)

Department of Psychology, University of California, Los Angeles, Los Angeles, United States.

Catherine M Cahill (CM)

Hatos Center for Neuropharmacology, University of California, Los Angeles, Los Angeles, United States.
Department of Psychiatry and Biobehavioral Sciences, Los Angeles, United States.
Semel Institute for Neuroscience and Human Behavior, Los Angeles, United States.

Avishek Adhikari (A)

Department of Psychology, University of California, Los Angeles, Los Angeles, United States.

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