Cargando…
Sparse genetically defined neurons refine the canonical role of periaqueductal gray columnar organization
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 c...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9224993/ https://www.ncbi.nlm.nih.gov/pubmed/35674316 http://dx.doi.org/10.7554/eLife.77115 |
_version_ | 1784733508388782080 |
---|---|
author | La-Vu, Mimi Q Sethi, Ekayana Maesta-Pereira, Sandra Schuette, Peter J Tobias, Brooke C Reis, Fernando MCV Wang, Weisheng Torossian, Anita Bishop, Amy Leonard, Saskia J Lin, Lilly Cahill, Catherine M Adhikari, Avishek |
author_facet | La-Vu, Mimi Q Sethi, Ekayana Maesta-Pereira, Sandra Schuette, Peter J Tobias, Brooke C Reis, Fernando MCV Wang, Weisheng Torossian, Anita Bishop, Amy Leonard, Saskia J Lin, Lilly Cahill, Catherine M Adhikari, Avishek |
author_sort | La-Vu, Mimi Q |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9224993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-92249932022-06-24 Sparse genetically defined neurons refine the canonical role of periaqueductal gray columnar organization La-Vu, Mimi Q Sethi, Ekayana Maesta-Pereira, Sandra Schuette, Peter J Tobias, Brooke C Reis, Fernando MCV Wang, Weisheng Torossian, Anita Bishop, Amy Leonard, Saskia J Lin, Lilly Cahill, Catherine M Adhikari, Avishek eLife Neuroscience 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. eLife Sciences Publications, Ltd 2022-06-08 /pmc/articles/PMC9224993/ /pubmed/35674316 http://dx.doi.org/10.7554/eLife.77115 Text en © 2022, La-Vu et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience La-Vu, Mimi Q Sethi, Ekayana Maesta-Pereira, Sandra Schuette, Peter J Tobias, Brooke C Reis, Fernando MCV Wang, Weisheng Torossian, Anita Bishop, Amy Leonard, Saskia J Lin, Lilly Cahill, Catherine M Adhikari, Avishek Sparse genetically defined neurons refine the canonical role of periaqueductal gray columnar organization |
title | Sparse genetically defined neurons refine the canonical role of periaqueductal gray columnar organization |
title_full | Sparse genetically defined neurons refine the canonical role of periaqueductal gray columnar organization |
title_fullStr | Sparse genetically defined neurons refine the canonical role of periaqueductal gray columnar organization |
title_full_unstemmed | Sparse genetically defined neurons refine the canonical role of periaqueductal gray columnar organization |
title_short | Sparse genetically defined neurons refine the canonical role of periaqueductal gray columnar organization |
title_sort | sparse genetically defined neurons refine the canonical role of periaqueductal gray columnar organization |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9224993/ https://www.ncbi.nlm.nih.gov/pubmed/35674316 http://dx.doi.org/10.7554/eLife.77115 |
work_keys_str_mv | AT lavumimiq sparsegeneticallydefinedneuronsrefinethecanonicalroleofperiaqueductalgraycolumnarorganization AT sethiekayana sparsegeneticallydefinedneuronsrefinethecanonicalroleofperiaqueductalgraycolumnarorganization AT maestapereirasandra sparsegeneticallydefinedneuronsrefinethecanonicalroleofperiaqueductalgraycolumnarorganization AT schuettepeterj sparsegeneticallydefinedneuronsrefinethecanonicalroleofperiaqueductalgraycolumnarorganization AT tobiasbrookec sparsegeneticallydefinedneuronsrefinethecanonicalroleofperiaqueductalgraycolumnarorganization AT reisfernandomcv sparsegeneticallydefinedneuronsrefinethecanonicalroleofperiaqueductalgraycolumnarorganization AT wangweisheng sparsegeneticallydefinedneuronsrefinethecanonicalroleofperiaqueductalgraycolumnarorganization AT torossiananita sparsegeneticallydefinedneuronsrefinethecanonicalroleofperiaqueductalgraycolumnarorganization AT bishopamy sparsegeneticallydefinedneuronsrefinethecanonicalroleofperiaqueductalgraycolumnarorganization AT leonardsaskiaj sparsegeneticallydefinedneuronsrefinethecanonicalroleofperiaqueductalgraycolumnarorganization AT linlilly sparsegeneticallydefinedneuronsrefinethecanonicalroleofperiaqueductalgraycolumnarorganization AT cahillcatherinem sparsegeneticallydefinedneuronsrefinethecanonicalroleofperiaqueductalgraycolumnarorganization AT adhikariavishek sparsegeneticallydefinedneuronsrefinethecanonicalroleofperiaqueductalgraycolumnarorganization |