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Cerebellum-Specific Deletion of the GABA(A) Receptor δ Subunit Leads to Sex-Specific Disruption of Behavior
Granule cells (GCs) of the cerebellar input layer express high-affinity δ GABA(A) subunit-containing GABA(A) receptors (δGABA(A)Rs) that respond to ambient GABA levels and context-dependent neuromodulators like steroids. We find that GC-specific deletion of δGABA(A) (cerebellar [cb] δ knockout [KO])...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700496/ https://www.ncbi.nlm.nih.gov/pubmed/33147470 http://dx.doi.org/10.1016/j.celrep.2020.108338 |
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author | Rudolph, Stephanie Guo, Chong Pashkovski, Stan L. Osorno, Tomas Gillis, Winthrop F. Krauss, Jeremy M. Nyitrai, Hajnalka Flaquer, Isabella El-Rifai, Mahmoud Datta, Sandeep Robert Regehr, Wade G. |
author_facet | Rudolph, Stephanie Guo, Chong Pashkovski, Stan L. Osorno, Tomas Gillis, Winthrop F. Krauss, Jeremy M. Nyitrai, Hajnalka Flaquer, Isabella El-Rifai, Mahmoud Datta, Sandeep Robert Regehr, Wade G. |
author_sort | Rudolph, Stephanie |
collection | PubMed |
description | Granule cells (GCs) of the cerebellar input layer express high-affinity δ GABA(A) subunit-containing GABA(A) receptors (δGABA(A)Rs) that respond to ambient GABA levels and context-dependent neuromodulators like steroids. We find that GC-specific deletion of δGABA(A) (cerebellar [cb] δ knockout [KO]) decreases tonic inhibition, makes GCs hyperexcitable, and in turn, leads to differential activation of cb output regions as well as many cortical and subcortical brain areas involved in cognition, anxiety-like behaviors, and the stress response. Cb δ KO mice display deficits in many behaviors, but motor function is normal. Strikingly, δGABA(A) deletion alters maternal behavior as well as spontaneous, stress-related, and social behaviors specifically in females. Our findings establish that δGABA(A)Rs enable the cerebellum to control diverse behaviors not previously associated with the cerebellum in a sex-dependent manner. These insights may contribute to a better understanding of the mechanisms that underlie behavioral abnormalities in psychiatric and neurodevelopmental disorders that display a gender bias. |
format | Online Article Text |
id | pubmed-7700496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-77004962020-11-29 Cerebellum-Specific Deletion of the GABA(A) Receptor δ Subunit Leads to Sex-Specific Disruption of Behavior Rudolph, Stephanie Guo, Chong Pashkovski, Stan L. Osorno, Tomas Gillis, Winthrop F. Krauss, Jeremy M. Nyitrai, Hajnalka Flaquer, Isabella El-Rifai, Mahmoud Datta, Sandeep Robert Regehr, Wade G. Cell Rep Article Granule cells (GCs) of the cerebellar input layer express high-affinity δ GABA(A) subunit-containing GABA(A) receptors (δGABA(A)Rs) that respond to ambient GABA levels and context-dependent neuromodulators like steroids. We find that GC-specific deletion of δGABA(A) (cerebellar [cb] δ knockout [KO]) decreases tonic inhibition, makes GCs hyperexcitable, and in turn, leads to differential activation of cb output regions as well as many cortical and subcortical brain areas involved in cognition, anxiety-like behaviors, and the stress response. Cb δ KO mice display deficits in many behaviors, but motor function is normal. Strikingly, δGABA(A) deletion alters maternal behavior as well as spontaneous, stress-related, and social behaviors specifically in females. Our findings establish that δGABA(A)Rs enable the cerebellum to control diverse behaviors not previously associated with the cerebellum in a sex-dependent manner. These insights may contribute to a better understanding of the mechanisms that underlie behavioral abnormalities in psychiatric and neurodevelopmental disorders that display a gender bias. 2020-11-03 /pmc/articles/PMC7700496/ /pubmed/33147470 http://dx.doi.org/10.1016/j.celrep.2020.108338 Text en This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Rudolph, Stephanie Guo, Chong Pashkovski, Stan L. Osorno, Tomas Gillis, Winthrop F. Krauss, Jeremy M. Nyitrai, Hajnalka Flaquer, Isabella El-Rifai, Mahmoud Datta, Sandeep Robert Regehr, Wade G. Cerebellum-Specific Deletion of the GABA(A) Receptor δ Subunit Leads to Sex-Specific Disruption of Behavior |
title | Cerebellum-Specific Deletion of the GABA(A) Receptor δ Subunit Leads to Sex-Specific Disruption of Behavior |
title_full | Cerebellum-Specific Deletion of the GABA(A) Receptor δ Subunit Leads to Sex-Specific Disruption of Behavior |
title_fullStr | Cerebellum-Specific Deletion of the GABA(A) Receptor δ Subunit Leads to Sex-Specific Disruption of Behavior |
title_full_unstemmed | Cerebellum-Specific Deletion of the GABA(A) Receptor δ Subunit Leads to Sex-Specific Disruption of Behavior |
title_short | Cerebellum-Specific Deletion of the GABA(A) Receptor δ Subunit Leads to Sex-Specific Disruption of Behavior |
title_sort | cerebellum-specific deletion of the gaba(a) receptor δ subunit leads to sex-specific disruption of behavior |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700496/ https://www.ncbi.nlm.nih.gov/pubmed/33147470 http://dx.doi.org/10.1016/j.celrep.2020.108338 |
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