Cargando…
Quantified Coexpression Analysis of Central Amygdala Subpopulations
Molecular identification and characterization of fear controlling circuitries is a promising path towards developing targeted treatments of fear-related disorders. Three-color in situ hybridization analysis was used to determine whether somatostatin (SOM, Sst), neurotensin (NTS, Nts), corticotropin-...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5810038/ https://www.ncbi.nlm.nih.gov/pubmed/29445764 http://dx.doi.org/10.1523/ENEURO.0010-18.2018 |
_version_ | 1783299672891195392 |
---|---|
author | McCullough, Kenneth M. Morrison, Filomene G. Hartmann, Jakob Carlezon, William A. Ressler, Kerry J. |
author_facet | McCullough, Kenneth M. Morrison, Filomene G. Hartmann, Jakob Carlezon, William A. Ressler, Kerry J. |
author_sort | McCullough, Kenneth M. |
collection | PubMed |
description | Molecular identification and characterization of fear controlling circuitries is a promising path towards developing targeted treatments of fear-related disorders. Three-color in situ hybridization analysis was used to determine whether somatostatin (SOM, Sst), neurotensin (NTS, Nts), corticotropin-releasing factor (CRF, Crf), tachykinin 2 (TAC2, Tac2), protein kinase c-δ (PKC-δ, Prkcd), and dopamine receptor 2 (DRD2, Drd2) mRNA colocalize in male mouse amygdala neurons. Expression and colocalization was examined across capsular (CeC), lateral (CeL), and medial (CeM) compartments of the central amygdala. The greatest expression of Prkcd and Drd2 were found in CeC and CeL. Crf was expressed primarily in CeL, while Sst-, Nts-, and Tac2-expressing neurons were distributed between CeL and CeM. High levels of colocalization were identified between Sst, Nts, Crf, and Tac2 within the CeL, while little colocalization was detected between any mRNAs within the CeM. These findings provide a more detailed understanding of the molecular mechanisms that regulate the development and maintenance of fear and anxiety behaviors. |
format | Online Article Text |
id | pubmed-5810038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-58100382018-02-14 Quantified Coexpression Analysis of Central Amygdala Subpopulations McCullough, Kenneth M. Morrison, Filomene G. Hartmann, Jakob Carlezon, William A. Ressler, Kerry J. eNeuro New Research Molecular identification and characterization of fear controlling circuitries is a promising path towards developing targeted treatments of fear-related disorders. Three-color in situ hybridization analysis was used to determine whether somatostatin (SOM, Sst), neurotensin (NTS, Nts), corticotropin-releasing factor (CRF, Crf), tachykinin 2 (TAC2, Tac2), protein kinase c-δ (PKC-δ, Prkcd), and dopamine receptor 2 (DRD2, Drd2) mRNA colocalize in male mouse amygdala neurons. Expression and colocalization was examined across capsular (CeC), lateral (CeL), and medial (CeM) compartments of the central amygdala. The greatest expression of Prkcd and Drd2 were found in CeC and CeL. Crf was expressed primarily in CeL, while Sst-, Nts-, and Tac2-expressing neurons were distributed between CeL and CeM. High levels of colocalization were identified between Sst, Nts, Crf, and Tac2 within the CeL, while little colocalization was detected between any mRNAs within the CeM. These findings provide a more detailed understanding of the molecular mechanisms that regulate the development and maintenance of fear and anxiety behaviors. Society for Neuroscience 2018-02-06 /pmc/articles/PMC5810038/ /pubmed/29445764 http://dx.doi.org/10.1523/ENEURO.0010-18.2018 Text en Copyright © 2018 McCullough et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | New Research McCullough, Kenneth M. Morrison, Filomene G. Hartmann, Jakob Carlezon, William A. Ressler, Kerry J. Quantified Coexpression Analysis of Central Amygdala Subpopulations |
title | Quantified Coexpression Analysis of Central Amygdala Subpopulations |
title_full | Quantified Coexpression Analysis of Central Amygdala Subpopulations |
title_fullStr | Quantified Coexpression Analysis of Central Amygdala Subpopulations |
title_full_unstemmed | Quantified Coexpression Analysis of Central Amygdala Subpopulations |
title_short | Quantified Coexpression Analysis of Central Amygdala Subpopulations |
title_sort | quantified coexpression analysis of central amygdala subpopulations |
topic | New Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5810038/ https://www.ncbi.nlm.nih.gov/pubmed/29445764 http://dx.doi.org/10.1523/ENEURO.0010-18.2018 |
work_keys_str_mv | AT mcculloughkennethm quantifiedcoexpressionanalysisofcentralamygdalasubpopulations AT morrisonfilomeneg quantifiedcoexpressionanalysisofcentralamygdalasubpopulations AT hartmannjakob quantifiedcoexpressionanalysisofcentralamygdalasubpopulations AT carlezonwilliama quantifiedcoexpressionanalysisofcentralamygdalasubpopulations AT resslerkerryj quantifiedcoexpressionanalysisofcentralamygdalasubpopulations |