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Glutamate neurons are intermixed with midbrain dopamine neurons in nonhuman primates and humans
The rodent ventral tegmental area (VTA) and substantia nigra pars compacta (SNC) contain dopamine neurons intermixed with glutamate neurons (expressing vesicular glutamate transporter 2; VGluT2), which play roles in reward and aversion. However, identifying the neuronal compositions of the VTA and S...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967922/ https://www.ncbi.nlm.nih.gov/pubmed/27477243 http://dx.doi.org/10.1038/srep30615 |
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author | Root, David H. Wang, Hui-Ling Liu, Bing Barker, David J. Mód, László Szocsics, Péter Silva, Afonso C. Maglóczky, Zsófia Morales, Marisela |
author_facet | Root, David H. Wang, Hui-Ling Liu, Bing Barker, David J. Mód, László Szocsics, Péter Silva, Afonso C. Maglóczky, Zsófia Morales, Marisela |
author_sort | Root, David H. |
collection | PubMed |
description | The rodent ventral tegmental area (VTA) and substantia nigra pars compacta (SNC) contain dopamine neurons intermixed with glutamate neurons (expressing vesicular glutamate transporter 2; VGluT2), which play roles in reward and aversion. However, identifying the neuronal compositions of the VTA and SNC in higher mammals has remained challenging. Here, we revealed VGluT2 neurons within the VTA and SNC of nonhuman primates and humans by simultaneous detection of VGluT2 mRNA and tyrosine hydroxylase (TH; for identification of dopamine neurons). We found that several VTA subdivisions share similar cellular compositions in nonhuman primates and humans; their rostral linear nuclei have a high prevalence of VGluT2 neurons lacking TH; their paranigral and parabrachial pigmented nuclei have mostly TH neurons, and their parabrachial pigmented nuclei have dual VGluT2-TH neurons. Within nonhuman primates and humans SNC, the vast majority of neurons are TH neurons but VGluT2 neurons were detected in the pars lateralis subdivision. The demonstration that midbrain dopamine neurons are intermixed with glutamate or glutamate-dopamine neurons from rodents to humans offers new opportunities for translational studies towards analyzing the roles that each of these neurons play in human behavior and in midbrain-associated illnesses such as addiction, depression, schizophrenia, and Parkinson’s disease. |
format | Online Article Text |
id | pubmed-4967922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49679222016-08-10 Glutamate neurons are intermixed with midbrain dopamine neurons in nonhuman primates and humans Root, David H. Wang, Hui-Ling Liu, Bing Barker, David J. Mód, László Szocsics, Péter Silva, Afonso C. Maglóczky, Zsófia Morales, Marisela Sci Rep Article The rodent ventral tegmental area (VTA) and substantia nigra pars compacta (SNC) contain dopamine neurons intermixed with glutamate neurons (expressing vesicular glutamate transporter 2; VGluT2), which play roles in reward and aversion. However, identifying the neuronal compositions of the VTA and SNC in higher mammals has remained challenging. Here, we revealed VGluT2 neurons within the VTA and SNC of nonhuman primates and humans by simultaneous detection of VGluT2 mRNA and tyrosine hydroxylase (TH; for identification of dopamine neurons). We found that several VTA subdivisions share similar cellular compositions in nonhuman primates and humans; their rostral linear nuclei have a high prevalence of VGluT2 neurons lacking TH; their paranigral and parabrachial pigmented nuclei have mostly TH neurons, and their parabrachial pigmented nuclei have dual VGluT2-TH neurons. Within nonhuman primates and humans SNC, the vast majority of neurons are TH neurons but VGluT2 neurons were detected in the pars lateralis subdivision. The demonstration that midbrain dopamine neurons are intermixed with glutamate or glutamate-dopamine neurons from rodents to humans offers new opportunities for translational studies towards analyzing the roles that each of these neurons play in human behavior and in midbrain-associated illnesses such as addiction, depression, schizophrenia, and Parkinson’s disease. Nature Publishing Group 2016-08-01 /pmc/articles/PMC4967922/ /pubmed/27477243 http://dx.doi.org/10.1038/srep30615 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Root, David H. Wang, Hui-Ling Liu, Bing Barker, David J. Mód, László Szocsics, Péter Silva, Afonso C. Maglóczky, Zsófia Morales, Marisela Glutamate neurons are intermixed with midbrain dopamine neurons in nonhuman primates and humans |
title | Glutamate neurons are intermixed with midbrain dopamine neurons in nonhuman primates and humans |
title_full | Glutamate neurons are intermixed with midbrain dopamine neurons in nonhuman primates and humans |
title_fullStr | Glutamate neurons are intermixed with midbrain dopamine neurons in nonhuman primates and humans |
title_full_unstemmed | Glutamate neurons are intermixed with midbrain dopamine neurons in nonhuman primates and humans |
title_short | Glutamate neurons are intermixed with midbrain dopamine neurons in nonhuman primates and humans |
title_sort | glutamate neurons are intermixed with midbrain dopamine neurons in nonhuman primates and humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967922/ https://www.ncbi.nlm.nih.gov/pubmed/27477243 http://dx.doi.org/10.1038/srep30615 |
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