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Calbindin content and differential vulnerability of midbrain efferent dopaminergic neurons in macaques

Calbindin (CB) is a calcium binding protein reported to protect dopaminergic neurons from degeneration. Although a direct link between CB content and differential vulnerability of dopaminergic neurons has long been accepted, factors other than CB have also been suggested, particularly those related...

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Autores principales: Dopeso-Reyes, Iria G., Rico, Alberto J., Roda, Elvira, Sierra, Salvador, Pignataro, Diego, Lanz, Maria, Sucunza, Diego, Chang-Azancot, Luis, Lanciego, Jose L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4253956/
https://www.ncbi.nlm.nih.gov/pubmed/25520629
http://dx.doi.org/10.3389/fnana.2014.00146
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author Dopeso-Reyes, Iria G.
Rico, Alberto J.
Roda, Elvira
Sierra, Salvador
Pignataro, Diego
Lanz, Maria
Sucunza, Diego
Chang-Azancot, Luis
Lanciego, Jose L.
author_facet Dopeso-Reyes, Iria G.
Rico, Alberto J.
Roda, Elvira
Sierra, Salvador
Pignataro, Diego
Lanz, Maria
Sucunza, Diego
Chang-Azancot, Luis
Lanciego, Jose L.
author_sort Dopeso-Reyes, Iria G.
collection PubMed
description Calbindin (CB) is a calcium binding protein reported to protect dopaminergic neurons from degeneration. Although a direct link between CB content and differential vulnerability of dopaminergic neurons has long been accepted, factors other than CB have also been suggested, particularly those related to the dopamine transporter. Indeed, several studies have reported that CB levels are not causally related to the differential vulnerability of dopaminergic neurons against neurotoxins. Here we have used dual stains for tyrosine hydroxylase (TH) and CB in 3 control and 3 MPTP-treated monkeys to visualize dopaminergic neurons in the ventral tegmental area (VTA) and in the dorsal and ventral tiers of the substantia nigra pars compacta (SNcd and SNcv) co-expressing TH and CB. In control animals, the highest percentages of co-localization were found in VTA (58.2%), followed by neurons located in the SNcd (34.7%). As expected, SNcv neurons lacked CB expression. In MPTP-treated animals, the percentage of CB-ir/TH-ir neurons in the VTA was similar to control monkeys (62.1%), whereas most of the few surviving neurons in the SNcd were CB-ir/TH-ir (88.6%). Next, we have elucidated the presence of CB within identified nigrostriatal and nigroextrastriatal midbrain dopaminergic projection neurons. For this purpose, two control monkeys received one injection of Fluoro-Gold into the caudate nucleus and one injection of cholera toxin (CTB) into the postcommissural putamen, whereas two more monkeys were injected with CTB into the internal division of the globus pallidus (GPi). As expected, all the nigrocaudate- and nigroputamen-projecting neurons were TH-ir, although surprisingly, all of these nigrostriatal-projecting neurons were negative for CB. Furthermore, all the nigropallidal-projecting neurons co-expressed both TH and CB. In summary, although CB-ir dopaminergic neurons seem to be less prone to MPTP-induced degeneration, our data clearly demonstrated that these neurons are not giving rise to nigrostriatal projections and indeed CB-ir/TH-ir neurons only originate nigroextrastriatal projections.
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spelling pubmed-42539562014-12-17 Calbindin content and differential vulnerability of midbrain efferent dopaminergic neurons in macaques Dopeso-Reyes, Iria G. Rico, Alberto J. Roda, Elvira Sierra, Salvador Pignataro, Diego Lanz, Maria Sucunza, Diego Chang-Azancot, Luis Lanciego, Jose L. Front Neuroanat Neuroscience Calbindin (CB) is a calcium binding protein reported to protect dopaminergic neurons from degeneration. Although a direct link between CB content and differential vulnerability of dopaminergic neurons has long been accepted, factors other than CB have also been suggested, particularly those related to the dopamine transporter. Indeed, several studies have reported that CB levels are not causally related to the differential vulnerability of dopaminergic neurons against neurotoxins. Here we have used dual stains for tyrosine hydroxylase (TH) and CB in 3 control and 3 MPTP-treated monkeys to visualize dopaminergic neurons in the ventral tegmental area (VTA) and in the dorsal and ventral tiers of the substantia nigra pars compacta (SNcd and SNcv) co-expressing TH and CB. In control animals, the highest percentages of co-localization were found in VTA (58.2%), followed by neurons located in the SNcd (34.7%). As expected, SNcv neurons lacked CB expression. In MPTP-treated animals, the percentage of CB-ir/TH-ir neurons in the VTA was similar to control monkeys (62.1%), whereas most of the few surviving neurons in the SNcd were CB-ir/TH-ir (88.6%). Next, we have elucidated the presence of CB within identified nigrostriatal and nigroextrastriatal midbrain dopaminergic projection neurons. For this purpose, two control monkeys received one injection of Fluoro-Gold into the caudate nucleus and one injection of cholera toxin (CTB) into the postcommissural putamen, whereas two more monkeys were injected with CTB into the internal division of the globus pallidus (GPi). As expected, all the nigrocaudate- and nigroputamen-projecting neurons were TH-ir, although surprisingly, all of these nigrostriatal-projecting neurons were negative for CB. Furthermore, all the nigropallidal-projecting neurons co-expressed both TH and CB. In summary, although CB-ir dopaminergic neurons seem to be less prone to MPTP-induced degeneration, our data clearly demonstrated that these neurons are not giving rise to nigrostriatal projections and indeed CB-ir/TH-ir neurons only originate nigroextrastriatal projections. Frontiers Media S.A. 2014-12-03 /pmc/articles/PMC4253956/ /pubmed/25520629 http://dx.doi.org/10.3389/fnana.2014.00146 Text en Copyright © 2014 Dopeso-Reyes, Rico, Roda, Sierra, Pignataro, Lanz, Sucunza, Chang-Azancot and Lanciego. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Dopeso-Reyes, Iria G.
Rico, Alberto J.
Roda, Elvira
Sierra, Salvador
Pignataro, Diego
Lanz, Maria
Sucunza, Diego
Chang-Azancot, Luis
Lanciego, Jose L.
Calbindin content and differential vulnerability of midbrain efferent dopaminergic neurons in macaques
title Calbindin content and differential vulnerability of midbrain efferent dopaminergic neurons in macaques
title_full Calbindin content and differential vulnerability of midbrain efferent dopaminergic neurons in macaques
title_fullStr Calbindin content and differential vulnerability of midbrain efferent dopaminergic neurons in macaques
title_full_unstemmed Calbindin content and differential vulnerability of midbrain efferent dopaminergic neurons in macaques
title_short Calbindin content and differential vulnerability of midbrain efferent dopaminergic neurons in macaques
title_sort calbindin content and differential vulnerability of midbrain efferent dopaminergic neurons in macaques
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4253956/
https://www.ncbi.nlm.nih.gov/pubmed/25520629
http://dx.doi.org/10.3389/fnana.2014.00146
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