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Does a third intermediate model for the vomeronasal processing of information exist? Insights from the macropodid neuroanatomy
The study of the α-subunit of Gi2 and Go proteins in the accessory olfactory bulb (AOB) was crucial for the identification of the two main families of vomeronasal receptors, V1R and V2R. Both families are expressed in the rodent and lagomorph AOBs, according to a segregated model characterized by to...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8930919/ https://www.ncbi.nlm.nih.gov/pubmed/34800143 http://dx.doi.org/10.1007/s00429-021-02425-2 |
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author | Torres, Mateo V. Ortiz-Leal, Irene Villamayor, Paula R. Ferreiro, Andrea Rois, José Luis Sanchez-Quinteiro, Pablo |
author_facet | Torres, Mateo V. Ortiz-Leal, Irene Villamayor, Paula R. Ferreiro, Andrea Rois, José Luis Sanchez-Quinteiro, Pablo |
author_sort | Torres, Mateo V. |
collection | PubMed |
description | The study of the α-subunit of Gi2 and Go proteins in the accessory olfactory bulb (AOB) was crucial for the identification of the two main families of vomeronasal receptors, V1R and V2R. Both families are expressed in the rodent and lagomorph AOBs, according to a segregated model characterized by topographical anteroposterior zonation. Many mammal species have suffered from the deterioration of the Gαo pathway and are categorized as belonging to the uniform model. This scenario has been complicated by characterization of the AOB in the tammar wallaby, Notamacropus eugenii, which appears to follow a third model of vomeronasal organization featuring exclusive Gαo protein expression, referred to as the intermediate model, which has not yet been replicated in any other species. Our morphofunctional study of the vomeronasal system (VNS) in Bennett’s wallaby, Notamacropus rufogriseus, provides further information regarding this third model of vomeronasal transduction. A comprehensive histological, lectin, and immunohistochemical study of the Bennett’s wallaby VNS was performed. Anti-Gαo and anti-Gαi2 antibodies were particularly useful because they labeled the transduction cascade of V2R and V1R receptors, respectively. Both G proteins showed canonical immunohistochemical labeling in the vomeronasal organ and the AOB, consistent with the anterior–posterior zonation of the segregated model. The lectin Ulex europaeus agglutinin selectively labeled the anterior AOB, providing additional evidence for the segregation of vomeronasal information in the wallaby. Overall, the VNS of the Bennett’s wallaby shows a degree of differentiation and histochemical and neurochemical diversity comparable to species with greater VNS development. The existence of the third intermediate type in vomeronasal information processing reported in Notamacropus eugenii is not supported by our lectin-histochemical and immunohistochemical findings in Notamacropus rufogriseus. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00429-021-02425-2. |
format | Online Article Text |
id | pubmed-8930919 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-89309192022-04-01 Does a third intermediate model for the vomeronasal processing of information exist? Insights from the macropodid neuroanatomy Torres, Mateo V. Ortiz-Leal, Irene Villamayor, Paula R. Ferreiro, Andrea Rois, José Luis Sanchez-Quinteiro, Pablo Brain Struct Funct Original Article The study of the α-subunit of Gi2 and Go proteins in the accessory olfactory bulb (AOB) was crucial for the identification of the two main families of vomeronasal receptors, V1R and V2R. Both families are expressed in the rodent and lagomorph AOBs, according to a segregated model characterized by topographical anteroposterior zonation. Many mammal species have suffered from the deterioration of the Gαo pathway and are categorized as belonging to the uniform model. This scenario has been complicated by characterization of the AOB in the tammar wallaby, Notamacropus eugenii, which appears to follow a third model of vomeronasal organization featuring exclusive Gαo protein expression, referred to as the intermediate model, which has not yet been replicated in any other species. Our morphofunctional study of the vomeronasal system (VNS) in Bennett’s wallaby, Notamacropus rufogriseus, provides further information regarding this third model of vomeronasal transduction. A comprehensive histological, lectin, and immunohistochemical study of the Bennett’s wallaby VNS was performed. Anti-Gαo and anti-Gαi2 antibodies were particularly useful because they labeled the transduction cascade of V2R and V1R receptors, respectively. Both G proteins showed canonical immunohistochemical labeling in the vomeronasal organ and the AOB, consistent with the anterior–posterior zonation of the segregated model. The lectin Ulex europaeus agglutinin selectively labeled the anterior AOB, providing additional evidence for the segregation of vomeronasal information in the wallaby. Overall, the VNS of the Bennett’s wallaby shows a degree of differentiation and histochemical and neurochemical diversity comparable to species with greater VNS development. The existence of the third intermediate type in vomeronasal information processing reported in Notamacropus eugenii is not supported by our lectin-histochemical and immunohistochemical findings in Notamacropus rufogriseus. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00429-021-02425-2. Springer Berlin Heidelberg 2021-11-20 2022 /pmc/articles/PMC8930919/ /pubmed/34800143 http://dx.doi.org/10.1007/s00429-021-02425-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Torres, Mateo V. Ortiz-Leal, Irene Villamayor, Paula R. Ferreiro, Andrea Rois, José Luis Sanchez-Quinteiro, Pablo Does a third intermediate model for the vomeronasal processing of information exist? Insights from the macropodid neuroanatomy |
title | Does a third intermediate model for the vomeronasal processing of information exist? Insights from the macropodid neuroanatomy |
title_full | Does a third intermediate model for the vomeronasal processing of information exist? Insights from the macropodid neuroanatomy |
title_fullStr | Does a third intermediate model for the vomeronasal processing of information exist? Insights from the macropodid neuroanatomy |
title_full_unstemmed | Does a third intermediate model for the vomeronasal processing of information exist? Insights from the macropodid neuroanatomy |
title_short | Does a third intermediate model for the vomeronasal processing of information exist? Insights from the macropodid neuroanatomy |
title_sort | does a third intermediate model for the vomeronasal processing of information exist? insights from the macropodid neuroanatomy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8930919/ https://www.ncbi.nlm.nih.gov/pubmed/34800143 http://dx.doi.org/10.1007/s00429-021-02425-2 |
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