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Sex separation unveils the functional plasticity of the vomeronasal organ in rabbits
Chemosensory cues are vital for social and sexual behaviours and are primarily detected and processed by the vomeronasal system (VNS), whose plastic capacity has been investigated in mice. However, studying chemosensory plasticity outside of laboratory conditions may give a more realistic picture of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9634631/ https://www.ncbi.nlm.nih.gov/pubmed/36340690 http://dx.doi.org/10.3389/fnmol.2022.1034254 |
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author | Villamayor, Paula R. Gullón, Julián Quintela, Luis Sánchez-Quinteiro, Pablo Martínez, Paulino Robledo, Diego |
author_facet | Villamayor, Paula R. Gullón, Julián Quintela, Luis Sánchez-Quinteiro, Pablo Martínez, Paulino Robledo, Diego |
author_sort | Villamayor, Paula R. |
collection | PubMed |
description | Chemosensory cues are vital for social and sexual behaviours and are primarily detected and processed by the vomeronasal system (VNS), whose plastic capacity has been investigated in mice. However, studying chemosensory plasticity outside of laboratory conditions may give a more realistic picture of how the VNS adapts to a changing environment. Rabbits are a well-described model of chemocommunication since the discovery of the rabbit mammary pheromone and their vomeronasal organ (VNO) transcriptome was recently characterised, a first step to further study plasticity-mediated transcriptional changes. In this study, we assessed the plastic capacity of the rabbit male and female VNO under sex-separation vs. sex-combined scenarios, including adults and juveniles, to determine whether the rabbit VNO is plastic and, if so, whether such plasticity is already established at early stages of life. First, we characterised the number of differentially expressed genes (DEGs) between the VNO of rabbit male and female under sex-separation and compared it to sex-combined individuals, both in adults and juveniles, finding that differences between male and female were larger in a sex-separated scenario. Secondly, we analysed the number of DEGs between sex-separated and sex-combined scenarios, both in males and females. In adults, both sexes showed a high number of DEGs while in juveniles only females showed differences. Additionally, the vomeronasal receptor genes were strikingly downregulated in sex-separated adult females, whereas in juveniles upregulation was shown for the same condition, suggesting a role of VRs in puberty onset. Finally, we described the environment-modulated plastic capacity of genes involved in reproduction, immunity and VNO functional activity, including G-protein coupled receptors. Our results show that sex-separation induces sex- and stage-specific gene expression differences in the VNO of male and female rabbit, both in adults and juveniles. These results bring out for the first time the plastic capacity of the rabbit VNO, supporting its functional adaptation to specifically respond to a continuous changing environment. Finally, species-specific differences and individual variability should always be considered in VNO studies and overall chemocommunication research. |
format | Online Article Text |
id | pubmed-9634631 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96346312022-11-05 Sex separation unveils the functional plasticity of the vomeronasal organ in rabbits Villamayor, Paula R. Gullón, Julián Quintela, Luis Sánchez-Quinteiro, Pablo Martínez, Paulino Robledo, Diego Front Mol Neurosci Neuroscience Chemosensory cues are vital for social and sexual behaviours and are primarily detected and processed by the vomeronasal system (VNS), whose plastic capacity has been investigated in mice. However, studying chemosensory plasticity outside of laboratory conditions may give a more realistic picture of how the VNS adapts to a changing environment. Rabbits are a well-described model of chemocommunication since the discovery of the rabbit mammary pheromone and their vomeronasal organ (VNO) transcriptome was recently characterised, a first step to further study plasticity-mediated transcriptional changes. In this study, we assessed the plastic capacity of the rabbit male and female VNO under sex-separation vs. sex-combined scenarios, including adults and juveniles, to determine whether the rabbit VNO is plastic and, if so, whether such plasticity is already established at early stages of life. First, we characterised the number of differentially expressed genes (DEGs) between the VNO of rabbit male and female under sex-separation and compared it to sex-combined individuals, both in adults and juveniles, finding that differences between male and female were larger in a sex-separated scenario. Secondly, we analysed the number of DEGs between sex-separated and sex-combined scenarios, both in males and females. In adults, both sexes showed a high number of DEGs while in juveniles only females showed differences. Additionally, the vomeronasal receptor genes were strikingly downregulated in sex-separated adult females, whereas in juveniles upregulation was shown for the same condition, suggesting a role of VRs in puberty onset. Finally, we described the environment-modulated plastic capacity of genes involved in reproduction, immunity and VNO functional activity, including G-protein coupled receptors. Our results show that sex-separation induces sex- and stage-specific gene expression differences in the VNO of male and female rabbit, both in adults and juveniles. These results bring out for the first time the plastic capacity of the rabbit VNO, supporting its functional adaptation to specifically respond to a continuous changing environment. Finally, species-specific differences and individual variability should always be considered in VNO studies and overall chemocommunication research. Frontiers Media S.A. 2022-10-21 /pmc/articles/PMC9634631/ /pubmed/36340690 http://dx.doi.org/10.3389/fnmol.2022.1034254 Text en Copyright © 2022 Villamayor, Gullón, Quintela, Sánchez-Quinteiro, Martínez and Robledo. https://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 or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) 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 Villamayor, Paula R. Gullón, Julián Quintela, Luis Sánchez-Quinteiro, Pablo Martínez, Paulino Robledo, Diego Sex separation unveils the functional plasticity of the vomeronasal organ in rabbits |
title | Sex separation unveils the functional plasticity of the vomeronasal organ in rabbits |
title_full | Sex separation unveils the functional plasticity of the vomeronasal organ in rabbits |
title_fullStr | Sex separation unveils the functional plasticity of the vomeronasal organ in rabbits |
title_full_unstemmed | Sex separation unveils the functional plasticity of the vomeronasal organ in rabbits |
title_short | Sex separation unveils the functional plasticity of the vomeronasal organ in rabbits |
title_sort | sex separation unveils the functional plasticity of the vomeronasal organ in rabbits |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9634631/ https://www.ncbi.nlm.nih.gov/pubmed/36340690 http://dx.doi.org/10.3389/fnmol.2022.1034254 |
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