Cargando…

Sexually dimorphic oxytocin receptor-expressing neurons in the preoptic area of the mouse brain

Oxytocin is involved in the regulation of social behaviors including parental behaviors in a variety of species. Oxytocin triggers social behaviors by binding to oxytocin receptors (OXTRs) in various parts of the brain. OXTRs are present in the preoptic area (POA) where hormone-sensitive sexually di...

Descripción completa

Detalles Bibliográficos
Autores principales: Sharma, Kaustubh, LeBlanc, Ryan, Haque, Masudul, Nishimori, Katsuhiko, Reid, Madigan M., Teruyama, Ryoichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6622548/
https://www.ncbi.nlm.nih.gov/pubmed/31295328
http://dx.doi.org/10.1371/journal.pone.0219784
_version_ 1783434174830477312
author Sharma, Kaustubh
LeBlanc, Ryan
Haque, Masudul
Nishimori, Katsuhiko
Reid, Madigan M.
Teruyama, Ryoichi
author_facet Sharma, Kaustubh
LeBlanc, Ryan
Haque, Masudul
Nishimori, Katsuhiko
Reid, Madigan M.
Teruyama, Ryoichi
author_sort Sharma, Kaustubh
collection PubMed
description Oxytocin is involved in the regulation of social behaviors including parental behaviors in a variety of species. Oxytocin triggers social behaviors by binding to oxytocin receptors (OXTRs) in various parts of the brain. OXTRs are present in the preoptic area (POA) where hormone-sensitive sexually dimorphic nuclei exist. The present study was conducted to examine whether sex differences exist in the distribution of neurons expressing OXTRs in the POA. Using OXTR-Venus (an enhanced variant of yellow fluorescent protein) mice, the distribution of OXTR-Venus cells in the POA was compared between sexes. The total number of OXTR-Venus cells in the medial POA (MPOA) was significantly greater in females than in males. No detectable OXTR-Venus cells were observed in the anteroventral periventricular nucleus (AVPV) within the MPOA in most of the brain sections from males. We further examined the total number of OXTR-Venus cells in the AVPV and the rest of the MPOA between the sexes. The total number of OXTR-Venus cells in the AVPV in females (615 ± 43) was significantly greater than that in males (14 ± 2), whereas the total number of OXTR-Venus cells in the rest of the MPOA did not differ significantly between the sexes. Thus, the sexually dimorphic expression of OXTR-Venus specifically occurred in the AVPV, but not in the rest of the MPOA. We also examined whether the expression of OXTR in the AVPV is driven by the female gonadal hormone, estrogen. Immunocytochemistry and single-cell RT-PCR revealed the presence of the estrogen receptor α in OXTR-Venus cells in the female AVPV. Moreover, ovariectomy resulted in the absence of OXTR-Venus expression in the AVPV, whereas estrogen replacement therapy restored OXTR-Venus expression. These results demonstrate that the expression of OXTR in the AVPV is primarily female specific and estrogen dependent. The presence of the sexually dimorphic expression of OXTR in the AVPV suggests the involvement of OXTR neurons in the AVPV in the regulation of female-specific behavior and/or physiology.
format Online
Article
Text
id pubmed-6622548
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-66225482019-07-25 Sexually dimorphic oxytocin receptor-expressing neurons in the preoptic area of the mouse brain Sharma, Kaustubh LeBlanc, Ryan Haque, Masudul Nishimori, Katsuhiko Reid, Madigan M. Teruyama, Ryoichi PLoS One Research Article Oxytocin is involved in the regulation of social behaviors including parental behaviors in a variety of species. Oxytocin triggers social behaviors by binding to oxytocin receptors (OXTRs) in various parts of the brain. OXTRs are present in the preoptic area (POA) where hormone-sensitive sexually dimorphic nuclei exist. The present study was conducted to examine whether sex differences exist in the distribution of neurons expressing OXTRs in the POA. Using OXTR-Venus (an enhanced variant of yellow fluorescent protein) mice, the distribution of OXTR-Venus cells in the POA was compared between sexes. The total number of OXTR-Venus cells in the medial POA (MPOA) was significantly greater in females than in males. No detectable OXTR-Venus cells were observed in the anteroventral periventricular nucleus (AVPV) within the MPOA in most of the brain sections from males. We further examined the total number of OXTR-Venus cells in the AVPV and the rest of the MPOA between the sexes. The total number of OXTR-Venus cells in the AVPV in females (615 ± 43) was significantly greater than that in males (14 ± 2), whereas the total number of OXTR-Venus cells in the rest of the MPOA did not differ significantly between the sexes. Thus, the sexually dimorphic expression of OXTR-Venus specifically occurred in the AVPV, but not in the rest of the MPOA. We also examined whether the expression of OXTR in the AVPV is driven by the female gonadal hormone, estrogen. Immunocytochemistry and single-cell RT-PCR revealed the presence of the estrogen receptor α in OXTR-Venus cells in the female AVPV. Moreover, ovariectomy resulted in the absence of OXTR-Venus expression in the AVPV, whereas estrogen replacement therapy restored OXTR-Venus expression. These results demonstrate that the expression of OXTR in the AVPV is primarily female specific and estrogen dependent. The presence of the sexually dimorphic expression of OXTR in the AVPV suggests the involvement of OXTR neurons in the AVPV in the regulation of female-specific behavior and/or physiology. Public Library of Science 2019-07-11 /pmc/articles/PMC6622548/ /pubmed/31295328 http://dx.doi.org/10.1371/journal.pone.0219784 Text en © 2019 Sharma et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Sharma, Kaustubh
LeBlanc, Ryan
Haque, Masudul
Nishimori, Katsuhiko
Reid, Madigan M.
Teruyama, Ryoichi
Sexually dimorphic oxytocin receptor-expressing neurons in the preoptic area of the mouse brain
title Sexually dimorphic oxytocin receptor-expressing neurons in the preoptic area of the mouse brain
title_full Sexually dimorphic oxytocin receptor-expressing neurons in the preoptic area of the mouse brain
title_fullStr Sexually dimorphic oxytocin receptor-expressing neurons in the preoptic area of the mouse brain
title_full_unstemmed Sexually dimorphic oxytocin receptor-expressing neurons in the preoptic area of the mouse brain
title_short Sexually dimorphic oxytocin receptor-expressing neurons in the preoptic area of the mouse brain
title_sort sexually dimorphic oxytocin receptor-expressing neurons in the preoptic area of the mouse brain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6622548/
https://www.ncbi.nlm.nih.gov/pubmed/31295328
http://dx.doi.org/10.1371/journal.pone.0219784
work_keys_str_mv AT sharmakaustubh sexuallydimorphicoxytocinreceptorexpressingneuronsinthepreopticareaofthemousebrain
AT leblancryan sexuallydimorphicoxytocinreceptorexpressingneuronsinthepreopticareaofthemousebrain
AT haquemasudul sexuallydimorphicoxytocinreceptorexpressingneuronsinthepreopticareaofthemousebrain
AT nishimorikatsuhiko sexuallydimorphicoxytocinreceptorexpressingneuronsinthepreopticareaofthemousebrain
AT reidmadiganm sexuallydimorphicoxytocinreceptorexpressingneuronsinthepreopticareaofthemousebrain
AT teruyamaryoichi sexuallydimorphicoxytocinreceptorexpressingneuronsinthepreopticareaofthemousebrain