Cargando…

Electrotonic Coupling in the Pituitary Supports the Hypothalamic-Pituitary-Gonadal Axis in a Sex Specific Manner

Gap junctions are present in many cell types throughout the animal kingdom and allow fast intercellular electrical and chemical communication between neighboring cells. Connexin-36 (Cx36), the major neuronal gap junction protein, synchronizes cellular activity in the brain, but also in other organs....

Descripción completa

Detalles Bibliográficos
Autores principales: Göngrich, Christina, García-González, Diego, Le Magueresse, Corentin, Roth, Lena C., Watanabe, Yasuhito, Burks, Deborah J., Grinevich, Valery, Monyer, Hannah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988985/
https://www.ncbi.nlm.nih.gov/pubmed/27587994
http://dx.doi.org/10.3389/fnmol.2016.00065
_version_ 1782448492244893696
author Göngrich, Christina
García-González, Diego
Le Magueresse, Corentin
Roth, Lena C.
Watanabe, Yasuhito
Burks, Deborah J.
Grinevich, Valery
Monyer, Hannah
author_facet Göngrich, Christina
García-González, Diego
Le Magueresse, Corentin
Roth, Lena C.
Watanabe, Yasuhito
Burks, Deborah J.
Grinevich, Valery
Monyer, Hannah
author_sort Göngrich, Christina
collection PubMed
description Gap junctions are present in many cell types throughout the animal kingdom and allow fast intercellular electrical and chemical communication between neighboring cells. Connexin-36 (Cx36), the major neuronal gap junction protein, synchronizes cellular activity in the brain, but also in other organs. Here we identify a sex-specific role for Cx36 within the hypothalamic-pituitary-gonadal (HPG) axis at the level of the anterior pituitary gland (AP). We show that Cx36 is expressed in gonadotropes of the AP sustaining their synchronous activity. Cx36 ablation affects the entire downstream HPG axis in females, but not in males. We demonstrate that Cx36-mediated coupling between gonadotropes in the AP supports gonadotropin-releasing hormone-induced secretion of luteinizing hormone. Furthermore, we provide evidence for negative feedback regulation of Cx36 expression in the AP by estradiol. We thus, conclude that hormonally-controlled plasticity of gap junction communication at the level of the AP constitutes an additional mechanism affecting female reproduction.
format Online
Article
Text
id pubmed-4988985
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-49889852016-09-01 Electrotonic Coupling in the Pituitary Supports the Hypothalamic-Pituitary-Gonadal Axis in a Sex Specific Manner Göngrich, Christina García-González, Diego Le Magueresse, Corentin Roth, Lena C. Watanabe, Yasuhito Burks, Deborah J. Grinevich, Valery Monyer, Hannah Front Mol Neurosci Neuroscience Gap junctions are present in many cell types throughout the animal kingdom and allow fast intercellular electrical and chemical communication between neighboring cells. Connexin-36 (Cx36), the major neuronal gap junction protein, synchronizes cellular activity in the brain, but also in other organs. Here we identify a sex-specific role for Cx36 within the hypothalamic-pituitary-gonadal (HPG) axis at the level of the anterior pituitary gland (AP). We show that Cx36 is expressed in gonadotropes of the AP sustaining their synchronous activity. Cx36 ablation affects the entire downstream HPG axis in females, but not in males. We demonstrate that Cx36-mediated coupling between gonadotropes in the AP supports gonadotropin-releasing hormone-induced secretion of luteinizing hormone. Furthermore, we provide evidence for negative feedback regulation of Cx36 expression in the AP by estradiol. We thus, conclude that hormonally-controlled plasticity of gap junction communication at the level of the AP constitutes an additional mechanism affecting female reproduction. Frontiers Media S.A. 2016-08-18 /pmc/articles/PMC4988985/ /pubmed/27587994 http://dx.doi.org/10.3389/fnmol.2016.00065 Text en Copyright © 2016 Göngrich, García-González, Le Magueresse, Roth, Watanabe, Burks, Grinevich and Monyer. 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 or 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
Göngrich, Christina
García-González, Diego
Le Magueresse, Corentin
Roth, Lena C.
Watanabe, Yasuhito
Burks, Deborah J.
Grinevich, Valery
Monyer, Hannah
Electrotonic Coupling in the Pituitary Supports the Hypothalamic-Pituitary-Gonadal Axis in a Sex Specific Manner
title Electrotonic Coupling in the Pituitary Supports the Hypothalamic-Pituitary-Gonadal Axis in a Sex Specific Manner
title_full Electrotonic Coupling in the Pituitary Supports the Hypothalamic-Pituitary-Gonadal Axis in a Sex Specific Manner
title_fullStr Electrotonic Coupling in the Pituitary Supports the Hypothalamic-Pituitary-Gonadal Axis in a Sex Specific Manner
title_full_unstemmed Electrotonic Coupling in the Pituitary Supports the Hypothalamic-Pituitary-Gonadal Axis in a Sex Specific Manner
title_short Electrotonic Coupling in the Pituitary Supports the Hypothalamic-Pituitary-Gonadal Axis in a Sex Specific Manner
title_sort electrotonic coupling in the pituitary supports the hypothalamic-pituitary-gonadal axis in a sex specific manner
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988985/
https://www.ncbi.nlm.nih.gov/pubmed/27587994
http://dx.doi.org/10.3389/fnmol.2016.00065
work_keys_str_mv AT gongrichchristina electrotoniccouplinginthepituitarysupportsthehypothalamicpituitarygonadalaxisinasexspecificmanner
AT garciagonzalezdiego electrotoniccouplinginthepituitarysupportsthehypothalamicpituitarygonadalaxisinasexspecificmanner
AT lemagueressecorentin electrotoniccouplinginthepituitarysupportsthehypothalamicpituitarygonadalaxisinasexspecificmanner
AT rothlenac electrotoniccouplinginthepituitarysupportsthehypothalamicpituitarygonadalaxisinasexspecificmanner
AT watanabeyasuhito electrotoniccouplinginthepituitarysupportsthehypothalamicpituitarygonadalaxisinasexspecificmanner
AT burksdeborahj electrotoniccouplinginthepituitarysupportsthehypothalamicpituitarygonadalaxisinasexspecificmanner
AT grinevichvalery electrotoniccouplinginthepituitarysupportsthehypothalamicpituitarygonadalaxisinasexspecificmanner
AT monyerhannah electrotoniccouplinginthepituitarysupportsthehypothalamicpituitarygonadalaxisinasexspecificmanner