Estrogen receptor-α signaling in tanycytes ...
Type de document :
Article dans une revue scientifique: Article original
PMID :
URL permanente :
Titre :
Estrogen receptor-α signaling in tanycytes lies at the crossroads of fertility and metabolism
Auteur(s) :
Fernandois, Daniela [Auteur]
Lille Neurosciences & Cognition - U 1172 [LilNCog]
Rusidze, Mariam [Auteur]
Mueller-Fielitz, Helge [Auteur]
Sauve, Florent [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Deligia, Eleonora [Auteur]
Lille Neurosciences & Cognition - U 1172 [LilNCog]
Mauro, Silva [Auteur]
Lille Neurosciences & Cognition - U 1172 [LilNCog]
Evrard, Florence [Auteur]
Lille Neurosciences & Cognition - U 1172 [LilNCog]
Franco-García, Aurelio [Auteur]
Mazur, Daniele [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Martinez Corral, Ines [Auteur]
Lille Neurosciences & Cognition - U 1172 [LilNCog]
Jouy, Nathalie [Auteur]
Plateformes Lilloises en Biologie et Santé (PLBS) - UAR 2014 - US 41
Rasika, Sowmyalakshmi [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Maurage, Claude-Alain [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Giacobini, Paolo [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Nogueiras, Ruben [Auteur]
Dehouck, Benedicte [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Schwaninger, Markus [Auteur]
Lenfant, Francoise [Auteur]
Prevot, Vincent [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Lille Neurosciences & Cognition - U 1172 [LilNCog]
Rusidze, Mariam [Auteur]
Mueller-Fielitz, Helge [Auteur]
Sauve, Florent [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Deligia, Eleonora [Auteur]
Lille Neurosciences & Cognition - U 1172 [LilNCog]
Mauro, Silva [Auteur]
Lille Neurosciences & Cognition - U 1172 [LilNCog]
Evrard, Florence [Auteur]
Lille Neurosciences & Cognition - U 1172 [LilNCog]
Franco-García, Aurelio [Auteur]
Mazur, Daniele [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Martinez Corral, Ines [Auteur]
Lille Neurosciences & Cognition - U 1172 [LilNCog]
Jouy, Nathalie [Auteur]
Plateformes Lilloises en Biologie et Santé (PLBS) - UAR 2014 - US 41
Rasika, Sowmyalakshmi [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Maurage, Claude-Alain [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Giacobini, Paolo [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Nogueiras, Ruben [Auteur]
Dehouck, Benedicte [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Schwaninger, Markus [Auteur]
Lenfant, Francoise [Auteur]
Prevot, Vincent [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Titre de la revue :
Metabolism
Nom court de la revue :
Metabolism
Numéro :
158
Pagination :
155976
Éditeur :
Elsevier
Date de publication :
2024-07-15
ISSN :
1532-8600
Mot(s)-clé(s) en anglais :
Estrogens
Tanycytes
LH pulsatility
Female metabolism
Reproduction
Hypothalamus
Tanycytes
LH pulsatility
Female metabolism
Reproduction
Hypothalamus
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
Background
Estrogen secretion by the ovaries regulates the hypothalamic-pituitary-gonadal axis during the reproductive cycle, influencing gonadotropin-releasing hormone (GnRH) and luteinizing hormone (LH) secretion, and ...
Lire la suite >Background Estrogen secretion by the ovaries regulates the hypothalamic-pituitary-gonadal axis during the reproductive cycle, influencing gonadotropin-releasing hormone (GnRH) and luteinizing hormone (LH) secretion, and also plays a role in regulating metabolism. Here, we establish that hypothalamic tanycytes—specialized glia lining the floor and walls of the third ventricle—integrate estrogenic feedback signals from the gonads and couple reproduction with metabolism by relaying this information to orexigenic neuropeptide Y (NPY) neurons. Methods Using mouse models, including mice floxed for Esr1 (encoding estrogen receptor alpha, ERα) and those with Cre-dependent expression of designer receptors exclusively activated by designer drugs (DREADDs), along with viral-mediated, pharmacological and indirect calorimetric approaches, we evaluated the role of tanycytes and tanycytic estrogen signaling in pulsatile LH secretion, cFos expression in NPY neurons, estrous cyclicity, body-weight changes and metabolic parameters in adult females. Results In ovariectomized mice, chemogenetic activation of tanycytes significantly reduced LH pulsatile release, mimicking the effects of direct NPY neuron activation. In intact mice, tanycytes were crucial for the estrogen-mediated control of GnRH/LH release, with tanycytic ERα activation suppressing fasting-induced NPY neuron activation. Selective knockout of Esr1 in tanycytes altered estrous cyclicity and fertility in female mice and affected estrogen's ability to inhibit refeeding in fasting mice. The absence of ERα signaling in tanycytes increased Npy transcripts and body weight in intact mice and prevented the estrogen-mediated decrease in food intake as well as increase in energy expenditure and fatty acid oxidation in ovariectomized mice. Conclusions Our findings underscore the pivotal role of tanycytes in the neuroendocrine coupling of reproduction and metabolism, with potential implications for its age-related deregulation after menopause. Significance statement Our investigation reveals that tanycytes, specialized glial cells in the brain, are key interpreters of estrogen signals for orexigenic NPY neurons in the hypothalamus. Disrupting tanycytic estrogen receptors not only alters fertility in female mice but also impairs the ability of estrogens to suppress appetite. This work thus sheds light on the critical role played by tanycytes in bridging the hormonal regulation of cyclic reproductive function and appetite/feeding behavior. This understanding may have potential implications for age-related metabolic deregulation after menopause.Lire moins >
Lire la suite >Background Estrogen secretion by the ovaries regulates the hypothalamic-pituitary-gonadal axis during the reproductive cycle, influencing gonadotropin-releasing hormone (GnRH) and luteinizing hormone (LH) secretion, and also plays a role in regulating metabolism. Here, we establish that hypothalamic tanycytes—specialized glia lining the floor and walls of the third ventricle—integrate estrogenic feedback signals from the gonads and couple reproduction with metabolism by relaying this information to orexigenic neuropeptide Y (NPY) neurons. Methods Using mouse models, including mice floxed for Esr1 (encoding estrogen receptor alpha, ERα) and those with Cre-dependent expression of designer receptors exclusively activated by designer drugs (DREADDs), along with viral-mediated, pharmacological and indirect calorimetric approaches, we evaluated the role of tanycytes and tanycytic estrogen signaling in pulsatile LH secretion, cFos expression in NPY neurons, estrous cyclicity, body-weight changes and metabolic parameters in adult females. Results In ovariectomized mice, chemogenetic activation of tanycytes significantly reduced LH pulsatile release, mimicking the effects of direct NPY neuron activation. In intact mice, tanycytes were crucial for the estrogen-mediated control of GnRH/LH release, with tanycytic ERα activation suppressing fasting-induced NPY neuron activation. Selective knockout of Esr1 in tanycytes altered estrous cyclicity and fertility in female mice and affected estrogen's ability to inhibit refeeding in fasting mice. The absence of ERα signaling in tanycytes increased Npy transcripts and body weight in intact mice and prevented the estrogen-mediated decrease in food intake as well as increase in energy expenditure and fatty acid oxidation in ovariectomized mice. Conclusions Our findings underscore the pivotal role of tanycytes in the neuroendocrine coupling of reproduction and metabolism, with potential implications for its age-related deregulation after menopause. Significance statement Our investigation reveals that tanycytes, specialized glial cells in the brain, are key interpreters of estrogen signals for orexigenic NPY neurons in the hypothalamus. Disrupting tanycytic estrogen receptors not only alters fertility in female mice but also impairs the ability of estrogens to suppress appetite. This work thus sheds light on the critical role played by tanycytes in bridging the hormonal regulation of cyclic reproductive function and appetite/feeding behavior. This understanding may have potential implications for age-related metabolic deregulation after menopause.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Projet Européen :
Établissement(s) :
Université de Lille
CHU Lille
CNRS
Inserm
Institut Pasteur de Lille
CHU Lille
CNRS
Inserm
Institut Pasteur de Lille
Collections :
Équipe(s) de recherche :
Développement et plasticité du cerveau neuro-endocrine
Date de dépôt :
2024-11-27T22:08:07Z
2024-12-13T14:28:52Z
2024-12-13T14:28:52Z
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