Characterization of aromatase expression in the adult male and female mouse brain. I. Coexistence with oestrogen receptors α and β, and androgen receptors.
Identifieur interne : 003792 ( PubMed/Curation ); précédent : 003791; suivant : 003793Characterization of aromatase expression in the adult male and female mouse brain. I. Coexistence with oestrogen receptors α and β, and androgen receptors.
Auteurs : Davor Stani [Australie] ; Sydney Dubois [France] ; Hui Kheng Chua [Australie] ; Bruce Tonge [Australie] ; Nicole Rinehart [Australie] ; Malcolm K. Horne [Australie] ; Wah Chin Boon [Australie]Source :
- PloS one [ 1932-6203 ] ; 2014.
Descripteurs français
- KwdFr :
- Animaux, Aromatase (génétique), Aromatase (métabolisme), Cartographie cérébrale, Encéphale (anatomie et histologie), Encéphale (métabolisme), Facteurs sexuels, Femelle, Gènes rapporteurs, Mâle, Protéines à fluorescence verte (génétique), Protéines à fluorescence verte (métabolisme), Récepteur alpha des oestrogènes (génétique), Récepteur alpha des oestrogènes (métabolisme), Récepteur bêta des oestrogènes (génétique), Récepteur bêta des oestrogènes (métabolisme), Récepteurs aux androgènes (génétique), Récepteurs aux androgènes (métabolisme), Régulation de l'expression des gènes, Souris, Souris transgéniques, Transcription génétique, Transduction du signal.
- MESH :
- anatomie et histologie : Encéphale.
- génétique : Aromatase, Protéines à fluorescence verte, Récepteur alpha des oestrogènes, Récepteur bêta des oestrogènes, Récepteurs aux androgènes.
- métabolisme : Aromatase, Encéphale, Protéines à fluorescence verte, Récepteur alpha des oestrogènes, Récepteur bêta des oestrogènes, Récepteurs aux androgènes.
- Animaux, Cartographie cérébrale, Facteurs sexuels, Femelle, Gènes rapporteurs, Mâle, Régulation de l'expression des gènes, Souris, Souris transgéniques, Transcription génétique, Transduction du signal.
English descriptors
- KwdEn :
- Animals, Aromatase (genetics), Aromatase (metabolism), Brain (anatomy & histology), Brain (metabolism), Brain Mapping, Estrogen Receptor alpha (genetics), Estrogen Receptor alpha (metabolism), Estrogen Receptor beta (genetics), Estrogen Receptor beta (metabolism), Female, Gene Expression Regulation, Genes, Reporter, Green Fluorescent Proteins (genetics), Green Fluorescent Proteins (metabolism), Male, Mice, Mice, Transgenic, Receptors, Androgen (genetics), Receptors, Androgen (metabolism), Sex Factors, Signal Transduction, Transcription, Genetic.
- MESH :
- chemical , genetics : Aromatase, Estrogen Receptor alpha, Estrogen Receptor beta, Green Fluorescent Proteins, Receptors, Androgen.
- chemical , metabolism : Aromatase, Estrogen Receptor alpha, Estrogen Receptor beta, Green Fluorescent Proteins, Receptors, Androgen.
- anatomy & histology : Brain.
- metabolism : Brain.
- Animals, Brain Mapping, Female, Gene Expression Regulation, Genes, Reporter, Male, Mice, Mice, Transgenic, Sex Factors, Signal Transduction, Transcription, Genetic.
Abstract
Aromatase catalyses the last step of oestrogen synthesis. There is growing evidence that local oestrogens influence many brain regions to modulate brain development and behaviour. We examined, by immunohistochemistry, the expression of aromatase in the adult male and female mouse brain, using mice in which enhanced green fluorescent protein (EGFP) is transcribed following the physiological activation of the Cyp19A1 gene. EGFP-immunoreactive processes were distributed in many brain regions, including the bed nucleus of the stria terminalis, olfactory tubercle, medial amygdaloid nucleus and medial preoptic area, with the densest distributions of EGFP-positive cell bodies in the bed nucleus and medial amygdala. Differences between male and female mice were apparent, with the density of EGFP-positive cell bodies and fibres being lower in some brain regions of female mice, including the bed nucleus and medial amygdala. EGFP-positive cell bodies in the bed nucleus, lateral septum, medial amygdala and hypothalamus co-expressed oestrogen receptor (ER) α and β, or the androgen receptor (AR), although single-labelled EGFP-positive cells were also identified. Additionally, single-labelled ERα-, ERβ- or AR-positive cell bodies often appeared to be surrounded by EGFP-immunoreactive nerve fibres/terminals. The widespread distribution of EGFP-positive cell bodies and fibres suggests that aromatase signalling is common in the mouse brain, and that locally synthesised brain oestrogens could mediate biological effects by activating pre- and post-synaptic oestrogen α and β receptors, and androgen receptors. The higher number of EGFP-positive cells in male mice may indicate that the autocrine and paracrine effects of oestrogens are more prominent in males than females.
DOI: 10.1371/journal.pone.0090451
PubMed: 24646567
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Department of Florey Neuroscience, University of Melbourne, Parkville, Victoria, Australia; Department of Anatomy and Developmental Biology, Monash University, Clayton, Victoria, Australia.</nlm:affiliation><country xml:lang="fr">Australie</country><wicri:regionArea>Neurodegeneration, The Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Victoria, Australia; Department of Florey Neuroscience, University of Melbourne, Parkville, Victoria, Australia; Department of Anatomy and Developmental Biology, Monash University, Clayton, Victoria</wicri:regionArea></affiliation></author></analytic><series><title level="j">PloS one</title><idno type="eISSN">1932-6203</idno><imprint><date when="2014" type="published">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term><term>Aromatase (genetics)</term><term>Aromatase (metabolism)</term><term>Brain (anatomy & histology)</term><term>Brain (metabolism)</term><term>Brain Mapping</term><term>Estrogen Receptor alpha (genetics)</term><term>Estrogen Receptor alpha (metabolism)</term><term>Estrogen Receptor beta (genetics)</term><term>Estrogen Receptor beta (metabolism)</term><term>Female</term><term>Gene Expression Regulation</term><term>Genes, Reporter</term><term>Green Fluorescent Proteins (genetics)</term><term>Green Fluorescent Proteins (metabolism)</term><term>Male</term><term>Mice</term><term>Mice, Transgenic</term><term>Receptors, Androgen (genetics)</term><term>Receptors, Androgen (metabolism)</term><term>Sex Factors</term><term>Signal Transduction</term><term>Transcription, Genetic</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Animaux</term><term>Aromatase (génétique)</term><term>Aromatase (métabolisme)</term><term>Cartographie cérébrale</term><term>Encéphale (anatomie et histologie)</term><term>Encéphale (métabolisme)</term><term>Facteurs sexuels</term><term>Femelle</term><term>Gènes rapporteurs</term><term>Mâle</term><term>Protéines à fluorescence verte (génétique)</term><term>Protéines à fluorescence verte (métabolisme)</term><term>Récepteur alpha des oestrogènes (génétique)</term><term>Récepteur alpha des oestrogènes (métabolisme)</term><term>Récepteur bêta des oestrogènes (génétique)</term><term>Récepteur bêta des oestrogènes (métabolisme)</term><term>Récepteurs aux androgènes (génétique)</term><term>Récepteurs aux androgènes (métabolisme)</term><term>Régulation de l'expression des gènes</term><term>Souris</term><term>Souris transgéniques</term><term>Transcription génétique</term><term>Transduction du signal</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Aromatase</term><term>Estrogen Receptor alpha</term><term>Estrogen Receptor beta</term><term>Green Fluorescent Proteins</term><term>Receptors, Androgen</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Aromatase</term><term>Estrogen Receptor alpha</term><term>Estrogen Receptor beta</term><term>Green Fluorescent Proteins</term><term>Receptors, Androgen</term></keywords><keywords scheme="MESH" qualifier="anatomie et histologie" xml:lang="fr"><term>Encéphale</term></keywords><keywords scheme="MESH" qualifier="anatomy & histology" xml:lang="en"><term>Brain</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Aromatase</term><term>Protéines à fluorescence verte</term><term>Récepteur alpha des oestrogènes</term><term>Récepteur bêta des oestrogènes</term><term>Récepteurs aux androgènes</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Brain</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Aromatase</term><term>Encéphale</term><term>Protéines à fluorescence verte</term><term>Récepteur alpha des oestrogènes</term><term>Récepteur bêta des oestrogènes</term><term>Récepteurs aux androgènes</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Brain Mapping</term><term>Female</term><term>Gene Expression Regulation</term><term>Genes, Reporter</term><term>Male</term><term>Mice</term><term>Mice, Transgenic</term><term>Sex Factors</term><term>Signal Transduction</term><term>Transcription, Genetic</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Animaux</term><term>Cartographie cérébrale</term><term>Facteurs sexuels</term><term>Femelle</term><term>Gènes rapporteurs</term><term>Mâle</term><term>Régulation de l'expression des gènes</term><term>Souris</term><term>Souris transgéniques</term><term>Transcription génétique</term><term>Transduction du signal</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Aromatase catalyses the last step of oestrogen synthesis. There is growing evidence that local oestrogens influence many brain regions to modulate brain development and behaviour. We examined, by immunohistochemistry, the expression of aromatase in the adult male and female mouse brain, using mice in which enhanced green fluorescent protein (EGFP) is transcribed following the physiological activation of the Cyp19A1 gene. EGFP-immunoreactive processes were distributed in many brain regions, including the bed nucleus of the stria terminalis, olfactory tubercle, medial amygdaloid nucleus and medial preoptic area, with the densest distributions of EGFP-positive cell bodies in the bed nucleus and medial amygdala. Differences between male and female mice were apparent, with the density of EGFP-positive cell bodies and fibres being lower in some brain regions of female mice, including the bed nucleus and medial amygdala. EGFP-positive cell bodies in the bed nucleus, lateral septum, medial amygdala and hypothalamus co-expressed oestrogen receptor (ER) α and β, or the androgen receptor (AR), although single-labelled EGFP-positive cells were also identified. Additionally, single-labelled ERα-, ERβ- or AR-positive cell bodies often appeared to be surrounded by EGFP-immunoreactive nerve fibres/terminals. The widespread distribution of EGFP-positive cell bodies and fibres suggests that aromatase signalling is common in the mouse brain, and that locally synthesised brain oestrogens could mediate biological effects by activating pre- and post-synaptic oestrogen α and β receptors, and androgen receptors. The higher number of EGFP-positive cells in male mice may indicate that the autocrine and paracrine effects of oestrogens are more prominent in males than females.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">24646567</PMID><DateCreated><Year>2014</Year><Month>03</Month><Day>20</Day></DateCreated><DateCompleted><Year>2014</Year><Month>12</Month><Day>23</Day></DateCompleted><DateRevised><Year>2017</Year><Month>02</Month><Day>20</Day></DateRevised><Article PubModel="Electronic-eCollection"><Journal><ISSN IssnType="Electronic">1932-6203</ISSN><JournalIssue CitedMedium="Internet"><Volume>9</Volume><Issue>3</Issue><PubDate><Year>2014</Year></PubDate></JournalIssue><Title>PloS one</Title><ISOAbbreviation>PLoS ONE</ISOAbbreviation></Journal><ArticleTitle>Characterization of aromatase expression in the adult male and female mouse brain. I. Coexistence with oestrogen receptors α and β, and androgen receptors.</ArticleTitle><Pagination><MedlinePgn>e90451</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1371/journal.pone.0090451</ELocationID><Abstract><AbstractText>Aromatase catalyses the last step of oestrogen synthesis. There is growing evidence that local oestrogens influence many brain regions to modulate brain development and behaviour. We examined, by immunohistochemistry, the expression of aromatase in the adult male and female mouse brain, using mice in which enhanced green fluorescent protein (EGFP) is transcribed following the physiological activation of the Cyp19A1 gene. EGFP-immunoreactive processes were distributed in many brain regions, including the bed nucleus of the stria terminalis, olfactory tubercle, medial amygdaloid nucleus and medial preoptic area, with the densest distributions of EGFP-positive cell bodies in the bed nucleus and medial amygdala. Differences between male and female mice were apparent, with the density of EGFP-positive cell bodies and fibres being lower in some brain regions of female mice, including the bed nucleus and medial amygdala. EGFP-positive cell bodies in the bed nucleus, lateral septum, medial amygdala and hypothalamus co-expressed oestrogen receptor (ER) α and β, or the androgen receptor (AR), although single-labelled EGFP-positive cells were also identified. Additionally, single-labelled ERα-, ERβ- or AR-positive cell bodies often appeared to be surrounded by EGFP-immunoreactive nerve fibres/terminals. The widespread distribution of EGFP-positive cell bodies and fibres suggests that aromatase signalling is common in the mouse brain, and that locally synthesised brain oestrogens could mediate biological effects by activating pre- and post-synaptic oestrogen α and β receptors, and androgen receptors. The higher number of EGFP-positive cells in male mice may indicate that the autocrine and paracrine effects of oestrogens are more prominent in males than females.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Stanić</LastName><ForeName>Davor</ForeName><Initials>D</Initials><AffiliationInfo><Affiliation>Systems Neurophysiology, The Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Victoria, Australia; Department of Florey Neuroscience, University of Melbourne, Parkville, Victoria, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Dubois</LastName><ForeName>Sydney</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>Neurodegeneration, The Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Victoria, Australia; Départment de Biologie, Ecole Normale Supérieure de Lyon, Lyon, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Chua</LastName><ForeName>Hui Kheng</ForeName><Initials>HK</Initials><AffiliationInfo><Affiliation>Neurodegeneration, The Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Victoria, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Tonge</LastName><ForeName>Bruce</ForeName><Initials>B</Initials><AffiliationInfo><Affiliation>Centre for Developmental Psychiatry & Psychology, Monash University, Clayton, Victoria, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Rinehart</LastName><ForeName>Nicole</ForeName><Initials>N</Initials><AffiliationInfo><Affiliation>Centre for Developmental Psychiatry & Psychology, Monash University, Clayton, Victoria, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Horne</LastName><ForeName>Malcolm K</ForeName><Initials>MK</Initials><AffiliationInfo><Affiliation>Neurodegeneration, The Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Victoria, Australia; Department of Florey Neuroscience, University of Melbourne, Parkville, Victoria, Australia; Neurology Department, St Vincent's Hospital, Fitzroy, Victoria, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Boon</LastName><ForeName>Wah Chin</ForeName><Initials>WC</Initials><AffiliationInfo><Affiliation>Neurodegeneration, The Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Victoria, Australia; Department of Florey Neuroscience, University of Melbourne, Parkville, Victoria, Australia; Department of Anatomy and Developmental Biology, Monash University, Clayton, Victoria, Australia.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2014</Year><Month>03</Month><Day>19</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>PLoS One</MedlineTA><NlmUniqueID>101285081</NlmUniqueID><ISSNLinking>1932-6203</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D047628">Estrogen Receptor alpha</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D047629">Estrogen Receptor beta</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D011944">Receptors, Androgen</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C485184">enhanced green fluorescent protein</NameOfSubstance></Chemical><Chemical><RegistryNumber>147336-22-9</RegistryNumber><NameOfSubstance UI="D049452">Green Fluorescent 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