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Transcriptome signature of the adult mouse choroid plexus

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Resumo:Background: Although the gene expression profile of several tissues in humans and in rodent animal models has been explored, analysis of the complete choroid plexus (CP) transcriptome is still lacking. A better characterization of the CP transcriptome can provide key insights into its functions as one of the barriers that separate the brain from the periphery and in the production of cerebrospinal fluid. Methods: This work extends further what is known about the mouse CP transcriptome through a microarray analysis of CP tissue from normal mice under physiological conditions. Results: We found that the genes most highly expressed are those implicated in energy metabolism (oxidative phosphorylation, glycolysis/gluconeogenesis) and in ribosomal function, which is in agreement with the secretory nature of the CP. On the other hand, genes encoding for immune mediators are among those with lower expression in basal conditions. In addition, we found genes known to be relevant during brain development, and not previously identified to be expressed in the CP, including those encoding for various axonal guidance and angiogenesis molecules and for growth factors. Some of these are known to influence the neural stem cell niche in the subventricular zone, highlighting the involvement of the CP as a likely modulator of neurogenesis. Interestingly, our observations confirm that the CP transcriptome is unique, displaying low homology with that of other tissues. Of note, we describe here that the closest similarity is with the transcriptome of the endothelial cells of the blood-brain barrier. Conclusions: Based on the data presented here, it will now be possible to further explore the function of particular proteins of the CP secretome in health and in disease.
Autores principais:Marques, Fernanda Cristina Gomes de Sousa
Outros Autores:Sousa, João Carlos; Coppola, Giovanni; Gao, Fuying; Puga, Renato; Brentani, Helena; Geschwind, Daniel H.; Sousa, Nuno; Neves, Margarida Correia; Palha, Joana Almeida
Assunto:Choroid plexus Basal transcriptome Mice
Ano:2011
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso aberto
Instituição associada:Universidade do Minho
Idioma:inglês
Origem:RepositóriUM - Universidade do Minho
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author Marques, Fernanda Cristina Gomes de Sousa
author2 Sousa, João Carlos
Coppola, Giovanni
Gao, Fuying
Puga, Renato
Brentani, Helena
Geschwind, Daniel H.
Sousa, Nuno
Neves, Margarida Correia
Palha, Joana Almeida
author2_role author
author
author
author
author
author
author
author
author
author_facet Marques, Fernanda Cristina Gomes de Sousa
Sousa, João Carlos
Coppola, Giovanni
Gao, Fuying
Puga, Renato
Brentani, Helena
Geschwind, Daniel H.
Sousa, Nuno
Neves, Margarida Correia
Palha, Joana Almeida
author_role author
contributor_name_str_mv RepositóriUM - Universidade do Minho
country_str PT
creators_json_txt [{\"Person.name\":\"Marques, Fernanda Cristina Gomes de Sousa\"},{\"Person.name\":\"Sousa, João Carlos\"},{\"Person.name\":\"Coppola, Giovanni\"},{\"Person.name\":\"Gao, Fuying\"},{\"Person.name\":\"Puga, Renato\"},{\"Person.name\":\"Brentani, Helena\"},{\"Person.name\":\"Geschwind, Daniel H.\"},{\"Person.name\":\"Sousa, Nuno\"},{\"Person.name\":\"Neves, Margarida Correia\"},{\"Person.name\":\"Palha, Joana Almeida\"}]
datacite.contributors.contributor.contributorName.fl_str_mv RepositóriUM - Universidade do Minho
datacite.creators.creator.creatorName.fl_str_mv Marques, Fernanda Cristina Gomes de Sousa
Sousa, João Carlos
Coppola, Giovanni
Gao, Fuying
Puga, Renato
Brentani, Helena
Geschwind, Daniel H.
Sousa, Nuno
Neves, Margarida Correia
Palha, Joana Almeida
datacite.date.Accepted.fl_str_mv 2011-01-01T00:00:00Z
datacite.rights.fl_str_mv http://purl.org/coar/access_right/c_abf2
datacite.subjects.subject.fl_str_mv Choroid plexus
Basal transcriptome
Mice
datacite.titles.title.fl_str_mv Transcriptome signature of the adult mouse choroid plexus
dc.contributor.none.fl_str_mv RepositóriUM - Universidade do Minho
dc.creator.none.fl_str_mv Marques, Fernanda Cristina Gomes de Sousa
Sousa, João Carlos
Coppola, Giovanni
Gao, Fuying
Puga, Renato
Brentani, Helena
Geschwind, Daniel H.
Sousa, Nuno
Neves, Margarida Correia
Palha, Joana Almeida
dc.date.Accepted.fl_str_mv 2011-01-01T00:00:00Z
dc.format.none.fl_str_mv application/pdf
dc.identifier.none.fl_str_mv https://hdl.handle.net/1822/16938
dc.language.none.fl_str_mv eng
dc.publisher.none.fl_str_mv BioMed Central (BMC)
dc.rights.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.subject.none.fl_str_mv Choroid plexus
Basal transcriptome
Mice
dc.title.fl_str_mv Transcriptome signature of the adult mouse choroid plexus
dc.type.none.fl_str_mv http://purl.org/coar/resource_type/c_6501
description Background: Although the gene expression profile of several tissues in humans and in rodent animal models has been explored, analysis of the complete choroid plexus (CP) transcriptome is still lacking. A better characterization of the CP transcriptome can provide key insights into its functions as one of the barriers that separate the brain from the periphery and in the production of cerebrospinal fluid. Methods: This work extends further what is known about the mouse CP transcriptome through a microarray analysis of CP tissue from normal mice under physiological conditions. Results: We found that the genes most highly expressed are those implicated in energy metabolism (oxidative phosphorylation, glycolysis/gluconeogenesis) and in ribosomal function, which is in agreement with the secretory nature of the CP. On the other hand, genes encoding for immune mediators are among those with lower expression in basal conditions. In addition, we found genes known to be relevant during brain development, and not previously identified to be expressed in the CP, including those encoding for various axonal guidance and angiogenesis molecules and for growth factors. Some of these are known to influence the neural stem cell niche in the subventricular zone, highlighting the involvement of the CP as a likely modulator of neurogenesis. Interestingly, our observations confirm that the CP transcriptome is unique, displaying low homology with that of other tissues. Of note, we describe here that the closest similarity is with the transcriptome of the endothelial cells of the blood-brain barrier. Conclusions: Based on the data presented here, it will now be possible to further explore the function of particular proteins of the CP secretome in health and in disease.
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eu_rights_str_mv openAccess
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id rum_f4fcabfcfb4acef1f6e7f3dfdde2e76d
identifier.url.fl_str_mv https://hdl.handle.net/1822/16938
inst_facet_str urn:organizationAcronym:repositorium{{{_:::_}}}Universidade do Minho
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institution Universidade do Minho
instname_str Universidade do Minho
language eng
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oai_identifier_str oai:repositorium.uminho.pt:1822/16938
organization_str_mv urn:organizationAcronym:repositorium
person_str_mv Marques, Fernanda Cristina Gomes de Sousa
Sousa, João Carlos
Coppola, Giovanni
Gao, Fuying
Puga, Renato
Brentani, Helena
Geschwind, Daniel H.
Sousa, Nuno
Neves, Margarida Correia
Palha, Joana Almeida
publishDate 2011
publisher.none.fl_str_mv BioMed Central (BMC)
repo_facet_str urn:repositoryAcronym:rum{{{_:::_}}}RepositóriUM - Universidade do Minho
reponame_str RepositóriUM - Universidade do Minho
repository_id_str urn:repositoryAcronym:rum
service_str_mv urn:repositoryAcronym:rum
spelling engBioMed Central (BMC)porBackground: Although the gene expression profile of several tissues in humans and in rodent animal models has been explored, analysis of the complete choroid plexus (CP) transcriptome is still lacking. A better characterization of the CP transcriptome can provide key insights into its functions as one of the barriers that separate the brain from the periphery and in the production of cerebrospinal fluid. Methods: This work extends further what is known about the mouse CP transcriptome through a microarray analysis of CP tissue from normal mice under physiological conditions. Results: We found that the genes most highly expressed are those implicated in energy metabolism (oxidative phosphorylation, glycolysis/gluconeogenesis) and in ribosomal function, which is in agreement with the secretory nature of the CP. On the other hand, genes encoding for immune mediators are among those with lower expression in basal conditions. In addition, we found genes known to be relevant during brain development, and not previously identified to be expressed in the CP, including those encoding for various axonal guidance and angiogenesis molecules and for growth factors. Some of these are known to influence the neural stem cell niche in the subventricular zone, highlighting the involvement of the CP as a likely modulator of neurogenesis. Interestingly, our observations confirm that the CP transcriptome is unique, displaying low homology with that of other tissues. Of note, we describe here that the closest similarity is with the transcriptome of the endothelial cells of the blood-brain barrier. Conclusions: Based on the data presented here, it will now be possible to further explore the function of particular proteins of the CP secretome in health and in disease.application/pdfporTranscriptome signature of the adult mouse choroid plexusMarques, Fernanda Cristina Gomes de SousaSousa, João CarlosCoppola, GiovanniGao, FuyingPuga, RenatoBrentani, HelenaGeschwind, Daniel H.Sousa, NunoNeves, Margarida CorreiaPalha, Joana AlmeidaHostingInstitutionOrganizationalRepositóriUM - Universidade do Minhoe-mailmailto:repositorium@usdb.uminho.ptrepositorium@usdb.uminho.ptISSNIsPartOf2045-8118DOIIsPartOf10.1186/2045-8118-8-102011-012011-01-01T00:00:00ZHandlehttps://hdl.handle.net/1822/16938http://purl.org/coar/access_right/c_abf2open accessChoroid plexusBasal transcriptomeMice1338786 bytesliteraturehttp://purl.org/coar/resource_type/c_6501journal articlehttp://purl.org/coar/access_right/c_abf2application/pdfhttps://repositorium.uminho.pt/bitstreams/b5b178bc-a94f-4395-9e6e-acfb3867719f/download
spellingShingle Transcriptome signature of the adult mouse choroid plexus
Marques, Fernanda Cristina Gomes de Sousa
Choroid plexus
Basal transcriptome
Mice
status SINGLETON
subject.fl_str_mv Choroid plexus
Basal transcriptome
Mice
title Transcriptome signature of the adult mouse choroid plexus
title_full Transcriptome signature of the adult mouse choroid plexus
title_fullStr Transcriptome signature of the adult mouse choroid plexus
title_full_unstemmed Transcriptome signature of the adult mouse choroid plexus
title_short Transcriptome signature of the adult mouse choroid plexus
title_sort Transcriptome signature of the adult mouse choroid plexus
topic Choroid plexus
Basal transcriptome
Mice
topic_facet Choroid plexus
Basal transcriptome
Mice
url https://hdl.handle.net/1822/16938
visible 1

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