Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/109639
DC FieldValueLanguage
dc.contributor.authorCecchelli, Romeo-
dc.contributor.authorAday, Sezin-
dc.contributor.authorSevin, Emmanuel-
dc.contributor.authorAlmeida, Catarina-
dc.contributor.authorCulot, Maxime-
dc.contributor.authorDehouck, Lucie-
dc.contributor.authorCoisne, Caroline-
dc.contributor.authorEngelhardt, Britta-
dc.contributor.authorDehouck, Marie-Pierre-
dc.contributor.authorFerreira, Lino-
dc.date.accessioned2023-10-19T09:30:55Z-
dc.date.available2023-10-19T09:30:55Z-
dc.date.issued2014-
dc.identifier.issn1932-6203pt
dc.identifier.urihttps://hdl.handle.net/10316/109639-
dc.description.abstractThe human blood brain barrier (BBB) is a selective barrier formed by human brain endothelial cells (hBECs), which is important to ensure adequate neuronal function and protect the central nervous system (CNS) from disease. The development of human in vitro BBB models is thus of utmost importance for drug discovery programs related to CNS diseases. Here, we describe a method to generate a human BBB model using cord blood-derived hematopoietic stem cells. The cells were initially differentiated into ECs followed by the induction of BBB properties by co-culture with pericytes. The brain-like endothelial cells (BLECs) express tight junctions and transporters typically observed in brain endothelium and maintain expression of most in vivo BBB properties for at least 20 days. The model is very reproducible since it can be generated from stem cells isolated from different donors and in different laboratories, and could be used to predict CNS distribution of compounds in human. Finally, we provide evidence that Wnt/β-catenin signaling pathway mediates in part the BBB inductive properties of pericytes.pt
dc.description.sponsorshipThis work was supported by a Marie Curie-Reintegration Grant (FP7-People-2007-4-3-IRG; contract no 230929), funds of FEDER through the ‘‘Programa Operacional Factores de Competitividade- Compete’’ and Portuguese funds through FCT-Science and Technology Foundation (PTDC/CTM/099659/2008, PEst-C/ SAU/LA0001/2013–2014; and SFRH/BD/42871/2008, a fellowship to S.A.), COMPETE funding (Project ‘‘Stem cell based platforms for Regenerative and Therapeutic Medicine’’, Centro-07-ST24-FEDER-002008), FP7 (contracts 201024 and 202213 (European Stroke Network)) and PRIM (from the region Nord-Pas de Calais (France)).pt
dc.language.isoengpt
dc.publisherPublic Library of Sciencept
dc.relationPTDC/CTM/099659/2008pt
dc.relationPEst-C/SAU/LA0001/2013pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subject.meshBiomarkerspt
dc.subject.meshBlood-Brain Barrierpt
dc.subject.meshCapillary Permeabilitypt
dc.subject.meshCell Adhesion Moleculespt
dc.subject.meshCell Differentiationpt
dc.subject.meshCells, Culturedpt
dc.subject.meshCoculture Techniquespt
dc.subject.meshEndothelial Cellspt
dc.subject.meshEndothelium, Vascularpt
dc.subject.meshGene Expressionpt
dc.subject.meshHedgehog Proteinspt
dc.subject.meshHematopoietic Stem Cellspt
dc.subject.meshHumanspt
dc.subject.meshModels, Biologicalpt
dc.subject.meshPericytespt
dc.subject.meshReproducibility of Resultspt
dc.subject.meshWnt Signaling Pathwaypt
dc.titleA stable and reproducible human blood-brain barrier model derived from hematopoietic stem cellspt
dc.typearticle-
degois.publication.firstPagee99733pt
degois.publication.issue6pt
degois.publication.titlePLoS ONEpt
dc.peerreviewedyespt
dc.identifier.doi10.1371/journal.pone.0099733pt
degois.publication.volume9pt
dc.date.embargo2014-01-01*
uc.date.periodoEmbargo0pt
item.fulltextCom Texto completo-
item.grantfulltextopen-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.project.grantnoStrategic Project - LA 1 - 2013-2014-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0001-8985-9302-
Appears in Collections:IIIUC - Artigos em Revistas Internacionais
I&D CNC - Artigos em Revistas Internacionais
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