Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/92393
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dc.contributor.authorFerreira, Lino-
dc.date.accessioned2021-01-02T15:16:12Z-
dc.date.available2021-01-02T15:16:12Z-
dc.date.issued2019-
dc.identifier.issn1746-0441pt
dc.identifier.issn1746-045Xpt
dc.identifier.urihttps://hdl.handle.net/10316/92393-
dc.description.abstractIntroduction: Human in vitro blood-brain barrier (BBB) models could be important tools for studying BBB development, maintenance and regulation. However, our capacity to obtain information from these models is still limited in part because only in recent years have (i) these models been derived from non-brain cell sources (e.g. stem cells), (ii) microfluidic systems been developed to recapitulate aspects of BBB physiology and (iii) new insights into the molecular and cellular mechanisms of BBB diseases (e.g. Huntington´s, Allan-Herndon-Dudley Syndrome) been described. Area covered: This article reviews the technological advances in the derivation of human cells from the neurovascular unit using stem cells and the creation of personalized BBB models generated from patients with neurodegenerative diseases. It also reviews the scientific advances generated from in vitro BBB models. Expert opinion: The recent technological advances in the derivation of human cells from the neurovascular unit from stem cells as well as in the generation of BBB-on-a-chip that recapitulate in vitro part of the BBB physiology are significant to generate more robust BBB models; however, a considerable effort is still needed to validate the potential of these models to recapitulate the in vivo cellular and molecular mechanisms, in particular regarding BBB function in health and disease.pt
dc.description.sponsorshipThis work was funded by FEDER through the Program COMPETE and by Portuguese fund through FCT in context of the projects “AGING-MODEL” (Ref. POCI-01-0145- FEDER-029229) and “Unraveling the Rules of Passive Permeation Through the Blood-Brain Barrier” (Ref: PTDC/DTP-FTO/2784/2014), as well as the European project ERAatUC (ref. 669088). LF would like to thank Dr. Hugo Fernandes for the critical reading of the manuscript-
dc.language.isoengpt
dc.publisherTaylor & Francispt
dc.rightsopenAccesspt
dc.subjectBBB function; Blood-brain barrier (BBB); drug discovery; human models; stem cellspt
dc.subject.meshAnimalspt
dc.subject.meshBlood-Brain Barrierpt
dc.subject.meshBrain Diseasespt
dc.subject.meshDrug Discoverypt
dc.subject.meshHumanspt
dc.subject.meshLab-On-A-Chip Devicespt
dc.subject.meshModels, Biologicalpt
dc.subject.meshNeurodegenerative Diseasespt
dc.subject.meshStem Cellspt
dc.titleWhat human blood-brain barrier models can tell us about BBB function and drug discovery?pt
dc.typearticle-
degois.publication.firstPage1113-1123pt
degois.publication.lastPage1123pt
degois.publication.issue11pt
degois.publication.titleExpert Opinion on Drug Discoverypt
dc.peerreviewedyespt
dc.identifier.doi10.1080/17460441.2019.1646722pt
degois.publication.volume14pt
dc.date.embargo2019-01-01*
uc.date.periodoEmbargo0pt
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.languageiso639-1en-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0001-8985-9302-
Appears in Collections:UC Bibliotecas - Artigos em Revistas Internacionais
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