Missi ng links in preeclampsia cell model systems of endothelial dysfunction

dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP
dc.contributor.authorVIANA-MATTIOLI, Sarah
dc.contributor.authorFONSECA-ALANIZ, Miriam Helena
dc.contributor.authorPINHEIRO-DE-SOUSA, Iguaracy
dc.contributor.authorKRIEGER, Jose Eduardo
dc.contributor.authorSANDRIM, Valeria Cristina
dc.date.accessioned2023-08-16T17:46:09Z
dc.date.available2023-08-16T17:46:09Z
dc.date.issued2023
dc.description.abstractPreeclampsia, one of the main hypertensive disorders of pregnancy, is associated with circulating factors released by the ischemic placenta accompanied by systemic endothelial dysfunction. The etiology of preeclampsia remains poorly understood although it is associated with high maternal and fetal mortality and increased cardiovascular disease risk. Most cell model systems used for studying endothelial dysfunction have not taken into account hemodynamic physical factors such as shear-stress forces which may prevent extrapolation of cell data to in vivo settings. We overview the role of hemodynamic forces in modulating endothelial cell function and discuss strategies to reproduce this biological characteristic in vitro to improve our understanding of endothelial dysfunction associated with preeclampsia.eng
dc.description.indexMEDLINE
dc.description.indexPubMed
dc.description.indexWoS
dc.description.indexScopus
dc.description.sponsorshipCoordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES/Brazil) [88887.604855/2021-00]
dc.description.sponsorshipConselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq/Brazil) [308504/2021-6, 408426/2021-7]
dc.description.sponsorshipFundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP/Brazil) [2019/07230-8, 2021/12010-7]
dc.identifier.citationTRENDS IN MOLECULAR MEDICINE, v.29, n.7, p.541-553, 2023
dc.identifier.doi10.1016/j.molmed.2023.04.003
dc.identifier.eissn1471-499X
dc.identifier.issn1471-4914
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/54623
dc.language.isoeng
dc.publisherCELL PRESSeng
dc.relation.ispartofTrends in Molecular Medicine
dc.rightsrestrictedAccesseng
dc.rights.holderCopyright CELL PRESSeng
dc.subject.othercirculating angiogenic factorseng
dc.subject.otherearly-onset preeclampsiaeng
dc.subject.otherplacental growth-factoreng
dc.subject.otherfree fetal dnaeng
dc.subject.otherantiangiogenic factorseng
dc.subject.othersoluble endoglineng
dc.subject.othervascular endotheliumeng
dc.subject.othermolecular-mechanismseng
dc.subject.othertrimester serumeng
dc.subject.otherin-vitroeng
dc.subject.wosBiochemistry & Molecular Biologyeng
dc.subject.wosCell Biologyeng
dc.subject.wosMedicine, Research & Experimentaleng
dc.titleMissi ng links in preeclampsia cell model systems of endothelial dysfunctioneng
dc.typearticleeng
dc.type.categoryrevieweng
dc.type.versionpublishedVersioneng
dspace.entity.typePublication
hcfmusp.author.externalSANDRIM, Valeria Cristina:Sao Paulo State Univ UNESP, Inst Biosci, Dept Biophys & Pharmacol, Botucatu, SP, Brazil
hcfmusp.citation.scopus1
hcfmusp.contributor.author-fmusphcSARAH VIANA MATTIOLI
hcfmusp.contributor.author-fmusphcMIRIAM HELENA FONSECA ALANIZ
hcfmusp.contributor.author-fmusphcIGUARACY PINHEIRO DE SOUSA
hcfmusp.contributor.author-fmusphcJOSE EDUARDO KRIEGER
hcfmusp.description.beginpage541
hcfmusp.description.endpage553
hcfmusp.description.issue7
hcfmusp.description.volume29
hcfmusp.origemWOS
hcfmusp.origem.pubmed37173223
hcfmusp.origem.scopus2-s2.0-85159085520
hcfmusp.origem.wosWOS:001027554200001
hcfmusp.publisher.cityCAMBRIDGEeng
hcfmusp.publisher.countryUSAeng
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