<div class="csl-bib-body">
<div class="csl-entry">Rothbauer, M., Patel, N., Gondola, H., Siwetz, M., Huppertz, B., & Ertl, P. (2017). A comparative study of five physiological key parameters between four different human trophoblast-derived cell lines. <i>Scientific Reports</i>. https://doi.org/10.1038/s41598-017-06364-z</div>
</div>
The human placenta plays a crucial role as the interface between mother and fetus. It represents a unique tissue that undergoes morphological as well as functional changes on the cellular and tissue level throughout pregnancy. To better understand how the placenta works, a variety of techniques has been developed to re-create this complex physiological barrier in vitro. However, due to the low availability of freshly isolated primary cells, choriocarcinoma cell lines remain the usual suspects as in vitro models for placental research. Here, we present a comparative study on the functional aspects of the choriocarcinoma cell lines BeWo, JAR and Jeg-3, as well as the first trimester trophoblast cell line ACH-3P as placental in vitro barrier models for endocrine and transport studies. Functional assays including tight junction immunostaining, sodium fluorescein retardation, trans epithelial resistance, glucose transport, hormone secretion as well as size-dependent polystyrene nanoparticle transport were performed using the four cell types to evaluate key functional parameters of each cell line to act a relevant in vitro placental barrier model.
en
dc.description.sponsorship
European Union’s Horizon 2020
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dc.language
English
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dc.language.iso
en
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dc.publisher
Springer Nature
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dc.relation.ispartof
Scientific Reports
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dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
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dc.title
A comparative study of five physiological key parameters between four different human trophoblast-derived cell lines
en
dc.type
Article
en
dc.type
Artikel
de
dc.rights.license
Creative Commons Namensnennung 4.0 International
de
dc.rights.license
Creative Commons Attribution 4.0 International
en
dc.contributor.affiliation
University of Vienna, Austria
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dc.contributor.affiliation
Medical University of Graz, Austria
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dc.contributor.affiliation
Medical University of Graz, Austria
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dc.relation.grantno
685817
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dc.rights.holder
The Author(s) 2017
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dc.type.category
Original Research Article
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tuw.journal.peerreviewed
true
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tuw.peerreviewed
true
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tuw.version
vor
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dcterms.isPartOf.title
Scientific Reports
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tuw.publication.orgunit
E164 - Institut für Chemische Technologien und Analytik
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tuw.publication.orgunit
E163 - Institut für Angewandte Synthesechemie
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tuw.publisher.doi
10.1038/s41598-017-06364-z
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dc.identifier.eissn
2045-2322
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dc.identifier.libraryid
AC15335639
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dc.description.numberOfPages
11
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dc.identifier.urn
urn:nbn:at:at-ubtuw:3-5406
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tuw.author.orcid
0000-0002-9928-3631
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tuw.author.orcid
0000-0002-7625-2445
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dc.rights.identifier
CC BY 4.0
de
dc.rights.identifier
CC BY 4.0
en
wb.sci
true
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item.languageiso639-1
en
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open
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Publications
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research article
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http://purl.org/coar/resource_type/c_2df8fbb1
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item.fulltext
with Fulltext
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item.openaccessfulltext
Open Access
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crisitem.author.dept
E163-03-1 - Forschungsgruppe Cell Chip
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crisitem.author.dept
University of Vienna
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crisitem.author.dept
TU Wien
-
crisitem.author.dept
Medical University of Graz
-
crisitem.author.dept
E610 - Vizerektorat Forschung und Innovation
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crisitem.author.orcid
0000-0002-7625-2445
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crisitem.author.parentorg
E163-03 - Forschungsbereich Organische und Biologische Chemie