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dc.contributor.authorZamprogno, Pauline
dc.contributor.authorWüthrich, Simon
dc.contributor.authorAchenbach, Sven
dc.contributor.authorThoma, Giuditta
dc.contributor.authorStucki, Janick D
dc.contributor.authorHobi, Nina
dc.contributor.authorSchneider-Daum, Nicole
dc.contributor.authorLehr, Claus-Michael
dc.contributor.authorHuwer, Hanno
dc.contributor.authorGeiser, Thomas
dc.contributor.authorSchmid, Ralph A
dc.contributor.authorGuenat, Olivier T
dc.date.accessioned2021-02-24T16:10:42Z
dc.date.available2021-02-24T16:10:42Z
dc.date.issued2021-02-05
dc.identifier.citationCommun Biol. 2021 Feb 5;4(1):168. doi: 10.1038/s42003-021-01695-0.en_US
dc.identifier.pmid33547387
dc.identifier.doi10.1038/s42003-021-01695-0
dc.identifier.urihttp://hdl.handle.net/10033/622753
dc.description.abstractThe air-blood barrier with its complex architecture and dynamic environment is difficult to mimic in vitro. Lung-on-a-chips enable mimicking the breathing movements using a thin, stretchable PDMS membrane. However, they fail to reproduce the characteristic alveoli network as well as the biochemical and physical properties of the alveolar basal membrane. Here, we present a lung-on-a-chip, based on a biological, stretchable and biodegradable membrane made of collagen and elastin, that emulates an array of tiny alveoli with in vivo-like dimensions. This membrane outperforms PDMS in many ways: it does not absorb rhodamine-B, is biodegradable, is created by a simple method, and can easily be tuned to modify its thickness, composition and stiffness. The air-blood barrier is reconstituted using primary lung alveolar epithelial cells from patients and primary lung endothelial cells. Typical alveolar epithelial cell markers are expressed, while the barrier properties are preserved for up to 3 weeks.en_US
dc.language.isoenen_US
dc.publisherNature Pulishing Groupen_US
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleSecond-generation lung-on-a-chip with an array of stretchable alveoli made with a biological membrane.en_US
dc.typeArticleen_US
dc.identifier.eissn2399-3642
dc.contributor.departmentHIPS, Helmholtz-Institut für Pharmazeutische Forschung Saarland, Universitätscampus E8.1 66123 Saarbrücken, Germany.en_US
dc.identifier.journalCommunications biologyen_US
dc.source.volume4
dc.source.issue1
dc.source.beginpage168
dc.source.endpage
refterms.dateFOA2021-02-24T16:10:43Z
dc.source.journaltitleCommunications biology
dc.source.countryEngland


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Attribution 4.0 International
Except where otherwise noted, this item's license is described as Attribution 4.0 International