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dc.contributor.authorBarrett, DW
dc.contributor.authorOkesola, BO
dc.contributor.authorCosta, E
dc.contributor.authorThrasivoulou, C
dc.contributor.authorBecker, DL
dc.contributor.authorMata, A
dc.contributor.authorDeprest, JA
dc.contributor.authorDavid, AL
dc.contributor.authorChowdhury, TT
dc.date.accessioned2020-11-19T10:13:12Z
dc.date.available2020-09-04
dc.date.available2020-11-19T10:13:12Z
dc.date.issued2020-10-12
dc.identifier.issn0197-3851
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/68492
dc.description.abstractObjective: We examined whether peptide amphiphiles functionalised with adhesive, migratory or regenerative sequences could be combined with amniotic fluid (AF) to form plugs that repair fetal membrane (FM) defects after trauma and co‐culture with connexin 43 (Cx43) antisense. Methods: We assessed interactions between peptide amphiphiles and AF and examined the plugs in FM defects after trauma and co‐culture with the Cx43antisense. Results: Confocal microscopy confirmed directed self‐assembly of peptide amphiphiles with AF to form a plug within minutes, with good mechanical properties. SEM of the plug revealed a multi‐layered, nanofibrous network that sealed the FM defect after trauma. Co‐culture of the FM defect with Cx43 antisense and plug increased collagen levels but reduced GAG. Culture of the FM defect with peptide amphiphiles incorporating regenerative sequences for 5 days, increased F‐actin and nuclear cell contraction, migration and polarization of collagen fibers across the FM defect when compared to control specimens with minimal repair. Conclusions: Whilst the nanoarchitecture revealed promising conditions to seal iatrogenic FM defects, the peptide amphiphiles need to be designed to maximize repair mechanisms and promote structural compliance with high mechanical tolerance that maintains tissue remodeling with Cx43 antisense for future treatment.en_US
dc.publisherPrenatal Diagnosis published by John Wiley & Sons Ltden_US
dc.relation.ispartofPRENATAL DIAGNOSIS
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.titlePotential sealing and repair of humanFMdefects after trauma with peptide amphiphiles and Cx43 antisenseen_US
dc.typeArticleen_US
dc.rights.holder© 2020 The Authors.
dc.identifier.doi10.1002/pd.5826
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000576728600001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Except where otherwise noted, this item's license is described as This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.