Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/12860

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Campo DCValorIdioma
dc.contributor.authorGomes, Sílvia C.-
dc.contributor.authorGallego-Llamas, Jabier-
dc.contributor.authorLeonor, I. B.-
dc.contributor.authorMano, J. F.-
dc.contributor.authorReis, R. L.-
dc.contributor.authorKaplan, David-
dc.date.accessioned2011-07-18T13:56:49Z-
dc.date.available2011-07-18T13:56:49Z-
dc.date.issued2012-
dc.identifier.issn1932-6254por
dc.identifier.urihttps://hdl.handle.net/1822/12860-
dc.description.abstractThe development of a new generation of multifunctional biomaterials is a continual goal for the field of materials science. The in vivo functional behaviour of a new fusion protein that combines the mechanical properties of spider silk with the antimicrobial properties of hepcidin was addressed in this study. This new chimeric protein, termed 6mer + hepcidin, fuses spider dragline consensus sequences (6mer) and the antimicrobial peptide hepcidin, as we have recently described, with retention of bactericidal activity and low cytotoxicity. In the present study, mouse subcutaneous implants were studied to access the in vivo biological response to 6mer + hepcidin, which were compared with controls of silk alone (6mer), polylactic–glycolic acid (PLGA) films and empty defects. Along with visual observations, flow cytometry and histology analyses were used to determine the number and type of inflammatory cells at the implantation site. The results show a mild to low inflammatory reaction to the implanted materials and no apparent differences between the 6mer + hepcidin films and the other experimental controls, demonstrating that the new fusion protein has good in vivo biocompatibility, while maintaining antibiotic function.por
dc.description.sponsorshipThe authors thank Dr Tírcia Santos for her advice on this paper. Sílvia Gomes thanks the Portuguese Foundation for Science and Technology (FCT) for providing a PhD grant (No. SFRH/BD/28603/2006). This work was carried out under the scope of: the European NoE EXPERTISSUES project (No. NMP3-CT-2004-500283); the FIND AND BIND project, funded by the agency EU–EC (FP7 programme); the FCT R&D project ProteoLight (No. PTDC/FIS/68517/2006), funded by the FCT agency; the Chimera project (No. PTDC/EBB-EBI/109093/2008), funded by the FCT agency; the NIH (Grant No. P41 EB002520) Tissue Engineering Resource Center; and the NIH (Grant Nos EB003210 and DE017207).por
dc.language.isoengpor
dc.publisherWileypor
dc.relationinfo:eu-repo/grantAgreement/FCT/FARH/SFRH%2FBD%2F28603%2F2006/PT-
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/229292/EU-
dc.relationinfo:eu-repo/grantAgreement/FCT/5876-PPCDTI/PTDC%2FFIS%2F68517%2F2006/PT-
dc.relationinfo:eu-repo/grantAgreement/FCT/5876-PPCDTI/PTDC%2FEBB-EBI%2F109093%2F2008/PT-
dc.rightsopenAccesspor
dc.subjectSpider silkpor
dc.subjectFACSpor
dc.subjectAntimicrobial activitypor
dc.subjectHepcidinpor
dc.subjectChimeric proteinpor
dc.subjectTissue engineeringpor
dc.subjectInflammatory responsepor
dc.titleBiological responses to spider silk - antibiotic fusion proteinpor
dc.typearticle-
dc.peerreviewedyespor
dc.relation.publisherversionhttp://dx.doi.org/10.1002/term.437por
oaire.citationStartPage356-
oaire.citationEndPage368-
oaire.citationIssue5por
oaire.citationTitleJournal of Tissue Engineering and Regenerative Medicinepor
oaire.citationVolume6-
dc.identifier.eissn1932-7005-
dc.identifier.doi10.1002/term.437-
dc.identifier.pmid22514077por
dc.subject.wosScience & Technologypor
sdum.journalJournal of Tissue Engineering and Regenerative Medicinepor
Aparece nas coleções:3B’s - Artigos em revistas/Papers in scientific journals

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