Silk Hydrogel Substrate Stress Relaxation Primes Mesenchymal Stem Cell Behavior in 2D

dc.bibliographicCitation.firstPage30420eng
dc.bibliographicCitation.issue26eng
dc.bibliographicCitation.journalTitleACS Applied Materials and Interfaceseng
dc.bibliographicCitation.lastPage30433eng
dc.bibliographicCitation.volume13eng
dc.contributor.authorPhuagkhaopong, Suttinee
dc.contributor.authorMendes, Luís
dc.contributor.authorMüller, Katrin
dc.contributor.authorWobus, Manja
dc.contributor.authorBornhäuser, Martin
dc.contributor.authorCarswell, Hilary V.O.
dc.contributor.authorDuarte, Iola F.
dc.contributor.authorSeib, F. Philipp
dc.date.accessioned2021-11-18T14:14:33Z
dc.date.available2021-11-18T14:14:33Z
dc.date.issued2021
dc.description.abstractTissue-mimetic silk hydrogels are being explored for diverse healthcare applications, including stem cell delivery. However, the impact of stress relaxation of silk hydrogels on human mesenchymal stem cell (MSC) biology is poorly defined. The aim of this study was to fabricate silk hydrogels with tuned mechanical properties that allowed the regulation of MSC biology in two dimensions. The silk content and stiffness of both elastic and viscoelastic silk hydrogels were kept constant to permit direct comparisons. Gene expression of IL-1β, IL-6, LIF, BMP-6, BMP-7, and protein tyrosine phosphatase receptor type C were substantially higher in MSCs cultured on elastic hydrogels than those on viscoelastic hydrogels, whereas this pattern was reversed for insulin, HNF-1A, and SOX-2. Protein expression was also mechanosensitive and the elastic cultures showed strong activation of IL-1β signaling in response to hydrogel mechanics. An elastic substrate also induced higher consumption of glucose and aspartate, coupled with a higher secretion of lactate, than was observed in MSCs grown on viscoelastic substrate. However, both silk hydrogels changed the magnitude of consumption of glucose, pyruvate, glutamine, and aspartate, and also metabolite secretion, resulting in an overall lower metabolic activity than that found in control cells. Together, these findings describe how stress relaxation impacts the overall biology of MSCs cultured on silk hydrogels. ©eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/7358
dc.identifier.urihttps://doi.org/10.34657/6405
dc.language.isoengeng
dc.publisherWashington, DC : ACS Publicationseng
dc.relation.doihttps://doi.org/10.1021/acsami.1c09071
dc.relation.essn1944-8252
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subject.ddc540eng
dc.subject.ddc600eng
dc.subject.otherB. morieng
dc.subject.othermesenchymal stromal cellseng
dc.subject.othersilk fibroineng
dc.subject.othersubstrate mechanicseng
dc.subject.otherviscoelasticeng
dc.titleSilk Hydrogel Substrate Stress Relaxation Primes Mesenchymal Stem Cell Behavior in 2Deng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorIPFeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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