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dc.contributor.authorMarsico, Grazia
dc.contributor.authorChunseng, Jin,
dc.contributor.authorAbbah, Sunny A.
dc.contributor.authorBrauchle, Eva M.
dc.contributor.authorThomas, Dilip
dc.contributor.authorRebelo, Ana Lúcia
dc.contributor.authorOrbanic, Doriana
dc.contributor.authorChantepie, Sandrine
dc.contributor.authorContessotto, , Paolo
dc.contributor.authorPapy Garcia, Dulce
dc.contributor.authorRodríguez Cabello, José Carlos 
dc.contributor.authorKilcoyne, Michelle
dc.contributor.authorSchenke, Layland, K.
dc.contributor.authorKarlsson, N.G.
dc.contributor.authorMcCullagh, Karl J.A.
dc.contributor.authorPandit, Abhay
dc.date.accessioned2022-07-12T07:36:33Z
dc.date.available2022-07-12T07:36:33Z
dc.date.issued2021
dc.identifier.citationBiomaterials, 2021, vol. 269, p. 120641es
dc.identifier.issn0142-9612es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/53893
dc.descriptionProducción Científicaes
dc.description.abstractCritical limb ischemia (CLI) is characterized by the impairment of microcirculation, necrosis and inflammation of the muscular tissue. Although the role of glycans in mediating inflammation has been reported, changes in the glycosylation following muscle ischemia remains poorly understood. Here, a murine CLI model was used to show the increase of high mannose, α-(2, 6)-sialic acid and the decrease of hybrid and bisected N-glycans as glycosylation associated with the ischemic environment. Using this model, the efficacy of an elastin-like recombinamers (ELR) hydrogel was assessed. The hydrogel modulates key angiogenic signaling pathways, resulting in capillary formation, and ECM remodeling. Arterioles formation, reduction of fibrosis and anti-inflammatory macrophage polarization wa also induced by the hydrogel administration. Modulation of glycosylation was observed, suggesting, in particular, a role for mannosylation and sialylation in the mediation of tissue repair. Our study elucidates the angiogenic potential of the ELR hydrogel for CLI applications and identifies glycosylation alterations as potential new therapeutic targets.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherElsevieres
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.classificationIschemiaes
dc.subject.classificationGlycosylationes
dc.subject.classificationAngiogenesises
dc.titleElastin-like hydrogel stimulates angiogenesis in a severe model of critical limb ischemia (CLI): An insight into the glyco-host responsees
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2020 The Author(s)es
dc.identifier.doi10.1016/j.biomaterials.2020.120641es
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0142961220308887es
dc.identifier.publicationfirstpage120641es
dc.identifier.publicationtitleBiomaterialses
dc.identifier.publicationvolume269es
dc.peerreviewedSIes
dc.description.projectThis work was funded by Science Foundation Ireland (SFI) and the European Regional Development Fund (Grant Number 13/RC/2073) AngioMatTrain Seventh Framework Programme Grant Agreement no.: 317304.es
dc.description.projectDeutsche Forschungsgemeinschaft (INST 2388/64-1, INST 2388/30-1)es
dc.description.projectMinistry of Science, Research and Arts of Baden Württemberg (Az.: SI-BW 01222-91, 33-729.55-3/214)es
dc.description.projectResearch in the mass spectrometry laboratory at the University of Goteborg was supported by EMBO short-term fellowships, in collaboration with the Swedish infrastructure for biological mass spectrometry (BioMS) supported by the Swedish Research Council.[ASTF- 7602-2018]es
dc.rightsAtribución 4.0 Internacional*
dc.rightsAtribución 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones
dc.subject.unesco24 Ciencias de la Vidaes
dc.subject.unesco22 Físicaes


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