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    Por favor, use este identificador para citar o enlazar este ítem:https://uvadoc.uva.es/handle/10324/53893

    Título
    Elastin-like hydrogel stimulates angiogenesis in a severe model of critical limb ischemia (CLI): An insight into the glyco-host response
    Autor
    Marsico, Grazia
    Chunseng, Jin,
    Abbah, Sunny A.
    Brauchle, Eva M.
    Thomas, Dilip
    Rebelo, Ana Lúcia
    Orbanic, Doriana
    Chantepie, Sandrine
    Contessotto, , Paolo
    Papy Garcia, Dulce
    Rodríguez Cabello, José CarlosAutoridad UVA Orcid
    Kilcoyne, Michelle
    Schenke, Layland, K.
    Karlsson, N.G.
    McCullagh, Karl J.A.
    Pandit, Abhay
    Año del Documento
    2021
    Editorial
    Elsevier
    Descripción
    Producción Científica
    Documento Fuente
    Biomaterials, 2021, vol. 269, p. 120641
    Résumé
    Critical 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.
    Materias Unesco
    24 Ciencias de la Vida
    22 Física
    Palabras Clave
    Ischemia
    Glycosylation
    Angiogenesis
    ISSN
    0142-9612
    Revisión por pares
    SI
    DOI
    10.1016/j.biomaterials.2020.120641
    Patrocinador
    This 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.
    Deutsche Forschungsgemeinschaft (INST 2388/64-1, INST 2388/30-1)
    Ministry of Science, Research and Arts of Baden Württemberg (Az.: SI-BW 01222-91, 33-729.55-3/214)
    Research 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]
    Version del Editor
    https://www.sciencedirect.com/science/article/pii/S0142961220308887
    Propietario de los Derechos
    © 2020 The Author(s)
    Idioma
    eng
    URI
    https://uvadoc.uva.es/handle/10324/53893
    Tipo de versión
    info:eu-repo/semantics/publishedVersion
    Derechos
    openAccess
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    • BIOFORGE - Artículos de revista [89]
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