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Translation of collagen ultrastructure to biomaterial fabrication for material-independent but highly efficient topographic immunomodulation

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-256381
  • Supplement-free induction of cellular differentiation and polarization solely through the topography of materials is an auspicious strategy but has so far significantly lagged behind the efficiency and intensity of media-supplementation-based protocols. Consistent with the idea that 3D structural motifs in the extracellular matrix possess immunomodulatory capacity as part of the natural healing process, it is found in this study that human-monocyte-derived macrophages show a strong M2a-like prohealing polarization when cultured on type ISupplement-free induction of cellular differentiation and polarization solely through the topography of materials is an auspicious strategy but has so far significantly lagged behind the efficiency and intensity of media-supplementation-based protocols. Consistent with the idea that 3D structural motifs in the extracellular matrix possess immunomodulatory capacity as part of the natural healing process, it is found in this study that human-monocyte-derived macrophages show a strong M2a-like prohealing polarization when cultured on type I rat-tail collagen fibers but not on collagen I films. Therefore, it is hypothesized that highly aligned nanofibrils also of synthetic polymers, if packed into larger bundles in 3D topographical biomimetic similarity to native collagen I, would induce a localized macrophage polarization. For the automated fabrication of such bundles in a 3D printing manner, the strategy of “melt electrofibrillation” is pioneered by the integration of flow-directed polymer phase separation into melt electrowriting and subsequent selective dissolution of the matrix polymer postprocessing. This process yields nanofiber bundles with a remarkable structural similarity to native collagen I fibers, particularly for medical-grade poly(ε-caprolactone). These biomimetic fibrillar structures indeed induce a pronounced elongation of human-monocyte-derived macrophages and unprecedentedly trigger their M2-like polarization similar in efficacy as interleukin-4 treatment.zeige mehrzeige weniger

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Autor(en): Matthias RymaORCiD, Tina TylekORCiD, Julia Liebscher, Carina BlumORCiD, Robin Fernandez, Christoph Böhm, Wolfgang Kastenmüller, Georg Gasteiger, Jürgen GrollORCiD
URN:urn:nbn:de:bvb:20-opus-256381
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Medizinische Fakultät / Abteilung für Funktionswerkstoffe der Medizin und der Zahnheilkunde
Medizinische Fakultät / Institut für Systemimmunologie
Sprache der Veröffentlichung:Englisch
Titel des übergeordneten Werkes / der Zeitschrift (Englisch):Advanced materials
Erscheinungsjahr:2021
Band / Jahrgang:33
Heft / Ausgabe:33
Aufsatznummer:2101228
Originalveröffentlichung / Quelle:Advanced materials (2021) 33:33, 2101228. https://doi.org/10.1002/adma.202101228
DOI:https://doi.org/10.1002/adma.202101228
Allgemeine fachliche Zuordnung (DDC-Klassifikation):6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Freie Schlagwort(e):biofabrication; extracellular matrix; immunomodulation; macrophages; melt electrofibrillation; melt electrowriting
Datum der Freischaltung:21.02.2022
EU-Projektnummer / Contract (GA) number:617989
OpenAIRE:OpenAIRE
Lizenz (Deutsch):License LogoCC BY-NC-ND: Creative-Commons-Lizenz: Namensnennung, Nicht kommerziell, Keine Bearbeitungen 4.0 International