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Biomimetic mineralization promotes viability and differentiation of human mesenchymal stem cells in a perfusion bioreactor

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-285804
  • In bone tissue engineering, the design of 3D systems capable of recreating composition, architecture and micromechanical environment of the native extracellular matrix (ECM) is still a challenge. While perfusion bioreactors have been proposed as potential tool to apply biomechanical stimuli, its use has been limited to a low number of biomaterials. In this work, we propose the culture of human mesenchymal stem cells (hMSC) in biomimetic mineralized recombinant collagen scaffolds with a perfusion bioreactor to simultaneously provide biochemicalIn bone tissue engineering, the design of 3D systems capable of recreating composition, architecture and micromechanical environment of the native extracellular matrix (ECM) is still a challenge. While perfusion bioreactors have been proposed as potential tool to apply biomechanical stimuli, its use has been limited to a low number of biomaterials. In this work, we propose the culture of human mesenchymal stem cells (hMSC) in biomimetic mineralized recombinant collagen scaffolds with a perfusion bioreactor to simultaneously provide biochemical and biophysical cues guiding stem cell fate. The scaffolds were fabricated by mineralization of recombinant collagen in the presence of magnesium (RCP.MgAp). The organic matrix was homogeneously mineralized with apatite nanocrystals, similar in composition to those found in bone. X-Ray microtomography images revealed isotropic porous structure with optimum porosity for cell ingrowth. In fact, an optimal cell repopulation through the entire scaffolds was obtained after 1 day of dynamic seeding in the bioreactor. Remarkably, RCP.MgAp scaffolds exhibited higher cell viability and a clear trend of up-regulation of osteogenic genes than control (non-mineralized) scaffolds. Results demonstrate the potential of the combination of biomimetic mineralization of recombinant collagen in presence of magnesium and dynamic culture of hMSC as a promising strategy to closely mimic bone ECM.zeige mehrzeige weniger

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Autor(en): Gloria Belén Ramírez-Rodríguez, Ana Rita Pereira, Marietta Herrmann, Jan Hansmann, José Manuel Delgado-López, Simone Sprio, Anna Tampieri, Monica Sandri
URN:urn:nbn:de:bvb:20-opus-285804
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Medizinische Fakultät / Lehrstuhl für Orthopädie
Sprache der Veröffentlichung:Englisch
Titel des übergeordneten Werkes / der Zeitschrift (Englisch):International Journal of Molecular Sciences
ISSN:1422-0067
Erscheinungsjahr:2021
Band / Jahrgang:22
Heft / Ausgabe:3
Aufsatznummer:1447
Originalveröffentlichung / Quelle:International Journal of Molecular Sciences 2021, 22(3), 1447; https://doi.org/10.3390/ijms22031447
DOI:https://doi.org/10.3390/ijms22031447
Sonstige beteiligte Institutionen:IZKF Nachwuchsgruppe Geweberegeneration für muskuloskelettale Erkrankungen
Allgemeine fachliche Zuordnung (DDC-Klassifikation):6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Freie Schlagwort(e):apatite nanoparticles; collagen; human mesenchymal stem cell; magnesium; osteogenesis; perfusion bioreactor; scaffold
Datum der Freischaltung:11.07.2023
Datum der Erstveröffentlichung:01.02.2021
EU-Projektnummer / Contract (GA) number:607051
OpenAIRE:OpenAIRE
Lizenz (Deutsch):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International