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Issue title: Selected papers of the 18th European Conference for Clinical Hemorheology and Microcirculation (ESCHM), 5-8 June, 2016, Lisbon, Portugal
Article type: Research Article
Authors: Krüger-Genge, A.a | Fuhrmann, R.b | Jung, F.a; * | Franke, R.P.b
Affiliations: [a] Institute of Biomaterial Science and Berlin-Brandenburg Center for Regenerative Therapies, Helmholtz-Zentrum Geesthacht, Teltow, Germany | [b] Abteilung Biomaterialien, Zentralinstitut für Biomedizinische Technik, Universität Ulm, Ulm, Germany
Correspondence: [*] Corresponding author: F. Jung, Institute of Biomaterial Science and Berlin-Brandenburg Center for Regenerative Therapies, Helmholtz-Zentrum Geesthacht, Teltow, Germany. Tel.: +03328 352 269; Fax: +03328 352 452; E-mail: [email protected].
Abstract: The endothelialization of cardiovascular prostheses is known to improve their haemocompatibility. As such body-foreign materials often do not endothelialize spontaneously. A lot of in vitro studies are ongoing how endothelialization of biomaterials can be improved. In this study the influence of different components of a tissue-typical extracellular matrix (ECM) like laminin, fibronectin or gelatin on the formation of an endothelial cell monolayer and on the shear resistance of adherent cells on these substrates was studied. The study revealed that the density of human venous endothelial cells (HUVEC) monolayers differed markedly between cells grown on a natural ECM and cells grown on singularized components of an ECM (p < 0.001). Only HUVEC grown on laminin showed similar densities and a stress fiber pattern comparable to HUVEC grown on the ECM. HUVEC grown on gelatin- or fibronectin-coated coverslips were less firmly attached to the substrate; frequently individual HUVEC and even groups of cells detached. Concluding it seems that coating of implants with laminin supports the formation of shear resistant endothelial cell (EC) monolayer - superior to other ECM components.
Keywords: HUVEC, extracellular matrix, laminin, fibronectin, gelatin
DOI: 10.3233/CH-168051
Journal: Clinical Hemorheology and Microcirculation, vol. 64, no. 4, pp. 867-874, 2016
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