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Issue title: Selected Presentations held at the 34th Conference of the German Society for Clinical Microcirculation and Hemorheology, Regensburg, Germany, 27–28 November, 2015
Guest editors: L. Prantl, E.M. Jung and F. Jung
Article type: Research Article
Authors: Sievers, Henriekea; * | Hirschberg, Ruth M.b | Hiebl, Bernhardc | Hünigen, Hanaa | Plendl, Johannaa
Affiliations: [a] Institute of Veterinary Anatomy, Department of Veterinary Medicine, Freie Universität Berlin, Germany | [b] SFB 1112, Institute of Chemistry and Biochemistry - Physical and Theoretical Chemistry, Department of Biology, Chemistry and Pharmacy, Freie Universität Berlin, Germany | [c] Center for Medical Basic Research, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany
Correspondence: [*] Corresponding author: Henrieke Sievers, Institute of Veterinary Anatomy, Department of Veterinary Medicine, Freie Universität Berlin, Koserstraße 20, 14195 Berlin, Germany. Tel.: +49 30 83853560; Fax: +49 30 83853480; E-mail: [email protected]
Abstract: Human microvascular ECs from the neonatal foreskin of two donors purchased from one distributor were used in an angiogenesis assay under the same culture conditions. Different angiogenic potency was apparent in these two batches (ECang and ECnon-ang). During the cultivation period of three weeks, ECang ran through all stages of angiogenesis starting from proliferation to migration up to the formation of three-dimensional capillary-like structures. Despite of expression of endothelial markers, ECnon-ang showed excessive intracellular storage of lipids in form of multilamellar bodies and decreased angiogenic potency in contrast to its counterpart, ECang. Results indicate that lipid metabolism differs in ECang versus ECnon-ang. This study points up that these differences are based on the different donors and presents a novel and valuable model for the study of mechanisms of atherosclerosis in endothelial cells in vitro.
Keywords: Foreskin, fetal bovine serum, multilamellar bodies, atherosclerosis
DOI: 10.3233/CH-152002
Journal: Clinical Hemorheology and Microcirculation, vol. 61, no. 2, pp. 367-383, 2015
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