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Micro-Physiological-Systems enable investigation of hypoxia induced pathological processes in human aortic valve cells and tissues

 
: Winkelkotte, Maximilian; Schmieder, Florian; Behrens, Stephan; Salminger, Dominic; Jannasch, Anett; Matschke, Klaus; Tugtekin, Sems-Malte; Sonntag, Frank; Dittfeld, Claudia

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Current directions in biomedical engineering 7 (2021), Nr.2, S.45-48
ISSN: 2364-5504
Deutsche Stiftung für Herzforschung
F/08/18
Experimentelle Analyse des Einflusses der Hypoxie auf die Pathogenese von Aortenklappengewebe und daraus isolierter Zellkulturen in Mikrophysiologischen Systemen
Englisch
Zeitschriftenaufsatz, Elektronische Publikation
Fraunhofer IWS ()
Aortic valve stenosis; Micro physiological system; hypoxia; valvular interstitial cells; tissue viability

Abstract
Aortic valve (AV) stenosis is characterized by tissue fibrosis and calcification. Fibrous thickening can result in reduced tissue oxygen supply leading to pathological valvular interstitial cell (VIC) differentiation and calcification. Static 2D VIC cultures and animal models are limited in the ability to reflect human AV calcification. Culturing of VICs in micro-physiological-systems (MPS) in a pulsatile flow and the establishment of a modular AV tissue incubation chamber (TIC) are new approaches to evaluate pathophysiological processes of AV disease. Therefore, a MPS able to adjust hypoxic conditions was applied for VIC culture. A significant increase of mRNA-expression ofEGLN1 and HIF1α-regulated LDHA andHIF1α nuclear localisation were proven under hypoxia. AV tissue culture was established within a TIC and viability was monitored by Resazurin-reduction in the incubation medium and visualized by LDH-activity in tissue cryosections. Viability was compared between fluid and static incubated tissues revealing an advantageous effect of the fluidic assay condition. Consecutively, the application of MPSin AV research allows i) the investigation of VIC cultures with efficient oxygen regulation and ii) the culture of porcine or human AV tissues preserving viability and specifically reflecting in vivo parameters. These methods open up new possibilities beyond static 2D culture and facilitate a reduction of animal experiments in AV research.

: http://publica.fraunhofer.de/dokumente/N-644489.html