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Am J Physiol Heart Circ Physiol 294: H532-H540, 2008. First published October 26, 2007; doi:10.1152/ajpheart.00649.2007
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INNOVATIVE METHODOLOGY

A simple device to apply equibiaxial strain to cells cultured on flexible membranes

Obaida R. Rana,1 Carsten Zobel,2 Esra Saygili,2 Klara Brixius,2 Felix Gramley,1 Thomas Schimpf,1 Karl Mischke,1 Dirk Frechen,1 Christian Knackstedt,1 Robert H. G. Schwinger,3 Patrick Schauerte,1 and Erol Saygili1

1Department of Cardiology, University Rheinisch-Westfaelische Technische Hochschule Aachen, Aachen; 2Laboratory of Muscle Research and Molecular Cardiology, Department of Internal Medicine III, University of Cologne, Cologne; and 3Medical Clinic II, Klinikum Weiden, Weiden, Germany

Submitted 5 June 2007 ; accepted in final form 24 October 2007

The biomechanical environment to which cells are exposed is important to their normal growth, development, interaction, and function. Accordingly, there has been much interest in studying the role of biomechanical forces in cell biology and pathophysiology. This has led to the introduction and even commercialization of many experimental devices. Many of the early devices were limited by the heterogeneity of deformation of cells cultivated in different locations of the culture plate membranes and were also attached with complicated technical/electronic efforts resulting in a restriction of the reproducibility of these devices. The objective of this study was to design and build a simple device to allow the application of dose-dependent homogeneous equibiaxial static stretch to cells cultured on flexible silicone membranes to investigate biological and biomedical questions. In addition, cultured neonatal rat atrial cardiomyocytes were stretched with the proposed device with different strain gradients. For the first time with this study we could demonstrate that stretch up to 21% caused dose-dependent changes in biological markers such as the calcineurin activity, modulatory calcineurin-interacting protein-1, voltage-gated potassium channel isoform 4.2, and voltage-gated K+ channel-interacting proteins-2 gene expression and transient outward potassium current densities but not the protein-to-DNA ratio and atrial natriuretic peptide mRNA. With both markers mentioned last, dose-dependent stretch alterations could only be achieved with stretch up to 13%. The simple and low-cost device presented here might be applied to a wide range of experimental settings in different fields of research.

equibiaxial stretch; hypertrophy; calcineurin



Address for reprint requests and other correspondence: O. R. Rana, Univ. Hospital RWTH Aachen, Dept. I of Internal Medicine, Division of Cardiology, Pulmonary and Vascular Diseases, Pauwelsstr. 30, D-52074 Aachen, Germany (e-mail: orana{at}ukaachen.de)







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