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Microelastic properties of lung cell-derived extracellular matrix

Patricia A. Soucya, Jeffery Werbinb, William Heinzc, Jan H. Hohd1, Lewis H. Romerae1Corresponding Author Informationemail address

Received 3 March 2010; received in revised form 18 July 2010; accepted 19 July 2010. published online 26 July 2010.
Corrected Proof

Abstract 

The mechanical properties of the extracellular microenvironment regulate cell behavior, including migration, proliferation and morphogenesis. Although the elastic moduli of synthetic materials have been studied, little is known about the properties of naturally produced extracellular matrix. Here we have utilized atomic force microscopy to characterize the microelastic properties of decellularized cell-derived matrix from human pulmonary fibroblasts. This heterogeneous three-dimensional matrix had an average thickness of 5±0.4μm and a Young’s modulus of 105±14Pa. Ascorbate treatment of the lung fibroblasts prior to extraction produced a twofold increase in collagen I content, but did not affect the stiffness of the matrices compared with matrices produced in standard medium. However, fibroblast-derived matrices that were crosslinked with glutaraldehyde demonstrated a 67% increase in stiffness. This work provides a microscale characterization of fibroblast-derived matrix mechanical properties. An accurate understanding of native three-dimensional extracellular microenvironments will be essential for controlling cell responses in tissue engineering applications.

a Departments of Biomedical Engineering and Anesthesiology and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA

b Department of Biophysics, Johns Hopkins University School of Medicine, Baltimore, MD, USA

c Intelligent Substrates Inc., Baltimore, MD, USA

d Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, MD, USA

e Departments of Cell Biology, Pediatrics, and Center for Cell Dynamics, Johns Hopkins University School of Medicine, Baltimore, MD, USA

Corresponding Author InformationCorresponding author.

1 These authors contributed equally to this work.

PII: S1742-7061(10)00341-7

doi:10.1016/j.actbio.2010.07.021