4.4 Article Proceedings Paper

Force spectroscopy of hepatocytic extracellular matrix components

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ULTRAMICROSCOPY
卷 109, 期 8, 页码 942-947

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ELSEVIER
DOI: 10.1016/j.ultramic.2009.03.007

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Atomic force microscopy; Force spectroscopy; Hepatocyte; Extracellular matrix

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We present atomic force microscopy and force spectroscopy data of live hepatocytes (HEPG2/C3A liver cell line) grown in Eagle's Minimum Essential Medium, a complex solution of salts and amino acids commonly used for cell culture. Contact-mode imaging and force spectroscopy of this system allowed correlation of cell morphology and extracellular matrix (ECM) properties with substrate properties. Force spectroscopy analysis of cellular footprints indicated that the cells secrete large polymers (e.g., 3.5 mu m contour length and estimated MW 1000 kDa) onto their substrate surface. Although definitive identification of the polymers has not yet been achieved, fluorescent-labeled antibody staining has specified the presence of ECM proteins such as collagen and laminin in the cellular footprints. The stretched polymers appear to be much larger than single molecules of known ECM components, such as collagen and heparan sulfate proteoglycan, thus suggesting that the cells create larger entangled, macromolecular structures from smaller components. There is strong evidence which suggests that the composition of the ECM is greatly influenced by the hydrophobicity of the substrate surface, with preferential production and/or adsorption of larger macromolecules on hydrophobic surfaces. (c) 2009 Elsevier B.V. All rights reserved.

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