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Am J Physiol Cell Physiol 288: C72-C80, 2005. First published September 22, 2004; doi:10.1152/ajpcell.00056.2004
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PROTEIN AND VESICLE TRAFFICKING, CYTOSKELETON

Cell stiffness and receptors: evidence for cytoskeletal subnetworks

Hayden Huang,1 Jeremy Sylvan,1 Maxine Jonas,2 Rita Barresi,3 Peter T. C. So,2 Kevin P. Campbell,3 and Richard T. Lee1

1Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Cambridge; 2Biological Engineering Division, Massachusetts Institute of Technology, Cambridge, Massachusetts; and 3Department of Physiology and Biophysics and Department of Neurology, Howard Hughes Medical Institute, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, Iowa

Submitted 27 January 2004 ; accepted in final form 16 September 2004

Viscoelastic models of cells often treat cells as homogeneous objects. However, studies have demonstrated that cellular properties are local and can change dramatically on the basis of the location probed. Because membrane receptors are linked in various ways to the intracellular space, with some receptors linking to the cytoskeleton and others diffusing freely without apparent linkages, the cellular physical response to mechanical stresses is expected to depend on the receptor engaged. In this study, we tested the hypothesis that cellular mechanical stiffness as measured via cytoskeletally linked receptors is greater than stiffness measured via receptors that are not cytoskeletally linked. We used a magnetic micromanipulator to apply linear stresses to magnetic beads attached to living cells via selected receptors. One of the receptor classes probed, the dystroglycan receptors, is linked to the cytoskeleton, while the other, the transferrin receptors, is not. Fibronectin-coated beads were used to test cellular mechanical properties of the cytoskeleton without membrane dependence by allowing the beads to endocytose. For epithelial cells, transferrin-dependent stiffness and endocytosed bead-dependent stiffness were similar, while dystroglycan-dependent stiffness was significantly lower. For smooth muscle cells, dystroglycan-dependent stiffness was similar to the endocytosed bead-dependent stiffness, while the transferrin-dependent stiffness was lower. The conclusion of this study is that the measured cellular stiffness is critically influenced by specific receptor linkage and by cell type and raises the intriguing possibility of the existence of separate cytoskeletal networks with distinct mechanical properties that link different classes of receptors.

magnetic micromanipulator; dystroglycan; transferrin



Address for reprint requests and other correspondence: H. Huang, 65 Landsdowne St., Rm. 283, Cambridge, MA 02139







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