|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Articles in PresS, published online ahead of print June 26, 2002
Am J Physiol Cell Physiol, 10.1152/ajpcell.00169.2002
Submitted on April 12, 2002
Accepted on June 19, 2002
1 Physiology Program, Harvard School of Public Health, Boston, MA, USA; Physical Chemistry, Rugjer Boskovic Institute, Zagreb, Croatia (Hrvatska)
2 Physiology Program, Harvard School of Public Health, Boston, MA, USA
* To whom correspondence should be addressed. E-mail: tolic{at}nbi.dk.
Tractions that cells exert on their substrates are essential in cell spreading, migration and contraction. These tractions can be determined by plating the cells on a flexible gel, and measuring the deformation of the gel using fluorescent beads embedded just below the surface of the gel. In this paper we describe the Image Correlation Method (ICM) optimized for determining the displacement field of the gel under a contracting cell. For the calculation of the traction field from the displacement field we use the recently developed method of Fourier Transform Traction Cytometry (FTTC). The ICM and FTTC methods are applied to human airway smooth muscle cells during stimulation with the contractile agonist histamine or the relaxing agonist isoproterenol. The overall intensity of the cell contraction (the median traction magnitude, the energy transferred from the cell to the gel, and the net contractile moment) increased after activation with histamine, and decreased after treatment with isoproterenol. Cells exhibited regional differences in the time course of traction during the treatment. Both temporal evolution and magnitude of traction increase induced by histamine varied markedly among different cell protrusions, while the nuclear region showed the smallest response. These results suggest that intracellular mediators of cell adhesion and contraction respond to contractile stimuli with different rates and intensities in different regions of the cell.
This article has been cited by other articles:
![]() |
K. Ghosh, C. K. Thodeti, A. C. Dudley, A. Mammoto, M. Klagsbrun, and D. E. Ingber Tumor-derived endothelial cells exhibit aberrant Rho-mediated mechanosensing and abnormal angiogenesis in vitro PNAS, August 12, 2008; 105(32): 11305 - 11310. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Gavara, P. Roca-Cusachs, R. Sunyer, R. Farre, and D. Navajas Mapping Cell-Matrix Stresses during Stretch Reveals Inelastic Reorganization of the Cytoskeleton Biophys. J., July 1, 2008; 95(1): 464 - 471. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Gavara, R. Sunyer, P. Roca-Cusachs, R. Farre, M. Rotger, and D. Navajas Thrombin-induced contraction in alveolar epithelial cells probed by traction microscopy J Appl Physiol, August 1, 2006; 101(2): 512 - 520. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Huang, R. D. Kamm, and R. T. Lee Cell mechanics and mechanotransduction: pathways, probes, and physiology Am J Physiol Cell Physiol, July 1, 2004; 287(1): C1 - C11. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Stamenovic, B. Suki, B. Fabry, N. Wang, J. J. Fredberg, and J. E. Buy Rheology of airway smooth muscle cells is associated with cytoskeletal contractile stress J Appl Physiol, May 1, 2004; 96(5): 1600 - 1605. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. R. Polte, G. S. Eichler, N. Wang, and D. E. Ingber Extracellular matrix controls myosin light chain phosphorylation and cell contractility through modulation of cell shape and cytoskeletal prestress Am J Physiol Cell Physiol, March 1, 2004; 286(3): C518 - C528. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Hu, J. Chen, B. Fabry, Y. Numaguchi, A. Gouldstone, D. E. Ingber, J. J. Fredberg, J. P. Butler, and N. Wang Intracellular stress tomography reveals stress focusing and structural anisotropy in cytoskeleton of living cells Am J Physiol Cell Physiol, November 1, 2003; 285(5): C1082 - C1090. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |
| Visit Other APS Journals Online |