|
|
|
|
Vol. 19, Issue 5, 2051-2058, May 2008
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9039
Submitted September 18, 2007;
Revised February 6, 2008;
Accepted February 19, 2008
Monitoring Editor: Yu-Li Wang
In nested collagen matrices, human fibroblasts migrate from cell-containing dermal equivalents into surrounding cell-free outer matrices. Time-lapse microscopy showed that in addition to cell migration, collagen fibril flow occurred in the outer matrix toward the interface with the dermal equivalent. Features of this flow suggested that it depends on the same cell motile machinery that normally results in cell migration. Collagen fibril flow was capable of producing large-scale tissue translocation as shown by closure of a
1-mm gap between paired dermal equivalents in floating, nested collagen matrices. Our findings demonstrate that when fibroblasts interact with collagen matrices, tractional force exerted by the cells can couple to matrix translocation as well as to cell migration.
Address correspondence to: Frederick Grinnell (frederick.grinnell{at}utsouthwestern.edu)
This article has been cited by other articles:
![]() |
R. J. Bloom, J. P. George, A. Celedon, S. X. Sun, and D. Wirtz Mapping Local Matrix Remodeling Induced by a Migrating Tumor Cell Using Three-Dimensional Multiple-Particle Tracking Biophys. J., October 15, 2008; 95(8): 4077 - 4088. [Abstract] [Full Text] [PDF] |
||||