The contractile force developed by fibroblasts has been studied by measurin
g the macroscopic contraction of porous collagen-GAG matrices over time. We
have identified the microscopic deformations developed by individual fibro
blasts which lead to the observed macroscopic matrix contraction. Observati
on of live cells attached to the matrix revealed that matrix deformation oc
curred as a result of cell elongation. The time dependence of the increase
in average fibroblast aspect ratio over time corresponded with macroscopic
matrix contraction, further linking cell elongation and matrix contraction.
The time dependence of average fibroblast aspect ratio and macroscopic mat
rix contraction was found to be the result of the stochastic nature of cell
elongation initiation and of the time required for cells to reach a final
morphology (2-4 h). The proposed micromechanics associated with observed bu
ckling or bending of individual struts of the matrix by cells may, in part,
explain the observation of a force plateau during macroscopic contraction.
These findings indicate that the macroscopic matrix contraction measured i
mmediately following cell attachment is related to the extracellular force
necessary to support cell elongation, and that macroscopic time dependence
is not directly related to microscopic deformation events. (C) 2001 Academi
c Press.