2006 APS March Meeting
Monday–Friday, March 13–17, 2006;
Baltimore, MD
Session Z4: Biopolymers
11:15 AM–2:15 PM,
Friday, March 17, 2006
Baltimore Convention Center
Room: 308
Sponsoring
Units:
DPOLY DBP
Chair: Michael Lang and Zuowei Wang, University of North Carolina
Abstract ID: BAPS.2006.MAR.Z4.2
Abstract: Z4.00002 : Cellular Force, and Geometry Sensing (Over Time) Can Detect Matrix Rigidity: Local Modules Produce Global Signals
11:51 AM–12:27 PM
Preview Abstract
Abstract
Author:
Michael Sheetz
(Columbia University)
The shape and behavior of mammalian cells is defined by an
interplay between
extracellular signals and the cellular responses. Although the
chemical
nature of the external signals is important, there is a growing
realization
that the physical aspects of the external environment are equally
important.
In particular, the stresses, rigidity and form of the external
environment
have major effects on cell behavior. Of particular importance is
rigidity
since cancerous cells can often grow on soft agar or in a fluid
phase
without force production. For most mammalian cells there are
relatively few
types of motility that are evident from quantitative analyses of
rapidly
spreading fibroblasts (Dubin-Thaler et al., Biophys. J.
86:1794-1806, 2004).
One motile phase that we have studied extensively involves periodic
contractions (24 s period) in local regions of the leading edge
of the cell
(Giannone et al., Cell, 116:431-443, 2004). The periodic signal
is carried
radially from the cell edge toward the center and is part of a
general
mechanism for rigidity-directed movement and pathfinding. Another
motile
phase involves the movement of individual collagen fibers in a
hand-over-hand fashion (Meshel et al., Nature Cell Biol.
7:157-164, 2005)
where the form of the fiber is being sensed. Rigidity and form
sensing in
these systems is dependent upon the cytoskeleton and force-dependent
tyrosine phosphorylation through oncogenes (Sawada and Sheetz, J
Cell Biol.
156:609-15, 2002; Tamada et al., Developmental Cell, 7:706-718,
2004).
Recent studies indicate that the cell rigidity sensing occurs
preferentially
at the leading edges of moving cells and involves forces of 10-20 pN
generated by displacements of 50-100 nm (Jiang et al., Biophys J.
In Press).
We will discuss how cells organize motility tools in motile phases
(D\"{o}bereiner et al., Phys. Rev. Letters. 93:108105-1-4, 2004)
in a
dialogue with the environment to define cell morphology and
behavior over
time..
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2006.MAR.Z4.2