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Biophys J, December 2002, p. 3162-3176, Vol. 83, No. 6


*Department of Chemical Engineering,
Graduate Program
in Molecular Biophysics, and
Department of Materials
Science and Engineering, The Johns Hopkins University, Baltimore,
Maryland 21218 USA
This paper introduces the method of live-cell
multiple-particle-tracking microrheology (MPTM), which quantifies the
local mechanical properties of living cells by monitoring the Brownian motion of individual microinjected fluorescent particles. Particle tracking of carboxylated microspheres imbedded in the cytoplasm produce
spatial distributions of cytoplasmic compliances and
frequency-dependent viscoelastic moduli. Swiss 3T3 fibroblasts are
found to behave like a stiff elastic material when subjected to high
rates of deformations and like a soft liquid at low rates of
deformations. By analyzing the relative contributions of the
subcellular compliances to the mean compliance, we find that the
cytoplasm is much more mechanically heterogeneous than reconstituted
actin filament networks. Carboxylated microspheres embedded in
cytoplasm through endocytosis and amine-modified polystyrene
microspheres, which are microinjected or endocytosed, often show
directed motion and strong nonspecific interactions with cytoplasmic
proteins, which prevents computation of local moduli from the
microsphere displacements. Using MPTM, we investigate the mechanical
function of
-actinin in non-muscle cells:
-actinin-microinjected
cells are stiffer and yet mechanically more heterogeneous than control
cells, in agreement with models of reconstituted cross-linked actin
filament networks. MPTM is a new type of functional microscopy that can
test the local, rate-dependent mechanical and ultrastructural
properties of living cells.
Biophys J, December 2002, p. 3162-3176, Vol. 83, No. 6
© 2002 by the Biophysical Society 0006-3495/02/12/3162/15 $2.00
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