Chondrocytes in articular cartilage utilize mechanical signals in conjuncti
on with other environmental factors to regulate their metabolic activity. H
owever, the sequence of biomechanical and biochemical events involved in th
e process of mechanical signal transduction has not been fully deciphered.
A fundamental step in determining the role of various factors in regulating
chondrocyte activity is to characterize accurately the biophysical environ
ment within the tissue under physiological conditions of mechanical loading
. Microscopic imaging studies have revealed that chondrocytes as well as th
eir nuclei undergo shape and volume changes in a coordinated manner with de
formation of the tissue matrix. Through micromechanical experiments, it has
been shown that the chondrocyte behaves as a viscoelastic solid material w
ith a mechanical stiffness that is several orders of magnitude lower than t
hat of the cartilage extracellular matrix. These properties seem to be due
to the structure of the chondrocyte cytoskeleton, and in part, the viscoela
stic properties of the cell nucleus. The mechanical properties of the peric
ellular matrix that immediately surrounds the chondrocyte significantly dif
fer from those of the chondrocyte and the extracellular matrix, suggesting
that the pericellular matrix plays an important role in defining the mechan
ical environment of the chondrocyte. These experimentally measured values f
or cbondrocyte and cartilage mechanical properties have been used in combin
ation with theoretical constitutive modeling of the chondrocyte within arti
cular cartilage to predict the non-uniform and time-varying stress-strain a
nd fluid flow environment of the cell. The ultimate goal of these studies h
as been to elucidate the sequence of biomechanical and biochemical events t
hrough which mechanical stress influences chondrocyte activity in both heal
th and in disease.