Introduction: Chondrocytes in articular cartilage utilize mechanical signal
s to regulate their metabolic activity. A fundamental step in determining t
he role of various biophysical factors in this process is to characterize t
he local mechanical environment of the chondrocyte under physiological load
ing.
Methods: A combined experimental and theoretical approach was used to quant
ify the in-situ mechanical environment of the chondrocyte. The mechanical p
roperties of enzymatically-isolated chondrocytes and their pericellular mat
rix (PCM) were determined using micropipette aspiration. The values were us
ed in a finite element model of the chondron (the chondrocyte and its PCM)
within articular cartilage to predict the stress-strain and fluid flow micr
oenvironment of the cell. The theoretical predictions were validated using
three-dimensional confocal microscopy of chondrocyte deformation in situ.
Results: Chondrocytes were found to behave as a viscoelastic solid material
with a Young's modulus of approximately 0.6 kPa. The elastic modulus of th
e PCM was significantly higher than that of the chondrocyte, but several or
ders of magnitude lower than that of the extracellular matrix. Theoretical
modeling of cell-matrix interactions suggests the mechanical environment of
the chondrocyte is highly non-uniform and is dependent on the viscoelastic
properties of the PCM. Excellent agreement was observed between the theore
tical predictions and the direct measurements of chondrocyte deformation, b
ut only if the model incorporated the PCM.
Conclusions: These findings imply that the PCM plays a functional biomechan
ical role in articular cartilage, and alterations in PCM properties with ag
ing or disease will significantly affect the biophysical environment of the
chondrocyte.