Changes in cell shape and volume are believed to play a role in the pr
ocess of mechanical signal transduction by chondrocytes in articular c
artilage. One proposed pathway through which chondrocyte deformation m
ay be transduced to an intracellular signal is through cytoskeletally
mediated deformation of intracellular organelles, and more specificall
y, of the cell nucleus. In this study, confocal scanning laser microsc
opy was used to perform in situ three-dimensional morphometric analyse
s of the nuclei of viable chondrocytes during controlled compression o
f articular cartilage explants from the canine patellofemoral groove.
Unconfined compression of the tissue to a 15% surface-to-surface strai
n resulted in a significant decrease of chondrocyte height and volume
by 14.7 +/- 6.4 and 11.4 +/- 8.4%, respectively, and of nuclear height
and volume by 8.8 +/- 6.2% and 9.8 +/- 8.8%, respectively. Disruption
of the actin cytoskeleton using cytochalasin D altered the relationsh
ip between matrix deformation and changes in nuclear height and shape,
but not volume. The morphology and deformation behavior of the chondr
ocytes were not affected by cytochalasin treatment. These results sugg
est that the actin cytoskeleton plays an important role in the link be
tween compression of the extracellular matrix and deformation of the c
hondrocyte nuclei and imply that chondrocytes and their nuclei undergo
significant changes in shape and volume in vivo.