Chondrocyte adhesion to cartilage may play an important role in the repair
of articular defects by maintaining cells in positions where their biosynth
etic products can contribute to the repair process. The objective of this i
n vitro study was to determine the effect of the duration of seeding time o
n the ability of chondrocytes to resist detachment from cartilage when subj
ected to mechanical perturbation (fluid-induced shear stress). Suspensions
of adult bovine articular chondrocytes were prepared from primary, high-den
sity monolayer cultures and infused into a parallel-plate shear-flow chambe
r where they settled onto 50-mu m-thick sections of bovine articular cartil
age at a density of approximately 20,000 cells/cm(2). The chondrocytes were
seeded and allowed to attach to the cartilage surface for specific duratio
ns (5-40 minutes) in medium including 10% serum at 22 degrees C, after whic
h the cells were exposed to fluid flow induced shear stresses (6-90 Pa). Th
e fraction of detached cells at each shear stress was calculated from micro
scopic images. Shear stress was applied for 1 minute because this length of
time was sufficient to induce steady-state cell detachment. Increasing the
duration of cell seeding led to a more firm attachment of chondrocytes to
cartilage. After 9 minutes of seeding, 50% cell detachment was induced by g
ravitational force alone. After 40 minutes of seeding, 50% detachment requi
red 26 Pa of shear stress. Extrapolation of the data to account for the eff
ect of repeated applications of cell suspensions to an individual cartilage
substrate indicated that for a freshly prepared cartilage section, 50% det
achment was induced by gravity after 25 minutes of seeding and by 2.3 Pa of
shear stress after 40 minutes of seeding. The increase in resistance to sh
ear stress-induced cell detachment with increasing seeding duration suggest
s that it may be beneficial to allow chondrocytes to stabilize in the absen
ce of applied load for some time after chondrocyte transplantation for cart
ilage repair in vivo.