Fibroblasts embedded in the amorphous healing tissue matrix of ligaments mi
grate into damaged sites during the inflammatory process that precedes the
formation of new connective tissue after ligament injury. Cell motility inv
olved in this migration is strongly influenced by cellular adhesion to prot
eins of the extracellular matrix. The adhesion mechanism of interest in thi
s study is the attachment of fibroblasts from the anterior cruciate and med
ial collateral ligaments to types I and III collagen, two fibrillar collage
ns secreted by fibroblasts during tissue repair. Types I and III collagen c
onstitute a major portion of these ligaments and are assembled by fibroblas
ts into long cable-like fibrils in the extracellular space. Tn this study,
a micropipette aspiration technique was used to measure the force required
to separate fibroblasts of the anterior cruciate and medial collateral liga
ments from substrates composed of type I or III collagen, each at a concent
ration of 2 or 5 mu g/ml. Approximately 1,200 fibroblasts from the anterior
cruciate ligament and 1,600 from the medial collateral ligament were used,
and the adhesion force and area of these cells were determined. Fibroblast
s from the anterior cruciate ligament exhibited greater adhesion force than
did those from the medial collateral ligament for all concentrations of ty
pes I and III collagen. In addition, the adhesiveness of fibroblasts from b
oth ligaments was dependent on seeding time for all experimental conditions
. To determine the adhesiveness per unit area, defined here as the adhesion
strength, the adhesion force was normalized by the adhesion area. At early
seeding times (15-45 minutes), fibroblasts from the anterior cruciate liga
ment exhibited greater adhesion strength on surfaces coated with type-I col
lagen than did those from the medial collateral ligament. However, for both
collagen substrates, adhesion strength for fibroblasts from the anterior c
ruciate ligament decreased with seeding time whereas that for fibroblasts f
rom the medial collateral ligament remained relatively constant for all see
ding periods (15-75 minutes).