N. Matsumoto et al., EFFECT OF ALIGNMENT OF THE TRANSPLANTED GRAFT EXTRACELLULAR-MATRIX ONCELLULAR REPOPULATION AND NEWLY SYNTHESIZED COLLAGEN, Archives of orthopaedic and trauma surgery, 117(4-5), 1998, pp. 215-221
This study examines the effect of alignment of the transplanted graft
extracellular matrix on cellular repopulation and new collagen synthes
is. The lateral half of the patellar tendon was harvested as a tendon
graft from Lewis rats and frozen at -80 degrees C. In order to maintai
n the original alignment of the graft extracellular matrix, the graft
was transplanted to a same size defect in the patellar tendon of other
Lewis rats (group I). For controls, the graft was transplanted in a l
ax condition after excision of only the distal half of the lateral sid
e of a patellar tendon (group II). After transplantation, six animals
in each group were killed at 3, 7, 14, and 28 days. Cellular repopulat
ion was assessed by using fibrillar-actin (F-actin) labeling with rhod
amine-phalloidin. and new collagen synthesis was detected by means of
a polyclonal antibody against type III collagen aminopropeptide (pN co
llagen III). Collagen fibril profiles were observed under the transmis
sion electron microscope. On the 3rd day after transplantation, no spe
cific fluorescence was detected in either group. Specific labeling for
F-actin and pN collagen In, however, was observed at both ends of the
graft in both groups at I week and throughout the graft at 2 weeks af
ter transplantation. Consistent with the actin bundles' orientation, p
N collagen III was aligned parallel to the longitudinal axis of the gr
aft in group I. Collagen fibrils with a smaller diameter, mixed evenly
and everywhere with a larger diameter, increased gradually in group I
. However, smaller collagen fibrils in group II increased more slowly
and were distributed unevenly. In summary, the dense collagen arrangem
ent in the native patellar tendon determined the alignment of the repo
pulating cells, and the distribution of newly synthesized collagen mig
ht be affected by the actin cytoskeleton within the repopulating cells
.