A growth factor-based strategy recently has been shown to induce the intrin
sic repair of partial-thickness articular cartilage lesions, thereby obviat
ing the need for transplanting cells or tissue. It was the purpose of the c
urrent study to ascertain whether this principle could be applied to full-t
hickness articular cartilage defects created in adult rabbits and mature mi
niature pigs. The transforming growth factor-beta1 contained within the aut
hors' chondrogenic matrix-complex proved to be potent in its osteogenic cap
acity when liberated into the bone compartment of such lesions, inducing th
e rapid upgrowth of osseous tissue and vascular buds into the cartilage com
partment. This is an unwanted response that must be prevented. A cell and b
lood vessel-excluding membrane (Millipore (R) in rabbits and Goretex (R) in
miniature pigs) was inserted at the interface between cartilage and bone c
ompartments, both of which were filled at the appropriate juncture with the
chondrogenic matrix-complex. These structural barriers were effective in o
bstructing the upgrowth of blood vessels into the cartilage compartment and
in preventing the osteogenic tissue differentiation attributable to the pr
esence of a vasculature.