Small defects of unfractured bone are believed to heal without a carti
laginous intermediate. We have determined the ex-tent of cartilage pro
duction in an experimental model of metaphyseal bone repair involving
defects in both cortical and cancellous bone, but no fracture. Norther
n analyses revealed the presence of mRNAs for type X and II collagens
in the repair tissue. Immunohistology confirmed subperiosteal depositi
on of both collagen types adjacent to the defect. While the mRNAs for
the two collagen types peaked by one week of defect healing, immunodet
ectable type X collagen was not observed until the second week. The da
ta suggest that reactivity of periosteum and activation of chondrogene
sis and subsequent endochondral ossification programs are involved in
murine bone repair regardless of defect type.