Ju. Yoo et B. Johnstone, THE ROLE OF OSTEOCHONDRAL PROGENITOR CELLS IN FRACTURE REPAIR, Clinical orthopaedics and related research, (355), 1998, pp. 73-81
The repair of a fracture necessarily entails synthesis of osseous tiss
ue requiring the transformation of undifferentiated osteochondral prog
enitor cells to mature osteoblasts and chondrocytes, Owen and Friedens
tein proposed that there are stem cells for all mesenchymal tissues, r
esident in bone marrow throughout life, that have a lineage comparable
to that described for hematopoiesis. Subsequent with this initial stu
dy, marrow derived and periosteal derived progenitor cells have been s
hown to produce bone and cartilage in numerous in vivo and in vitro st
udies. The differentiation process appears to depend heavily on the in
fluences of numerous cytokines, especially the transforming growth fac
tor beta superfamily, Initial cartilage formation from progenitor cell
s is important in any secondary fracture repair. In the in vitro study
of chondrogenesis, the marrow derived progenitor cells were shown to
differentiate into their terminal phenotype, the hypertrophic chondroc
yte, as indicated by the detection of Type X collagen messenger ribonu
cleic acid and protein. A concomitant elevation in the alkaline phosph
atase level suggests that these cells are ready to mineralize. Despite
the importance of these cells in fracture repair, the characterizatio
n of these cells and the mechanism of their differentiation have only
begun to be explored.